U.S. patent application number 14/193184 was filed with the patent office on 2014-07-10 for low-viscosity liquid crystal compound.
This patent application is currently assigned to Chemgenesis Incorporated. The applicant listed for this patent is Chemgenesis Incorporated. Invention is credited to Ichiro Hijikuro, Yasuhiro Hiroki, Yutaka Ikeda, Satoshi Imuta, Takashi Takahashi, Jun Yamashita.
Application Number | 20140194536 14/193184 |
Document ID | / |
Family ID | 44195905 |
Filed Date | 2014-07-10 |
United States Patent
Application |
20140194536 |
Kind Code |
A1 |
Ikeda; Yutaka ; et
al. |
July 10, 2014 |
LOW-VISCOSITY LIQUID CRYSTAL COMPOUND
Abstract
The present invention relates to a liquid crystal compound that
can be used as a base for injection formulations. The present
invention provides an amphipathic compound having the following
general formula (I): ##STR00001## wherein X and Y each denotes a
hydrogen atom or together denote an oxygen atom, n denotes an
integer from 0 to 2, m denotes the integer 1 or 2, and R denotes a
hydrophilic group generated by removal of one hydroxyl group from
any one selected from the group consisting of glycerol, erythritol,
pentaerythritol, diglycerol, triglycerol, xylose, sorbitol,
ascorbic acid, glucose, galactose, mannose, dipentaerythritol,
maltose, mannitol, and xylitol; as well as a base for injection
formulations and depot formulation comprising the same.
Inventors: |
Ikeda; Yutaka; (Tokyo,
JP) ; Yamashita; Jun; (Tokyo, JP) ; Hijikuro;
Ichiro; (Tokyo, JP) ; Imuta; Satoshi; (Tokyo,
JP) ; Hiroki; Yasuhiro; (Tokyo, JP) ;
Takahashi; Takashi; (Tokyo, JP) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Chemgenesis Incorporated |
Tokyo |
|
JP |
|
|
Assignee: |
Chemgenesis Incorporated
Tokyo
JP
|
Family ID: |
44195905 |
Appl. No.: |
14/193184 |
Filed: |
February 28, 2014 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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13518932 |
Jun 25, 2012 |
8703922 |
|
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PCT/JP2010/073621 |
Dec 27, 2010 |
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14193184 |
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Current U.S.
Class: |
514/777 ;
514/772; 514/785; 514/786; 536/18.2; 536/4.1; 549/315; 554/223;
568/687; 568/909.5 |
Current CPC
Class: |
A61K 9/0019 20130101;
A61K 47/10 20130101; C09K 19/06 20130101; A61K 9/0024 20130101;
A61K 47/26 20130101; A61K 47/14 20130101; C07H 15/10 20130101; A61K
47/22 20130101; A61K 47/08 20130101 |
Class at
Publication: |
514/777 ;
554/223; 514/785; 514/786; 568/909.5; 514/772; 536/18.2; 568/687;
549/315; 536/4.1 |
International
Class: |
A61K 47/14 20060101
A61K047/14; A61K 47/22 20060101 A61K047/22; A61K 47/08 20060101
A61K047/08; A61K 47/10 20060101 A61K047/10; A61K 47/26 20060101
A61K047/26 |
Foreign Application Data
Date |
Code |
Application Number |
Dec 25, 2009 |
JP |
2009-295658 |
Claims
1. An amphipathic compound having the following general formula
(I): ##STR00164## wherein X and Y each denotes a hydrogen atom or
together denote an oxygen atom, n denotes the integer 0, m denotes
the integer 1 or 2, and R denotes a hydrophilic group generated by
removal of one hydroxyl group from any one selected from the group
consisting of glycerol, erythritol, pentaerythritol, diglycerol,
triglycerol, xylose, sorbitol, ascorbic acid, glucose, galactose,
mannose, dipentaerythritol, maltose, mannitol, and xylitol.
2. The compound according to claim 1, which has viscosity of 11.0
Pas or less as determined at 25.degree. C.
3. The compound according to claim 1, wherein X and Y together
denote an oxygen atom, and R denotes a hydrophilic group generated
by removal of one hydroxyl group from glycerol or diglycerol.
4. The compound according to claim 3, wherein the compound is
selected from the group consisting of:
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)glycerol,
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)diglycerol,
mono-O-(3,7,11-trimethyldodec-2-enoyl)glycerol, and
mono-O-(3,7,11-trimethyldodec-2-enoyl)diglycerol.
5. The compound according to claim 1, wherein R denotes a
hydrophilic group generated by removal of one hydroxyl group from
any one selected from the group consisting of erythritol,
pentaerythritol, triglycerol, xylose, sorbitol, ascorbic acid,
glucose, galactose, mannose, dipentaerythritol, maltose, mannitol,
and xylitol.
6. The compound according to claim 5, wherein the compound is
selected from the group consisting of:
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)erythritol,
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)pentaerythritol,
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-xylopyranoside,
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)erythritol,
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)pentaerythritol,
mono-O-(3,7,11-trimethyldodec-2-enoyl)erythritol,
mono-O-(3,7,11-trimethyldodec-2-enoyl)pentaerythritol,
1-O-(3,7,11-trimethyldodec-2-enyl)-D-xylopyranoside,
mono-O-(3,7,11-trimethyldodec-2-enyl)erythritol, and
mono-O-(3,7,11-trimethyldodec-2-enyl)pentaerythritol.
7. The compound according to claim 1, wherein the compound is:
mono-O-(3,7,11-trimethyldodec-2-enyl)glycerol, or
mono-O-(3,7,11-trimethyldodec-2-enyl)diglycerol.
8. A base for injection formulations, which comprises at least one
type of the compound according to claim 1.
9. A depot formulation, which comprises the base according to claim
8.
10. A composition comprising the compound according to claim 1 and
an active ingredient.
11. The composition according to claim 10, wherein the composition
further comprises an aqueous medium, and said amphipathic compound
forms a non-lamellar liquid crystal in the composition.
12. A method for administering an active ingredient to a subject,
comprising administering the composition according to claim 10,
wherein said amphipathic compound forms a non-lamellar liquid
crystal in a living body of the subject.
13. A method for administering an active ingredient to a subject,
comprising administering the composition according to claim 11,
wherein said amphipathic compound forms a non-lamellar liquid
crystal in a living body of the subject.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a Continuation of U.S. patent
application Ser. No. 13/518,932, filed on Jun. 25, 2012 which is a
national stage application filed under 35 USC .sctn.371 of
PCT/JP2010/073621, filed Dec. 27, 2010, which claims the benefit of
Japanese Patent Application No. 2009-295658, filed Dec. 25, 2009,
all of which are incorporated herein by reference in their
entireties.
FIELD OF THE INVENTION
[0002] The present invention relates to a liquid crystal compound
useful as a base for injection formulations.
BACKGROUND OF THE INVENTION
[0003] Amphipathic compounds having both hydrophilic and
hydrophobic groups within the same molecules spontaneously form
various shapes of molecular assemblies in water. Amphipathic
compounds form various molecular assemblies in water at the Krafft
temperature (TK; referred to as Krafft eutectic temperature, Krafft
point, or the like) or higher, as determined depending on the types
or concentrations thereof (Non-patent Document 1). Examples of such
molecular clusters include closed micelles (e.g., spherical micells
and rod micells) with hydrophilic groups oriented outward, closed
reversed micelles with hydrophobic groups oriented outward, sponge
phases wherein hydrophobic groups or hydrophilic groups of
amphipathic compounds are aligned facing each other in bilayer
membranes and the bilayer membranes are randomly connected, and
various lyotropic liquid crystal phases. Known examples of the
lyotropic liquid crystal phase include hexagonal liquid crystal and
reverse hexagonal liquid crystal wherein infinitely long
cylindrical clusters form a two-dimensional hexagonal lattice,
lamellar liquid crystal wherein bilayer membrane sheets are layered
at regular intervals in the direction of the Z axis, and cubic
liquid crystal having a three-dimensional lattice structure.
Amphipathic compounds forming liquid crystal are referred to as
liquid crystal compounds.
[0004] These molecular clusters, and amphipathic compounds forming
liquid crystal in particular, are used for various applications in
the fields of cosmetics, pharmaceutical products, and the like. For
example, drug delivery systems (DDS) using amphipathic compounds
are under active development. Various forms of drug delivery
carriers have been produced, including a drug delivery system
(Non-patent Document 2) in which a drug is embedded in an
intraliposomal aqueous phase or a lipid bilayer prepared from
lamellar liquid crystal (Patent Documents 1 and 2). In particular,
non-lamellar liquid crystal such as cubic liquid crystal or reverse
hexagonal liquid crystal has a high degree of structural stability
and is capable of stably retaining various drugs within itself, and
thus is attracting attention as a particularly useful drug delivery
carrier.
[0005] Meanwhile, most forms of cubic liquid crystal found in an
amphipathic compound/water system can remain stable only within a
narrow concentration range between other phase regions, such as an
aqueous micelle solution, hexagonal liquid crystal, lamellar liquid
crystal, and reverse hexagonal liquid crystal, which occupy large
areas on a two-component (amphipathic compound/water) phase diagram
(Non-patent Document 3). Thus, the cubic liquid crystal is used
with difficulty as a drug delivery carrier or the like. In recent
years, it has been reported that monoacylglycerols including
monoolein and phytantriols form "type II cubic liquid crystal"
wherein a cubic phase and an aqueous phase are adjacent to each
other on a two-component (amphipathic compound/water) phase
diagram. It has also been reported that the liquid crystal is
relatively stable even when it coexists with excess water. Thus,
application of the liquid crystal to a drug delivery system or the
like has been attempted (Non-patent Document 4). However, liquid
crystal formed by monoolein and the like has low stability at low
temperatures. Accordingly, an amphipathic compound capable of
forming cubic liquid crystal that exhibits high stability at low
temperatures (less than 6.degree. C.) has been developed and the
use of the liquid crystal in a sustained release formulation has
also been disclosed (Patent Document 3).
[0006] However, such liquid crystal compounds stably forming cubic
liquid crystal have high viscosity and thus do not allow the
compounds to pass through a thin injection needle (e.g., 30 gauge).
Hence, these liquid crystal compounds are problematic in that they
are used with difficulty as bases for injection formulations.
REFERENCES
Patent Documents
[0007] Patent Document 1: JP Patent Publication (Kohyo) No.
2002-505307 A [0008] Patent Document 2: JP Patent Publication
(Kokai) No. 2001-231845 A [0009] Patent Document 3: International
Patent Publication WO2006/043705
Non-Patent Documents
[0009] [0010] Non-Patent Document 1: Laughlin, R. G, "The Aqueous
Phase Behavior of Surfactants" (1994) Academic Press London, p.
106-117 [0011] Non-Patent Document 2: Lasic D. D., TIBTECH 16,
(1998) p. 307-321 [0012] Non-Patent Document 3: Fontell, K. Colloid
& Polymer Sci., 268 (1990) p. 264-285 [0013] Non-Patent
Document 4: Barauskas, J., Landh, T., Langmuir, (2003) 19, p.
9562-9565
SUMMARY OF THE INVENTION
Disclosure of the Invention
Problem to be Solved by the Invention
[0014] An object of the present invention is to provide a liquid
crystal compound that can be used as a base for injection
formulations.
Means for Solving the Problem
[0015] As a result of intensive studies to achieve the above
object, the present inventors have found that an amphipathic
compound having a predetermined general formula, in which long
chain unsaturated hydrocarbon is linked to polyhydric alcohol via
ester, ether, or glycosidic linkage, has particularly low
viscosity, and is capable of forming type II (water-in-oil)
non-lamellar liquid crystal useful as a drug delivery carrier in an
aqueous medium. Thus, the present inventors have completed the
present invention.
[0016] The present invention encompasses the following (1) to
(3).
[1] An amphipathic compound having the following general formula
(I):
##STR00002##
wherein X and Y each denotes a hydrogen atom or together denote an
oxygen atom, n denotes an integer from 0 to 2, m denotes the
integer 1 or 2, and R denotes a hydrophilic group generated by
removal of one hydroxyl group from any one selected from the group
consisting of glycerol, erythritol, pentaerythritol, diglycerol,
triglycerol, xylose, sorbitol, ascorbic acid, glucose, galactose,
mannose, dipentaerythritol, maltose, mannitol, and xylitol.
[0017] This amphipathic compound has preferably viscosity of 11.0
Pas or less as determined at 25.degree. C.
[0018] This amphipathic compound has more preferably viscosity of
4.0 Pas or less as determined at 25.degree. C.
[0019] In one embodiment, preferred examples of the amphipathic
compound include the following compounds: [0020] 1)
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol,
[0021] 2) mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol,
[0022] 3) mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)glycerol,
[0023] 4) mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)diglycerol,
[0024] 5)
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside, [0025]
6) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)pentaerythritol,
[0026] 7) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)glycerol,
[0027] 8) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol,
[0028] 9) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)diglycerol,
[0029] 10) mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)glycerol,
[0030] 11) mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)erythritol,
[0031] 12)
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)pentaerythritol,
[0032] 13) mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)diglycerol,
[0033] 14)
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-xylopyranoside, [0034]
15) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)glycerol, [0035]
16) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)erythritol, [0036]
17) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)pentaerythritol,
[0037] 18) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)diglycerol,
[0038] 19) mono-O-(5,9,13-trimethyltetradec-4-enoyl)glycerol,
[0039] 20) mono-O-(5,9,13-trimethyltetradec-4-enoyl)erythritol,
[0040] 21)
mono-O-(5,9,13-trimethyltetradec-4-enoyl)pentaerythritol, [0041]
22) mono-O-(5,9,13-trimethyltetradec-4-enoyl)diglycerol, [0042] 23)
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-xylopyranoside, [0043] 24)
mono-O-(5,9,13-trimethyltetradec-4-enyl)glycerol, [0044] 25)
mono-O-(5,9,13-trimethyltetradec-4-enyl)erythritol, [0045] 26)
mono-O-(5,9,13-trimethyltetradec-4-enyl)pentaerythritol, [0046] 27)
mono-O-(5,9,13-trimethyltetradec-4-enyl)diglycerol, [0047] 28)
mono-O-(3,7,11-trimethyldodec-2-enoyl)glycerol, [0048] 29)
mono-O-(3,7,11-trimethyldodec-2-enoyl)erythritol, [0049] 30)
mono-O-(3,7,11-trimethyldodec-2-enoyl)pentaerythritol, [0050] 31)
mono-O-(3,7,11-trimethyldodec-2-enoyl)diglycerol, [0051] 32)
1-O-(3,7,11-trimethyldodec-2-enyl)-D-xylopyranoside, [0052] 33)
mono-O-(3,7,11-trimethyldodec-2-enyl)glycerol, [0053] 34)
mono-O-(3,7,11-trimethyldodec-2-enyl)erythritol, [0054] 35)
mono-O-(3,7,11-trimethyldodec-2-enyl)pentaerythritol, and [0055]
36) mono-O-(3,7,11-trimethyldodec-2-enyl)diglycerol.
[0056] In another embodiment, particularly preferable examples of
the amphipathic compound include the following compounds: [0057]
(1) mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol,
[0058] (2) mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol,
[0059] (3) mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)glycerol,
[0060] (4) mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)diglycerol,
[0061] (5)
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)triglycerol, [0062]
(6) mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)sorbitol, [0063]
(7) 1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside,
[0064] (8)
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)pentaerythritol, and
[0065] (9) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol.
[2] A base for an injection formulation, which comprises at least
one type of the compound of [1] above.
[0066] This base is more preferably a base for a depot
formulation.
[3] A depot formulation, which comprises the base for depot
formulations of [2] above.
Effects of the Invention
[0067] The amphipathic compound according to the present invention
exhibits significantly low viscosity. Hence, an injection
formulation having viscosity that enables injection can be easily
prepared by adding a drug to the amphipathic compound according to
the present invention. Also, the amphipathic compound according to
the present invention can retain a drug by forming non-lamellar
liquid crystal in an aqueous solvent. Therefore, the amphipathic
compound according to the present invention is administered in
vivo, so that it forms non-lamellar liquid crystal in a body fluid
so as to be able to retain a drug.
BRIEF DESCRIPTION OF THE DRAWINGS
[0068] FIG. 1 shows a scattering curve showing the results of the
SAXS analysis (small-angle scattering measurement) of a
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol/water
system sample. The scattering curve was plotted against scattering
vector length q=(4.pi./.lamda.)sin(.theta./2), wherein .theta.
denotes scattering angle. The vertical axis indicates relative
intensity compared to the intensity of direct beam attenuated by a
semi-transparent beam stopper having a base index of 1.
[0069] FIG. 2 shows a scattering curve showing the results of SAXS
measurement (small-angle scattering measurement) of a
1-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol/water system
sample. The scattering curve is plotted against scattering vector
length q=(4.pi./.lamda.)sin(.theta./2), wherein .theta. denotes
scattering angle. The vertical axis indicates relative intensity
compared to the intensity of a direct beam attenuated by a
semi-transparent beam stopper having a base index of 1.
EMBODIMENTS FOR CARRYING OUT THE INVENTION
Detailed Description of the Invention
[0070] The present invention is described in detail as follows.
1. Amphipathic Compound
[0071] The amphipathic compound according to the present invention
is a compound having the following general formula (I):
##STR00003##
[0072] In the above formula (I), X and Y each denotes a hydrogen
atom or together denote an oxygen atom, n denotes an integer from 0
to 2, m denotes the integer 1 or 2, or R denotes a hydrophilic
group.
[0073] The hydrophilic group R is preferably, but not limited to, a
residue that is generated by removal of one hydroxyl group from any
one selected from the group consisting of glycerol, erythritol,
pentaerythritol, diglycerol, triglycerol, xylose, xylitol,
mannitol, sorbitol, ascorbic acid, glucose, galactose, mannose,
dipentaerythritol, and maltose.
[0074] In addition, the designation in the above formula:
means that the amphipathic compound according to the present
invention is an E-(cis-) or Z-(trans-) geometric isomer, or a
mixture thereof.
[0075] The amphipathic compound names with prefix "mono" as used
herein are, if two or more positional isomers are present,
generally mean each of corresponding positional isomers and a
mixture thereof. For example, when hydrophilic group R above is a
glycerol, an erythritol, or a diglycerol residue, the corresponding
amphipathic compound names with prefix "mono" according to the
present invention generally mean a 1-ester, a 2-ester, and a
mixture thereof; or a 1-ether, a 2-ether, and a mixture thereof.
Specific examples thereof are compounds (2) and (5) described later
and their meanings are as explained concerning positional isomers.
Similarly, when hydrophilic group R is a xylitol, a mannitol, or a
sorbitol residue, the corresponding amphipathic compound names with
prefix "mono" according to the present invention generally mean 1-
to 3-esters and a mixture of two or more of these esters; or 1- to
3-ethers and a mixture of two or more of these ethers. When
hydrophilic group R is an ascorbic acid residue, the corresponding
amphipathic compound names with prefix "mono" according to the
present invention generally mean 2-, 3-, 5-, and 6-esters and a
mixture of two or more of these esters; or 2-, 3-, 5-, and 6-ethers
and a mixture of two or more of these ethers.
[0076] In the above formula of the amphipathic compound of the
present invention, "n" may be an integer from 0 to 2, and n=0 or 2
is more preferable, and n=2 is even more preferable. Similarly, in
the above formula, "m" may be the integer 1 or 2, and m=2 is more
preferable.
[0077] In the amphipathic compound of the present invention, a
hydrophobic hydrocarbon chain may have a carbon number of C15, C16,
or C17 (wherein m=1, n=0, 1, or 2) or C20, C21, or C22 (wherein
m=2, n=0, 1, or 2).
[0078] One embodiment of the amphipathic compound of the present
invention is preferably a compound defined with and m=2 in the
above formula. Specifically, such compound is one having the above
formula in which the hydrophilic group R is bound to the
hydrophobic hydrocarbon chain being
5,9,13,17-tetramethyloctadec-4-enoyl or
5,9,13,17-tetramethyloctadec-4-enyl, via ester bond or ether bond,
respectively. Specific examples of the compound include the
following compounds. [0079] (1)
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol [0080]
(2) mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol
[0081] Herein,
"mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol" includes
two positional isomers,
1-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol (that is,
1-ester) and 2-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol
(that is, 2-ester), and a mixture thereof [0082] (3)
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside [0083]
(4) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)pentaerythritol
[0084] (5)
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
[0085] Herein,
"mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol" includes
two positional isomers,
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol (that is,
1-ether) and 2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
(that is, 2-ether), and a mixture thereof. [0086] (6)
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)glycerol [0087] (7)
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)diglycerol [0088] (8)
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)triglycerol [0089] (9)
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)xylitol [0090] (10)
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)mannitol [0091] (11)
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)sorbitol [0092] (12)
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)ascorbic acid [0093]
(13) mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)dipentaerythritol
[0094] (14) 1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-glucoside
[0095] (15) 1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-galactoside
[0096] (16) 1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-mannoside
[0097] (17) 1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-maltoside
[0098] (18) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)glycerol
[0099] (19) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)diglycerol
[0100] (20) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)triglycerol
[0101] (21) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)xylitol
[0102] (22) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)mannitol
[0103] (23) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)sorbitol
[0104] (24) mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)ascorbic
acid [0105] (25)
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)dipentaerythritol
[0106] Herein, the meaning of the designation "mono" for the above
compounds (6) to (12) and (18) to (24) is as described above.
[0107] Another preferred embodiment of the amphipathic compound of
the present invention is a compound having the above formula
wherein n=0 and m=2. The hydrophobic hydrocarbon chain of the
compound may be from phytol. Specifically, the compound is one
having the above formula in which the hydrophilic group R is bound
to the hydrophobic hydrocarbon chain being
3,7,11,15-tetramethylhexadec-2-enoyl or
3,7,11,15-tetramethylhexadec-2-enyl, via ester bond or ether bond,
respectively. Specific examples of the compound include the
following compounds. [0108] (26)
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)glycerol [0109] (27)
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)erythritol [0110] (28)
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)pentaerythritol [0111]
(29) mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)diglycerol [0112]
(30) mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)triglycerol
[0113] (31) mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)xylitol
[0114] (32) mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)mannitol
[0115] (33) mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)sorbitol
[0116] (34) mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)ascorbic
acid [0117] (35)
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)dipentaerythritol
[0118] (36)
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-xylopyranoside [0119]
(37) 1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-glucoside [0120]
(38) 1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-galactoside [0121]
(39) 1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-mannoside [0122]
(40) 1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-maltoside [0123]
(41) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)glycerol [0124]
(42) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)erythritol [0125]
(43) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)pentaerythritol
[0126] (44) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)diglycerol
[0127] (45) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)triglycerol
[0128] (46) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)xylitol
[0129] (47) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)mannitol
[0130] (48) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)sorbitol
[0131] (49) mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)ascorbic
acid [0132] (50)
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)dipentaerythritol
[0133] Herein, the meaning of the designation "mono" for the above
compounds (26), (27), (29) to (34), (41), (42), and (44) to (49) is
as described above.
[0134] Another preferred embodiment of the amphipathic compound of
the present invention is a compound having the above formula
wherein n=2 and m=1. The hydrophobic hydrocarbon chain of the
compound can be synthesized using geranylacetone as a starting
material. Specifically, the compound is one having the above
formula in which the hydrophilic group R is bound to the
hydrophobic hydrocarbon chain being
5,9,13-trimethyltetradec-4-enoyl or
5,9,13-trimethyltetradec-4-enyl, via ester bond or ether bond,
respectively. Specific examples of the compound include the
following compounds. [0135] (51)
mono-O-(5,9,13-trimethyltetradec-4-enoyl)glycerol [0136] (52)
mono-O-(5,9,13-trimethyltetradec-4-enoyl)erythritol [0137] (53)
mono-O-(5,9,13-trimethyltetradec-4-enoyl)pentaerythritol [0138]
(54) mono-O-(5,9,13-trimethyltetradec-4-enoyl)diglycerol [0139]
(55) mono-O-(5,9,13-trimethyltetradec-4-enoyl)triglycerol [0140]
(56) mono-O-(5,9,13-trimethyltetradec-4-enoyl)xylitol [0141] (57)
mono-O-(5,9,13-trimethyltetradec-4-enoyl)mannitol [0142] (58)
mono-O-(5,9,13-trimethyltetradec-4-enoyl)sorbitol [0143] (59)
mono-O-(5,9,13-trimethyltetradec-4-enoyl)ascorbic acid [0144] (60)
mono-O-(5,9,13-trimethyltetradec-4-enoyl)dipentaerythritol [0145]
(61) 1-O-(5,9,13-trimethyltetradec-4-enyl)-D-xylopyranoside [0146]
(62) 1-O-(5,9,13-trimethyltetradec-4-enyl)-D-glucoside [0147] (63)
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-galactoside [0148] (64)
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-mannoside [0149] (65)
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-maltoside [0150] (66)
mono-O-(5,9,13-trimethyltetradec-4-enyl)glycerol [0151] (67)
mono-O-(5,9,13-trimethyltetradec-4-enyl)erythritol [0152] (68)
mono-O-(5,9,13-trimethyltetradec-4-enyl)pentaerythritol [0153] (69)
mono-O-(5,9,13-trimethyltetradec-4-enyl)diglycerol [0154] (70)
mono-O-(5,9,13-trimethyltetradec-4-enyl)triglycerol [0155] (71)
mono-O-(5,9,13-trimethyltetradec-4-enyl)xylitol [0156] (72)
mono-O-(5,9,13-trimethyltetradec-4-enyl)mannitol [0157] (73)
mono-O-(5,9,13-trimethyltetradec-4-enyl)sorbitol [0158] (74)
mono-O-(5,9,13-trimethyltetradec-4-enyl)ascorbic acid [0159] (75)
mono-O-(5,9,13-trimethyltetradec-4-enyl)dipentaerythritol
[0160] Herein, the meaning of the designation "mono" for the above
compounds (51), (52), (54) to (59), (66), (67), and (69) to (74) is
as described above.
[0161] Another preferred embodiment of the amphipathic compound of
the present invention is a compound having the above formula
wherein n=0 and m=1. The hydrophobic hydrocarbon chain of the
compound may be from tetrahydro farnesol. Specifically, the
compound is one having the above formula in which the hydrophilic
group R is bound to the hydrophobic hydrocarbon chain being
3,7,11-trimethyldodec-2-enoyl or 3,7,11-trimethyldodec-2-enyl, via
ester bond or ether bond, respectively. Specific examples of the
compound include the following compounds. [0162] (76)
mono-O-(3,7,11-trimethyldodec-2-enoyl)glycerol [0163] (77)
mono-O-(3,7,11-trimethyldodec-2-enoyl)erythritol [0164] (78)
mono-O-(3,7,11-trimethyldodec-2-enoyl)pentaerythritol [0165] (79)
mono-O-(3,7,11-trimethyldodec-2-enoyl)diglycerol [0166] (80)
mono-O-(3,7,11-trimethyldodec-2-enoyl)triglycerol [0167] (81)
mono-O-(3,7,11-trimethyldodec-2-enoyl)xylitol [0168] (82)
mono-O-(3,7,11-trimethyldodec-2-enoyl)mannitol [0169] (83)
mono-O-(3,7,11-trimethyldodec-2-enoyl)sorbitol [0170] (84)
mono-O-(3,7,11-trimethyldodec-2-enoyl)ascorbic acid [0171] (85)
mono-O-(3,7,11-trimethyldodec-2-enoyl)dipentaerythritol [0172] (86)
1-O-(3,7,11-trimethyldodec-2-enyl)-D-xylopyranoside [0173] (87)
1-O-(3,7,11-trimethyldodec-2-enyl)-D-glucoside [0174] (88)
1-O-(3,7,11-trimethyldodec-2-enyl)-D-galactoside [0175] (89)
1-O-(3,7,11-trimethyldodec-2-enyl)-D-mannoside [0176] (90)
1-O-(3,7,11-trimethyldodec-2-enyl)-D-maltoside [0177] (91)
mono-O-(3,7,11-trimethyldodec-2-enyl)glycerol [0178] (92)
mono-O-(3,7,11-trimethyldodec-2-enyl)erythritol [0179] (93)
mono-O-(3,7,11-trimethyldodec-2-enyl)pentaerythritol [0180] (94)
mono-O-(3,7,11-trimethyldodec-2-enyl)diglycerol [0181] (95)
mono-O-(3,7,11-trimethyldodec-2-enyl)triglycerol [0182] (96)
mono-O-(3,7,11-trimethyldodec-2-enyl)xylitol [0183] (97)
mono-O-(3,7,11-trimethyldodec-2-enyl)mannitol [0184] (98)
mono-O-(3,7,11-trimethyldodec-2-enyl)sorbitol [0185] (99)
mono-O-(3,7,11-trimethyldodec-2-enyl)ascorbic acid [0186] (100)
mono-O-(3,7,11-trimethyldodec-2-enyl)dipentaerythritol
[0187] Herein, the meaning of the designation "mono" for the above
compounds (76), (77), (79) to (84), (91), (92), and (94) to (99) is
as described above.
[0188] Another preferred embodiment of the amphipathic compound of
the present invention is a compound having the above formula
wherein n=1 and m=2. The hydrophobic hydrocarbon chain of the
compound may be from phytol. Specifically, the compound is one
having the above formula in which the hydrophilic group R is bound
to the hydrophobic hydrocarbon chain being
4,8,12,16-tetramethylheptadec-3-enoyl or
4,8,12,16-tetramethylheptadec-3-enyl, via ester bond or ether bond,
respectively. Specific examples of the compound include the
following compounds. [0189] (101)
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)glycerol [0190] (102)
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)erythritol [0191]
(103) mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)pentaerythritol
[0192] (104)
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)diglycerol [0193]
(105) mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)triglycerol
[0194] (106) mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)xylitol
[0195] (107) mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)mannitol
[0196] (108) mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)sorbitol
[0197] (109) mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)ascorbic
acid [0198] (110)
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)dipentaerythritol
[0199] (111)
1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-xylopyranoside [0200]
(112) 1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-glucoside [0201]
(113) 1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-galactoside
[0202] (114) 1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-mannoside
[0203] (115) 1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-maltoside
[0204] (116) mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)glycerol
[0205] (117)
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)erythritol [0206]
(118) mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)pentaerythritol
[0207] (119)
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)diglycerol [0208]
(120) mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)triglycerol
[0209] (121) mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)xylitol
[0210] (122) mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)mannitol
[0211] (123) mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)sorbitol
[0212] (124) mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)ascorbic
acid [0213] (125)
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)dipentaerythritol
[0214] Herein, the meaning of the designation "mono" for the above
compounds (101), (102), (104) to (109), (116), (117), and (119) to
(124) is as described above.
[0215] Another preferred embodiment of the amphipathic compound of
the present invention is a compound having the above formula
wherein n=1 and m=1. The hydrophobic hydrocarbon chain of the
compound may be from tetrahydro farnesol. Specifically, the
compound is one having the above formula in which the hydrophilic
group R is bound to the hydrophobic hydrocarbon chain being
4,8,12-trimethyltridec-3-enoyl or 4,8,12-trimethyltridec-3-enyl,
via ester bond or ether bond, respectively. Specific examples of
the compound include the following compounds. [0216] (126)
mono-O-(4,8,12-trimethyltridec-3-enoyl)glycerol [0217] (127)
mono-O-(4,8,12-trimethyltridec-3-enoyl)erythritol [0218] (128)
mono-O-(4,8,12-trimethyltridec-3-enoyl)pentaerythritol [0219] (129)
mono-O-(4,8,12-trimethyltridec-3-enoyl)diglycerol [0220] (130)
mono-O-(4,8,12-trimethyltridec-3-enoyl)triglycerol [0221] (131)
mono-O-(4,8,12-trimethyltridec-3-enoyl)xylitol [0222] (132)
mono-O-(4,8,12-trimethyltridec-3-enoyl)mannitol [0223] (133)
mono-O-(4,8,12-trimethyltridec-3-enoyl)sorbitol [0224] (134)
mono-O-(4,8,12-trimethyltridec-3-enoyl)ascorbic acid [0225] (135)
mono-O-(4,8,12-trimethyltridec-3-enoyl)dipentaerythritol [0226]
(136) 1-O-(4,8,12-trimethyltridec-3-enyl)-D-xylopyranoside [0227]
(137) 1-O-(4,8,12-trimethyltridec-3-enyl)-D-glucoside [0228] (138)
1-O-(4,8,12-trimethyltridec-3-enyl)-D-galactoside [0229] (139)
1-O-(4,8,12-trimethyltridec-3-enyl)-D-mannoside [0230] (140)
1-O-(4,8,12-trimethyltridec-3-enyl)-D-maltoside [0231] (141)
mono-O-(4,8,12-trimethyltridec-3-enyl)glycerol [0232] (142)
mono-O-(4,8,12-trimethyltridec-3-enyl)erythritol [0233] (143)
mono-O-(4,8,12-trimethyltridec-3-enyl)pentaerythritol [0234] (144)
mono-O-(4,8,12-trimethyltridec-3-enyl)diglycerol [0235] (145)
mono-O-(4,8,12-trimethyltridec-3-enyl)triglycerol [0236] (146)
mono-O-(4,8,12-trimethyltridec-3-enyl)xylitol [0237] (147)
mono-O-(4,8,12-trimethyltridec-3-enyl)mannitol [0238] (148)
mono-O-(4,8,12-trimethyltridec-3-enyl)sorbitol [0239] (149)
mono-O-(4,8,12-trimethyltridec-3-enyl)ascorbic acid [0240] (150)
mono-O-(4,8,12-trimethyltridec-3-enyl)dipentaerythritol
[0241] Herein, the meaning of the designation "mono" for the above
compounds (126), (127), (129) to (134), (141), (142), and (144) to
(149) is as described above.
[0242] The amphipathic compound according to the present invention
is more generally an ether or ester compound, wherein one molecule
of long chain unsaturated hydrocarbon, preferably, long chain
unsaturated fatty acid or long chain unsaturated alcohol, is bound
via an ether bond or an ester bond to one molecule of polyhydric
alcohol (preferably, glycerol, erythritol, pentaerythritol,
diglycerol, triglycerol, xylose, sorbitol, ascorbic acid, glucose,
galactose, mannose, dipentaerythritol, or maltose).
[0243] The amphipathic compound according to the present invention
can be synthesized in reference to the Examples described later.
More generally, the amphipathic compound according to the present
invention can be produced as described below, for example.
[0244] First, among compounds having the above general formula (I),
an ester compound (the compound having the following general
formula (I-1)) wherein X and Y together denote an oxygen atom can
be produced by transesterification reaction between an ester
compound having the following general formula (II) and a
hydrophilic compound R--OH, for example. Reaction conditions for
transesterification are not particularly limited, and
transesterification is carried out using an acid or base catalyst,
for example.
##STR00004##
[0245] Furthermore, an ester compound (the compound having general
formula (I-1)) can be produced by esterification between carboxylic
acid corresponding to an ester compound having general formula (II)
and a hydrophilic compound R--OH. Reaction conditions for
esterification are not particularly limited and, for example,
esterification is carried out using an acid or base catalyst or a
condensing agent.
[0246] Some or all hydroxyl groups within R of a hydrophilic
compound R--OH may be protected during transesterification or
esterification reaction. In this case, an ester compound (I-1) can
be produced by transesterification or esterification reaction
followed by deprotection.
[0247] Second, among compounds having the above general formula
(I), an ether compound (the compound having the following general
formula (I-2)) wherein X and Y are both hydrogen atoms can be
produced by etherification reaction between a compound having the
following general formula (III) that has a leaving group Z and a
hydrophilic compound R--OH, or by etherification reaction between
an alcohol having the following general formula (IV) and a compound
R--Z having a leaving group Z, for example. Reaction conditions for
etherification are not particularly limited, and, for example,
etherification is carried out using a base. Etherification reaction
may also be carried out with protecting some or all hydroxyl groups
within R of hydrophilic compound R--OH. In this case, the ether
compound (I-2) can be produced by etherification reaction followed
by deprotection.
##STR00005##
[0248] Third, among compounds having the above general formula (I),
a glycoside compound having general formula (I-2), wherein X and Y
are both hydrogen atoms and R is a sugar residue, can be produced
by glycosylation reaction of an alcohol having general formula (IV)
with saccharides R''--Z having a protected hydroxyl group and a
leaving group Z at the anomeric position, followed by deprotection
(R''.fwdarw.R). Reaction conditions for glycosylation are not
particularly limited, and, for example, glycosylation is carried
out using Lewis acids. Reaction conditions for deprotection are
also not particularly limited, and, for example, deprotection is
carried out by using elimination reaction conditions selected so
that a glycosidic linkage is not impaired at a specific protecting
group.
##STR00006##
[0249] Compounds having the above general formulae (II), (III), and
(IV) can be synthesized as described below, but, the synthesis
method is not limited thereto.
[0250] An ester compound having the formula (II) wherein n=2 and
m=2 can be obtained via Johnson-Claisen reaction using orthoacetate
from isophytol, for example.
[0251] An ester compound having the above formula (II) wherein n=2
and m=1 can be obtained by Johnson-Claisen reaction using
orthoacetate from 3,7,11-trimethyldodec-1-en-3-ol
(tetrahydronerolidol), for example.
[0252] An ester compound having the formula (II) wherein n=1 and
m=2 can be obtained by brominating the hydroxyl group of phytols
and then causing a Grignard reagent generated by adding metal
magnesium to react with carbon dioxide or carrying out substitution
reaction with cyanide followed by hydrolysis to produce carboxylic
acids, and then further carrying out esterification, for
example.
[0253] An ester compound having the formula (II) wherein n=1 and
m=1 can be obtained by brominating the hydroxyl group of
3,7,11-trimethyldodec-2-en-1-ol (tetrahydro farnesol) and then
causing a Grignard reagent generated by adding metal magnesium to
react with carbon dioxide or carrying out substitution reaction
with cyanide followed by hydrolysis to produce carboxylic acids,
and then further carrying out esterification, for example.
[0254] An ester compound having the formula (II) wherein n=0 and
m=2 can be obtained by oxidizing phytols to produce carboxylic
acids and then further carrying out esterification, for
example.
[0255] An ester compound having the formula (II) wherein n=0 and
m=1 can be obtained by oxidizing 3,7,11-trimethyldodec-2-en-1-ol
(tetrahydro farnesol) to produce carboxylic acids and then further
carrying out esterification, for example.
[0256] An alcohol having the formula (IV) wherein n=2 and m=2 can
be obtained by reducing ester compounds having the formula (II)
wherein n=2 and m=2 or the corresponding carboxylic acid using
lithium aluminum hydride or the like. The alcohol having the
formula (IV) wherein n=2 and m=1; n=1 and m=2; or n=1 and m=1 can
be similarly obtained by reducing the ester compound having the
formula (II) wherein n=2 and m=1; n=1 and m=2; or n=1 and m=1,
respectively, or its corresponding carboxylic acid using lithium
aluminum hydride or the like.
[0257] The alcohol having the formula (IV) wherein n=0 and m=2 is a
phytol and is commercially available. However, the alcohol can also
be obtained by reducing the ester compound having the formula (II)
wherein n=0 and m=2 or its corresponding carboxylic acid using
lithium aluminum hydride or the like, for example.
[0258] The alcohol having the formula (IV) wherein n=0 and m=1 is
3,7,11-trimethyldodec-2-en-1-ol (tetrahydro farnesol), and the
compound can be obtained by reducing the ester compound having the
formula (II) wherein n=0 and m=1 or its corresponding carboxylic
acid using lithium aluminum hydride or the like, for example.
[0259] The compound having the formula (III) with the leaving group
Z wherein n=2 and m=2 can be obtained by converting the alcohol
having the formula (IV) wherein n=2 and m=2 to sulfonyloxy group
(e.g., tosyl group or mesyl group) or a leaving group such as a
halogen atom (e.g., a bromine atom or an iodine atom). The compound
having the formula (III) with the leaving group Z wherein n=2, and
m=1; n=1 and m=2; n=0 and m=2; or n=0 and m=1 can be similarly
obtained by converting the alcohol having the formula (IV) wherein
n=2 and m=1; n=1 and m=2; n=0 and m=2; or n=0 and m=1,
respectively, to a leaving group.
[0260] The amphipathic compound according to the present invention
may be any one of the above compounds (1) to (150) prepared by
further substituting a hydrogen atom or a hydroxyl group with any
substituent.
[0261] It is preferably verified that the thus synthesized
compounds are compounds of interest, by using conventional methods
such as infrared spectroscopy measurement or NMR measurement.
2. Viscosity of Amphipathic Compound
[0262] The amphipathic compound according to the present invention
is in a liquid or a semi-solid state with low viscosity within
relatively a wide temperature range. The amphipathic compound
according to the present invention preferably has viscosity of 11
Pas or less, generally 10 Pas or less, more preferably 4.0 Pas or
less (e.g., 3.5 Pa-s or less), and further preferably 2.0 Pas or
less, as measured using a viscometer at 25.degree. C., for example.
Such measured viscosity is typically measured at a shear rate of
105.7 l/s. To obtain such a measured value, an AR Rheometer (AR-G2,
TA Instrument) or a viscosity and viscoelasticity measuring
apparatus MARS (Thermo Fisher Scientific K.K.) can be used as a
viscometer.
[0263] The amphipathic compound according to the present invention
has low viscosity that allows it to pass through a 22 gauge
injection needle (internal diameter: 0.41 mm) or an injection
needle having a width of a lower value than the diameter, more
preferably a 26 gauge injection needle (internal diameter: 0.26 mm)
or an injection needle having a width of a lower value than the
diameter, further preferably a 30 gauge injection needle (internal
diameter: 0.15 mm) or an injection needle having a width of a lower
value than the diameter, and particularly preferably a very thin 31
gauge injection needle (internal diameter: 0.13 mm).
3. Liquid Crystal Forming Capacity of Amphipathic Compound
[0264] The amphipathic compound according to the present invention
is a liquid crystal compound capable of forming non-lamellar liquid
crystal in an aqueous medium. In this Description, an aqueous
medium containing an amphipathic compound may be referred to as an
"amphipathic compound/water system."
[0265] Non-lamellar liquid crystal formed by the amphipathic
compound according to the present invention is preferably type II
(water-in-oil) liquid crystal wherein hydrophobic groups are
oriented outward. Specifically, non-lamellar liquid crystal is more
preferably cubic liquid crystal or reverse hexagonal liquid
crystal.
[0266] Cubic liquid crystal is preferably type II cubic liquid
crystal. Cubic liquid crystal structures are generally classified
into type I and type II. Cubic liquid crystal having an
"oil-in-water" structure is referred to as type I cubic liquid
crystal, and in contrast, cubic liquid crystal having a
"water-in-oil" structure is referred to as type II cubic liquid
crystal. Type I and type II can be determined on the basis of the
phase behavior of an amphipathic compound/water system. For
example, in the case of type I, as the water content of an
amphipathic compound/water system is increased, it is transformed
to another type of liquid crystal (e.g., lamellar liquid crystal)
and then to micells, and it is finally transformed into a uniform
aqueous solution. On the other hand, in the case of the type II
liquid crystal, when its water content reaches a certain level or
higher, it is transformed into a double phase of "liquid
crystal+excess water" in which liquid crystal containing a
saturated volume of water and excess water coexist. Thus, even if
the water content is increased, no uniform aqueous solution is
formed.
[0267] Cubic liquid crystal may also be cubic liquid crystal
belonging to the crystallographic space group Ia3d (hereinafter,
Ia3d cubic liquid crystal), cubic liquid crystal belonging to the
crystallographic space group Pn3m (hereinafter, Pn3m cubic liquid
crystal), or cubic liquid crystal belonging to the crystallographic
space group Im3m (hereinafter, Im3m cubic liquid crystal). Cubic
liquid crystal is more preferably Pn3m cubic liquid crystal.
[0268] Aqueous media in which the amphipathic compound according to
the present invention can form non-lamellar liquid crystal include,
but not limited to, water such as sterile water, purified water,
distilled water, ion exchanged water, and ultrapure water;
electrolyte aqueous solutions such as a physiological saline, an
aqueous sodium chloride solution, an aqueous calcium chloride
solution, an aqueous magnesium chloride solution, an aqueous sodium
sulfate solution, an aqueous potassium sulfate solution, an aqueous
sodium carbonate solution, and an aqueous sodium acetate solution;
buffer solutions such as a phosphate buffer solution and a Tris-HCl
buffer solution; aqueous solutions containing water-soluble organic
substances such as glycerin, ethylene glycol, and ethanol; aqueous
solutions containing sugar molecules such as glucose, sucrose, and
maltose; aqueous solutions containing water soluble polymers, such
as polyethylene glycol and polyvinyl alcohol; aqueous solutions
containing surfactants such as octyl glucoside, dodecyl maltoside,
pluronic (polyethylene glycol/polypropylene glycol/polyethylene
glycol copolymer); and body fluids such as intracellular fluid,
extracellular fluid, intercellular fluid, lymph fluid, spinal
fluid, blood, gastric juice, serum, blood plasma, saliva, tears,
seminal fluid, and urine.
[0269] The amphipathic compound according to the present invention
exhibits high stability under broad environmental conditions. For
example, the amphipathic compound according to the present
invention has high resistance to hydrolysis and high oxidation
stability, although it has a double bond. The amphipathic compound
according to the present invention has also low Krafft temperature,
so that it can stably form liquid crystal even under low
temperatures (6.degree. C. or less, preferably 0.degree. C. or
less).
[0270] The amphipathic compound according to the present invention
can form non-lamellar liquid crystal (preferably cubic liquid
crystal or reverse hexagonal liquid crystal) in an aqueous medium
typically under relatively wide temperature conditions including
room temperature. One or more types of amphipathic compound
according to the present invention can be added to an aqueous
medium at a concentration ranging from 0.1% by mass to 90% by mass,
for example, compared to the total mass of the aqueous medium
containing the amphipathic compound according to the present
invention, preferably, at a concentration forming water-excess
conditions (e.g., 50% by mass to 80% by mass). The solution is then
mixed, preferably uniformly, under temperature conditions ranging
from -10.degree. C. to 80.degree. C., and preferably ranging from
0.degree. C. to 40.degree. C., provided that a subfreezing
temperature is employed under conditions that the aqueous medium
does not freeze, such as supercooled state and under conditions
other than such conditions, temperatures of 0.degree. C. or higher
are employed. As a result, liquid crystal can be stably formed in
the aqueous medium from the amphipathic compound according to the
present invention.
[0271] When the amphipathic compound according to the present
invention is administered in vivo, for example, it can stably form
type II non-lamellar liquid crystal in body fluid, including, but
are not limited to, intracellular fluid, extracellular fluid,
intercellular fluid, lymph fluid, spinal fluid, blood, gastric
juice, serum, blood plasma, saliva, tears, seminal fluid, and
urine.
[0272] When causing liquid crystal to form in an aqueous medium
using the amphipathic compound according to the present invention,
one or more types of amphipathic compound are preferably uniformly
dispersed in the aqueous medium. When causing type II non-lamellar
liquid crystal to form in vitro, an aqueous solvent containing the
amphipathic compound according to the present invention added is
preferably, but not particularly limited to, sufficiently mixed for
1 to 50 hours, for example.
[0273] Herein, an aqueous medium containing the amphipathic
compound according to the present invention, in which liquid
crystal is formed by the amphipathic compound is referred to as a
liquid crystal composition.
[0274] Structural analysis of the thus formed liquid crystal can be
carried out by conventional methods, such as the following
methods.
(1) Observation with Polarizing Microscope
[0275] A penetration method can be used as a method for easily
determining whether or not an amphipathic compound can form liquid
crystal in an aqueous medium or if the amphipathic compound forms
cubic liquid crystal whether or not the thus formed cubic liquid
crystal is of type I or type II. A small amount (several mg) of an
amphipathic compound is placed on microscopic glass slide, and then
pressure is gently applied with a cover glass, so that a thin film
of the amphipathic compound, of which thickness is about 10
microns, is formed (at a diameter ranging from about 1 mm to 5 mm)
in the gap between the glass slide and the cover glass. Water or an
aqueous solvent is added from the side of the gap between the glass
slide and the cover glass via capillary action. Water gradually
penetrates from the outer edge of the amphipathic compound thin
film into the interior, so that a water content gradient is formed
from the amphipathic compound thin film/water interface to the
interior of the amphipathic compound thin film. Polarizing
microscopic observation thereof enables the determination of a
phase type formed depending on the concentration of the amphipathic
compound/water system. Through observation that a region that
imparts the same isotropic texture as that of a water region,
adjacent to the water region (cubic liquid crystals), a region that
imparts bright texture (lamellar liquid crystals), and a region
that imparts isotropic texture (dry amphipathic compounds) are
formed, it is confirmed that the amphipathic compound forms cubic
liquid crystal. Also, it can be determined that the amphipathic
compound is of type II on the basis of the stable formation of
cubic liquid crystal in the interface between the excess water and
the amphipathic compound.
(2) Confirmation of Liquid Crystal Structure by Small Angle X-Ray
Scattering (SAXS) Assay
[0276] Whether or not a liquid crystal structure has a cubic
lattice may be determined by a small-angle X-ray scattering (SAXS)
method, for the purpose of confirming whether or not it is cubic
liquid crystal. First, an amphipathic compound/water system sample
with a predetermined concentration can be added to an X-ray
capillary tube made of quartz, for example, and the capillary tube
is sealed with an oxy-fuel burner, and subjected to SAXS assay.
[0277] Liquid crystal formation can be confirmed by confirming
whether or not the following scattering peak ratio (peak interval)
peculiar to each liquid crystal structure is exhibited as a result
of SAXS measurement
Ratio of Pn3m Cubic Liquid Crystal:
[0278] {square root over (2)}: {square root over (3)}: {square root
over (4)}: {square root over (6)}: {square root over (8)}: {square
root over (9)}: {square root over (10)}: , , , , [Mathematical
expression 1]
Ratio of Ia3d Cubic Liquid Crystal:
[0279] {square root over (3)}: {square root over (4)}: {square root
over (7)}: {square root over (8)}: {square root over (10)}: {square
root over (11)}: , , , , [Mathematical expression 2]
Ratio of Im3m Cubic Liquid Crystal:
[0280] {square root over (2)}: {square root over (4)}: {square root
over (6)}: {square root over (8)}: {square root over (10)}: {square
root over (12)}: {square root over (14)}: , , , , [Mathematical
expression 3]
Ratio Peculiar to Reverse Hexagonal Liquid Crystal:
[0281] 1: {square root over (3)}:2 [Mathematical expression 4]
[0282] A peak value is calculated from SAXS data and then the
reciprocal ratio is found therefrom according to a method known by
persons skilled in the art, so that the space group and the lattice
constant can be easily determined.
4. Use of Amphipathic Compound
[0283] The amphipathic compound according to the present invention
forms type II (water-in-oil) non-lamellar liquid crystal in an
aqueous medium. Upon the liquid crystal formation, the amphipathic
compound according to the present invention enables other
substances (e.g., a drug) in the aqueous medium to be incorporated
and stably retained within the liquid crystal.
[0284] The amphipathic compound that forms type II (water-in-oil)
non-lamellar liquid crystal in an aqueous medium can gradually
release substances incorporated and retained within the liquid
crystal. Therefore, the amphipathic compound according to the
present invention can be used as a base for sustained release
formulations (slow-release formulations).
[0285] Type II non-lamellar liquid crystal that is formed by the
amphipathic compound according to the present invention in an
aqueous medium has strong bioadhesive properties because of the
outward orientation of the hydrophobic groups. The type H
non-lamellar liquid crystal further exhibits a high degree of drug
encapsulation efficiency, can accelerate transdermal absorption of
a drug, and can also accelerate the fine particle dispersion of a
hardly-soluble compound. Therefore, the amphipathic compound
according to the present invention can be broadly and
advantageously used as a base for various formulations. Examples of
such a formulation include, but are not limited to, any
pharmaceutical drugs, quasi drugs, or cosmetics applicable to
living organisms. Examples of a formulation that may be produced
using the amphipathic compound according to the present invention
as a base, include, but are not limited to, liquid formulations or
various similar dosage forms thereto, such as injection
formulations (e.g., a depot formulation, a subcutaneous injection
formulation, an intradermal injection formulation, an intramuscular
injection formulation, an intravenous injection formulation, an
intravenous drip infusion formulation, and an arterial injection
formulation), suppositories, gels, creams (e.g., paste), and oral
formulations (e.g., liquids, an emulsions, and syrups). Of these
examples, parenteral formulations are more preferable dosage forms.
The amphipathic compound according to the present invention can be
added with an active ingredient (typically, a drug) to an aqueous
medium, and then dispersed in the aqueous medium by stirring or the
like, to form an emulsion. This enables the preparation of
formulations retaining the active ingredient and having high
biocompatibility. Alternatively, a formulation may also be prepared
by adding an active ingredient (typically, a drug) to the
amphipathic compound according to the present invention and mixing
them. When the latter formulation is prepared, a pharmaceutically
applicable surfactant may also be added together with an active
ingredient to and dispersed in the amphipathic compound according
to the present invention. In the present invention, the term "base"
in the context of the formulation refers to an ingredient being a
constituent of a formulation (e.g., a carrier, an excipient, a
diluent, or an inactive additive) other than an active ingredient
such as drugs in the case of pharmaceutical drugs or quasi
drugs).
[0286] The amphipathic compound according to the present invention
is a liquid product or a semi-solid product exhibiting
significantly low viscosity such that it can pass through a very
thin injection needle as described above. Therefore, a formulation
prepared by adding and dispersing an active ingredient (typically,
a drug) to and in the amphipathic compound according to the present
invention can also be used as an injection formulation.
Accordingly, the amphipathic compound according to the present
invention can be used particularly advantageously as an ingredient
of a base for an injection formulation. Hence, the present
invention also provides a base for injection formulations
containing the amphipathic compound according to the present
invention.
[0287] An active ingredient (e.g., a drug) to be added to a base
for injection formulations is not particularly limited depending on
the specific properties of the active ingredient including
hydrophilicity or hydrophobicity and molecular sizes (e.g., large
or small), for example. Examples of such an active ingredient,
preferably a drug, include, but are not limited to, a peptide, a
protein, and a low-molecular-weight drug.
[0288] When administered in a living body (in viva), the
amphipathic compound according to the present invention stably
forms type II (water-in-oil) non-lamellar liquid crystal in body
fluid (aqueous medium), incorporates an active ingredient (e.g., a
drug that has been administered together) into the liquid crystal,
stably retains the active ingredient therein, and can further
gradually release it effectively. Thus, the amphipathic compound
according to the present invention can be very advantageously used
for injection formulations possessing sustained drug release
property, and particularly among them, depot formulations.
Therefore, the present invention further provides a base for depot
formulations containing the amphipathic compound according to the
present invention.
[0289] The formulation base and preferably a base for injection
formulations according to the present invention, such as a base for
depot formulations, comprise at least one (one or more) amphipathic
compound according to the present invention. The base for injection
formulations according to the present invention may further contain
one or more carriers, excipients, or inactive additives (e.g.,
preservatives, colorant, and aroma chemicals). The base for
injection formulation according to the present invention may
comprise an aqueous medium. Any aqueous medium that can be used for
bases for injection formulation according to the present invention
can be used. Examples of such an aqueous medium include: water such
as sterile water, purified water, distilled water, ion exchanged
water, and ultrapure water; aqueous electrolyte solutions such as a
physiological saline solution, an aqueous sodium chloride solution,
an aqueous calcium chloride solution, an aqueous magnesium chloride
solution, an aqueous sodium sulfate solution, an aqueous potassium
sulfate solution, an aqueous sodium carbonate solution, and an
aqueous sodium acetate solution; buffer solutions such as a
phosphate buffer solution and a Tris-HCl buffer solution; aqueous
solutions containing water soluble organic substances such as
glycerin, ethylene glycol, and ethanol; aqueous solutions
containing sugar molecules such as glucose, sucrose, and maltose;
aqueous solutions containing water soluble polymers such as
polyethylene glycol and polyvinyl alcohol; and aqueous solutions
containing surfactants such as octyl glucoside, dodecyl maltoside,
and pluronic (polyethylene glycol/polypropylene glycol/polyethylene
glycol copolymer). However, the base for depot formulations
according to the present invention preferably contains no aqueous
medium in view of realization of local administration to a specific
site. Similarly, the depot formulation according to the present
invention preferably contains no aqueous medium. The depot
formulation according to the present invention may be preferably a
mixture of the amphipathic compound according to the present
invention and an active ingredient (e.g., a drug). The depot
formulation according to the present invention may further contain
a pharmaceutically applicable surfactant, as necessary.
[0290] A depot formulation is used for a depot technique, which
involves injecting a base with a drug encapsulated therein in vivo
and then causing sustained drug release therefrom. A depot
formulation prepared by dispersing an active ingredient (typically,
a drug) and, further, a pharmaceutically applicable surfactant as
necessary in the amphipathic compound according to the present
invention has very low viscosity. Hence, such depot formulation can
be administered in vivo using a thin injection needle (via e.g.,
intradermal, subcutaneous or mucous administration). Through
administration of the depot formulation, type II (water-in-oil)
non-lamellar liquid crystal can be stably formed in body fluid at
the administration site. Furthermore, in that case, an active
ingredient contained in the depot formulation and thus
co-administered is incorporated into the liquid crystal and
retained therein, so that it can be gradually released effectively.
The depot formulation prepared using the base for injection
formulations according to the present invention possesses sustained
release property, so that the drug effect can be sustained for a
long time period in a single dose and thus the frequency of drug
administration can be decreased. Also, the depot formulation can be
administered locally to a target site, so that adverse reaction at
sites other than the target site can be minimized. Furthermore, the
depot formulation comprising the amphipathic compound according to
the present invention as a base can be administered using a very
thin injection needle, such as a 30 gauge or a 31 gauge injection
needle, so that the pain caused by injection can be suppressed to a
very low level. With the use of the depot formulation according to
the present invention, an active ingredient (e.g., a drug) can be
encapsulated and retained within liquid crystal at a higher
concentration in vivo and therefore the injection dose to be
administered can be decreased. In this way, the depot formulation
according to the present invention is very useful for improving
patients' QOL (Quality of Life). The present invention further
provides the depot formulation comprising the base for injection
formulations according to the present invention.
[0291] An active ingredient (e.g., a drug) to be contained in the
depot formulation is not particularly limited depending on the
specific properties of the active ingredient, such as
hydrophilicity or hydrophobicity, or by molecular size (large or
small), for example. Examples of such an active ingredient, and
preferably a drug, include, but are not limited to, a peptide, a
protein, and a low-molecular-weight drugs.
[0292] This description includes part or all of the content
disclosed in the description and/or drawings of Japanese Patent
Application No. 2009-295658, which is a priority document of the
present application.
[0293] All publications, patents, and patent applications cited
herein are incorporated herein by reference in their entirety.
EXAMPLES
[0294] The present invention will be explained more specifically
with reference to the following Examples. However, the technical
scope of the present invention is not limited to these
Examples.
[0295] The viscosity of each of the compounds shown in the Examples
1-11 was measured using AR Rheometer (AR-G2, TA Instrument) after
allowing to stand at the temperature of 25.degree. C. for 12
hours.
[0296] Each of the above compounds was confirmed to be capable of
passing through a needle of up to 31 gauge by using syringes
(hypodermic needle; purchased from ASONE Corporation) attached to a
30 gauge needle (bore diameter 0.15 mm) or 31 gauge needle (bore
diameter 0.13 mm).
Example 1
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol
##STR00007##
[0298] Under reduced pressure of 60-70 mmHg and nitrogen gas
stream, 250 g (0.71 mol) of methyl
5,9,13,17-tetramethyloctadec-4-enoate was slowly added dropwise at
78-83.degree. C. to a solution of 157 g (1.15 mol) of
pentaerythritol and 1.58 g (1.15 mmol) of potassium carbonate in
dry N,N-dimethylformamide (700 mL). After the reaction mixture was
stirred at the same temperature for 10 hours, formic acid was added
at 75.degree. C. to adjust the pH to 4. After the resulting
solution was subjected to vacuum concentration, the residue was
diluted with t-butylmethylether (1.5 L), and the resulting
insoluble matter was separated by filtration. The filtrate was
washed with 10% sodium bicarbonate aqueous solution twice, and
decolorized with activated carbon (8 g). After filtration, the
filtrate was concentrated, and the residue was purified by silica
gel column chromatography (hexane/ethyl acetate mixture) to obtain
the title compound.
[0299] Infrared (IR) spectrum by infrared spectroscopy and
viscosity of the obtained compound were measured. The results were
as follows.
[0300] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 12H), 1.00-1.70 (m, 22H), 1.90-2.05 (m, 2H),
2.25-2.45 (m, 4H), 3.64 (s, 6H), 4.24 (s, 2H), 5.07 (brs, 1H).
[0301] IR spectrum (NaCl thin film method): 3387, 2926, 2866, 1739,
1461, 1378, 1267, 1139, 1051.
[0302] Viscosity: 1.7 Pas.
Example 2
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol
[0303] Under reduced pressure of 60-70 mmHg and nitrogen gas
stream, 199 g (0.564 mol) of methyl
5,9,13,17-tetramethyloctadec-4-enoate was slowly added dropwise to
a solution of 191 g (1.56 mol) of erythritol and 1.58 g (1.15 mmol)
of potassium carbonate in dry N,N-dimethylformamide (700 mL) at
78-83.degree. C. After the reaction mixture was stirred at the same
temperature for 10 hours, formic acid was added at 75.degree. C. to
adjust the pH to 4. After the resulting solution was subjected to
vacuum concentration, the residue was diluted with
t-butylmethylether (1.5 L), and the insoluble matter generated was
separated by filtration. The filtrate was washed with 10% sodium
bicarbonate aqueous solution twice, and decolorized with activated
carbon (8 g). After filtration, the filtrate was concentrated, and
the residue was dissolved in ethanol, followed by filtration
through cellulose powder. After the filtrate was concentrated, and
the resulting residue was purified by silica gel column
chromatography (hexane/ethyl acetate mixture) to obtain the title
compound.
[0304] Infrared (IR) spectrum by infrared spectroscopy and
viscosity of the obtained compound were measured. The results were
as follows:
[0305] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 12H), 1.00-1.70 (m, 22H), 1.40-2.05 (m, 2H),
2.25-2.45 (m, 4H), 3.55-3.95 (m, 4H), 4.25-4.40 (m, 2H), 5.09 (dd,
J=4.8 Hz, J=4.8 Hz, 1H).
[0306] IR spectrum (NaCl thin film method): 3407, 2926, 2867, 1738,
1461, 1377, 1269, 1172, 1081.
[0307] Viscosity: 2.0 Pas.
Example 3
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)glycerol
[0308] The title compound was synthesized using the same procedure
as employed in Example 2, but with glycerol instead of erythritol,
having the following properties:
[0309] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 12H), 1.00-1.70 (m, 22H), 1.85-2.15 (m, 2H),
2.15-2.55 (m, 4H), 3.53-3.78 (m, 3H), 3.80-4.00 (m, 1H), 4.10-4.25
(m, 2H), 5.08 (dd, J=6.9 Hz, J=6.9 Hz, 1H).
Example 4
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)diglycerol
[0310] The title compound was synthesized using the same procedure
as employed in Example 2, but with diglycerol instead of
erythritol, having the following properties:
[0311] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 22H), 1.97 (ddd, J=17.4 Hz, J=7.8
Hz, J=6.9 Hz, 2H), 2.20-2.45 (m, 4H), 3.50-4.10 (m, 8H), 4.10-4.25
(m, 2H), 5.08 (dd, J=6.6 Hz, 0.1=6.6 Hz, 1H).
Example 5
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)triglycerol
[0312] The title compound was synthesized using the same procedure
as employed in Example 2, but with triglycerol instead of
erythritol, having the following properties:
[0313] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 22H), 1.97 (ddd, J=17.4 Hz, J=7.8
Hz, 3=7.8 Hz, 2H), 2.25-2.45 (m, 4H), 3.45-4.05 (m, 13H), 4.10-4.20
(m, 2H), 5.08 (brs, 1H).
Example 6
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)sorbitol
[0314] The title compound was synthesized using the same procedure
as employed in Example 2, but with sorbitol instead of erythritol,
having the following properties:
[0315] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 22H), 1.80-2.05 (in, 2H),
2.25-2.45 (m, 4H), 3.50-4.40 (m, 8H), 5.07 (brs, 1H).
Example 7
Synthesis of 5,9,13,17-tetramethyloctadec-4-en-1-ol
##STR00008##
[0317] Under a nitrogen atmosphere, 9.6 g (0.25 mol) of lithium
aluminum hydride was added little by little at 0.degree. C. to a
solution of 150 g (0.425 mol) of methyl
5,9,13,17-tetramethyloctadec-4-enoate in dry tetrahydrofuran (850
mL). After being stirred at 50.degree. C. for 2 hours, the reaction
mixture was cooled on ice, followed by careful addition of water
until the resulting gray suspension turned white. Sodium sulfate
was added to the solution at room temperature for drying. After
filtration, the filtrate was concentrated to obtain 133.8 g of the
title compound (97% yield) as a colorless transparent liquid. The
results of NMR analysis of the resulting compound are as shown
below.
[0318] .sup.1H-NMR spectrum (400 MHz, CDCl.sub.3, TMS) .delta.:
0.7-0.95 (m, 12), 0.95-1.85 (m, 24H), 1.9-2.1 (m, 4H), 3.63 (t,
J=6.5 Hz, 2H), 5.12 (br t, J=7.2 Hz, 1H).
Example 8
Synthesis of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside
triacetate
##STR00009##
[0320] Under a nitrogen atmosphere, 80.0 g (0.251 mol) of
.beta.-xylose tetraacetate and 106 g (0.327 mol) of
5,9,13,17-tetramethyloctadec-4-en-1-ol was dissolved in dry
acetonitrile (0.30 L), and stirred for 30 min. After the solution
was cooled to 0.degree. C., 38 mL (0.30 mol) of boron trifluoride
diethyl etherate complex was added. The reaction mixture was
allowed to warm up to room temperature while being stirred
overnight before addition of 70 mL (0.50 mol) of triethylamine at
0.degree. C. The resulting solution was diluted with ethyl acetate,
and washed with water, 3M hydrochloric acid (twice), saturated
sodium bicarbonate aqueous solution (twice), and saturated brine,
successively, and dried over magnesium sulfate. After filtration,
the filtrate was concentrated to obtain 161.95 g of the title
compound as a crude product. A part of the crude product was
purified by silica gel column chromatography (hexane/ethyl
acetate=85:15). The results of NMR analysis of the resulting
compound are as shown below.
[0321] .sup.1H-NMR spectrum (400 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.95 (m, 12H), 1.0-1.8 (m, 24H), 1.85-2.1 (m, 4H), 2.03 (s,
3H), 2.05 (s, 6H), 3.35 (dd, J=9.12 Hz, 1H), 3.45 (m, 1H), 3.80 (m,
1H), 4.11 (dd, J=5, 12 Hz, 1H), 4.47 (d, J=6.8 Hz, 1H), 4.94 (m,
2H), 5.09 (m, 1H), 5.16 (dd, J=8.7, 8.7 Hz, 1H).
Example 9
Synthesis of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside
##STR00010##
[0323] A solution of 13.4 g (0.248 mmol) of sodium methylate in
methanol (250 mL) was added to a solution of 160.33 g of the crude
product 1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside
triacetate synthesized in Example 8 in methanol/tetrahydrofuran
(1:1, 500 mL) at room temperature. After being stirred for 1 hour,
17.7 mL (0.248 mmol) of acetyl chloride was added to the reaction
solution and then the solution was confirmed to be neutralized.
After addition of water, the solution was extracted with ethyl
acetate (twice). The extracts were washed with saturated brine, and
dried over magnesium sulfate. After filtration, the filtrate was
concentrated, and the resulting residue was purified by silica gel
column chromatography (hexane/ethyl acetate=67:33-0:100) to obtain
24.6 g of the title compound (22% yield in 2 steps) as a colorless
transparent semi-solid. The results of NMR analysis of the
resulting compound are as shown below.
[0324] .sup.1H-NMR spectrum (400 MHz, CDCl.sub.3, TMS) .delta.:
0.7-0.9 (m, 12H), 1.0-1.7 (m, 24H), 1.85-2.1 (m, 4H), 3.29 (dd,
J=9, 11.6 Hz, 1H), 3.41 (m, 1H), 3.45-3.8 (m, 5H), 3.83 (m, 1H),
3.98 (dd, J=4.4, 11.6 Hz, 1H), 4.27 (m, 1H), 4.30 (d, J=6.8 Hz,
1H), 5.10 (m, 1H).
Example 10
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)pentaerythritol
##STR00011##
[0326] Under a nitrogen atmosphere, 55 mL (0.39 mol) of
triethylamine, 59.9 g (0.314 mol) of p-toluenesulfonyl chloride,
and 2.5 g (26 mmol) of trimethylamine hydrochloride were added to a
solution of 85.0 g (0.262 mol) of
5,9,13,17-tetramethyloctadec-4-en-1-ol in dry methylene chloride
(0.26 L) at 0.degree. C., sequentially. After being stirred for 1
hour, 9.9 mL (79 mmol) of N,N-dimethyl-1,3-propanediamine was added
to the reaction solution at 0.degree. C. After being stirred for 1
hour, the mixture was diluted with a mixed solvent of hexane/ethyl
acetate. The resulting solution was washed with water, 3M
hydrochloric acid (twice), saturated sodium bicarbonate aqueous
solution, and saturated brine, successively, and dried over
magnesium sulfate. After filtration, the filtrate was concentrated,
and the resulting residue was purified by silica gel column
chromatography (hexane/ethyl acetate=90:10) to obtain 116 g of
(5,9,13,17-tetramethyloctadec-4-enyl)tosylate (93% yield).
[0327] Under a nitrogen atmosphere, 2.08 g (11.8 mmol) of
2,2-dimethyl-1,3-dioxane-5,5-dimethanol was added to a solution of
0.51 g (63%, 14 mmol) of sodium hydride in dry
N,N-dimethylformamide (18 mL) in several portions, with cooling on
ice. After the mixture was stirred for 1 hour at 50.degree. C., a
solution of 2.81 g (5.88 mmol) of the above
(5,9,13,17-tetramethyloctadec-4-enyl)tosylate in dry
N,N-dimethylformamide (9 mL) was added dropwise thereto for 30 min
with additional stirring for 3 hours at the same temperature. After
addition of water at 0.degree. C., the mixture was extracted with
ethyl acetate. The extract was washed with water, saturated sodium
bicarbonate aqueous solution, and saturated brine, successively,
and dried over magnesium sulfate. After filtration, the filtrate
was concentrated, and the resulting residue was purified by silica
gel column chromatography (hexane/ethyl acetate=85:15) to obtain
1.52 g of
2,2-dimethyl-1,3-dioxane-5-(5,9,13,17-tetramethyloctadec-4-enoxy)methyl-5-
-methanol (54% yield).
[0328] 1.52 g (3.15 mmol) of the above product was dissolved in
methanol (50 mL), and 1 mL (1.25 M, 1.25 mmol) of hydrochloric
acid/methanol was added at room temperature. The reaction mixture
was stirred for 12 hours at room temperature, and subjected to
vacuum concentration. The resulting residue was purified by silica
gel column chromatography (chloroform/methanol=95:5) to obtain 1.15
g of the title compound (83% yield) as a colorless transparent
viscous product. The results of NMR analysis and viscosimetry of
the resulting compound are as shown below.
[0329] .sup.1H-NMR spectrum (400 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 12H), 1.0-1.7 (m, 24H), 1.9-2.1 (m, 4H), 2.43 (m, 3H),
3.43 (t, J=6.6 Hz, 2H), 3.47 (s, 2H), 3.73 (dd, J=1.0, 5.8 Hz, 6H),
5.09 (br t, J=7.3 Hz, 1H).
[0330] Viscosity: 1.9 Pas.
Example 11
Synthesis of 1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
(1-ether), and 2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
(2-ether)
##STR00012##
[0332] Under a nitrogen atmosphere, 0.45 g (63%, 12 mmol) of sodium
hydride was added to a solution of 1.92 g (11.9 mmol) of
1,2-O-isopropylideneerythritol in dry N,N-dimethylformamide (30 mL)
in several portions with cooling on ice. After the mixture was
stirred for 20 min at room temperature, a solution of 4.2 g (1.0
mmol) of (5,9,13,17-tetramethyloctadec-4-enyl)tosylate in dry
N,N-dimethylformamide (30 mL) was added with additional stirring
for 3 hours at 50.degree. C. By thin-layer chromatography (TLC)
analysis, the ratio of
1,2-O-isopropylidene-4-O-(5,9,13,17-tetramethyloctadec-4-enyl)er-
ythritol to
1,2-O-isopropylidene-3-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
generated was approximately 1:1. After addition of water at
0.degree. C., the reaction mixture was extracted with ethyl
acetate. The extract was washed with water, saturated sodium
bicarbonate aqueous solution, and saturated brine, successively,
and dried over magnesium sulfate. After filtration, the filtrate
was concentrated, and the resulting residue was purified by silica
gel column chromatography (hexane/ethyl acetate=90:10 to 85:15) to
obtain 1.12 g of
1,2-O-isopropylidene-4-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
(27% yield) and 1.54 g of
1,2-O-isopropylidene-3-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
(37% yield).
[0333] 1.10 g (2.67 mmol) of the above product
1,2-O-isopropylidene-4-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
and 1.50 g (3.63 mmol) of
1,2-O-isopropylidene-3-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
were each dissolved in 15 mL of methanol added, and 51 mg (0.30
mmol) of p-toluenesulfonic acid monohydrate was added thereto at
room temperature. After being stirred for 5 hours at room
temperature, the each reaction mixture was neutralized by addition
of triethylamine. After vacuum concentration, the resulting each
residue was purified by silica gel column chromatography
(chloroform/methanol=98:2) to obtain 0.60 g of the title 1-ether
compound (1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol) (60%
yield) as a colorless transparent semi-solid and 0.80 g of the
title 2-ether compound
(2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol) (60% yield)
as a colorless transparent viscous product, respectively.
(1) 1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
[0334] .sup.1H-NMR spectrum (400 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 12H), 1.0-1.7 (m, 24H), 1.9-2.1 (m, 4H), 2.32 (dd,
J=5.8, 10.1 Hz, 1H), 2.66 (dd, J=2.4, 5.8 Hz, 1H), 2.78 (t, J=5.8
Hz, 1H), 3.49 (t, J=6.5 Hz, 2H), 3.57 (d, J=4.8, 9.7 Hz, 1H), 3.60
(d, J=5.8, 9.7 Hz, 1H), 3.7-3.8 (m, 3H), 3.82 (m, 1H), 5.10 (br t,
J=7 Hz, 1H).
[0335] Viscosity: 2.3 Pas.
(2) 2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
[0336] .sup.1H-NMR spectrum (400 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 12H), 1.0-1.7 (m, 24H), 1.9-2.1 (m, 4H), 2.3-2.4 (m,
2H), 2.77 (m, 1H), 3.39 (dd, J=5, 10 Hz, 1H), 3.51 (m, 1H), 3.60
(m, 1H), 3.65-3.9 (m, 5H), 5.10 (br t, J=7 Hz, 1H).
[0337] Viscosity: 3.2 Pa's.
Example 12
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
[0338] Under a nitrogen atmosphere, 2.19 g (55%, 50.2 mmol) of
sodium hydride was added to a solution of 14.1 g (83.6 mmol) of
1,2-O-isopropylideneerythritol in dry N,N-dimethylformamide (100
mL) in several portions, with cooling on ice. After the mixture was
stirred for 30 min at room temperature, a solution of 20.0 g (41.8
mmol) of (5,9,13,17-tetramethyloctadec-4-enyl)tosylate in dry
N,N-dimethylformamide (20 mL) was added with additional stirring
for 2 hours at 50.degree. C. By thin-layer chromatography (TLC)
analysis, the ratio of
1,2-O-isopropylidene-4-O-(5,9,13,17-tetramethyloctadec-4-enyl)er-
ythritol to
1,2-O-isopropylidene-3-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
generated was approximately 1:1. After addition of saturated
ammonium chloride aqueous solution at 0.degree. C., the reaction
mixture was extracted with a mixed solvent of hexane/ethyl acetate.
The extract was washed with saturated sodium bicarbonate aqueous
solution and saturated brine successively, and then dried over
magnesium sulfate. After filtration, the filtrate was concentrated
to give 20.5 g of a mixture of
1,2-O-isopropylidene-4-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol
and
1,2-O-isopropylidene-3-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythri-
tol.
[0339] 20.5 g of the above mixture was dissolved in tetrahydrofuran
(190 mL), and 3M hydrochloric acid (60 mL) was added thereto at
room temperature. After being stirred at room temperature
overnight, the reaction mixture was extracted with ethyl acetate.
The extract was washed with water, saturated sodium bicarbonate
aqueous solution, and saturated brine, successively, and dried over
magnesium sulfate. After filtration, the filtrate was concentrated,
and the resulting residue was purified by silica gel column
chromatography (hexane/ethyl acetate=50:50 to 0:100) to obtain 10.4
g of the title compound (53% yield in 2 steps) as a colorless
transparent viscous product.
[0340] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 12H), 1.0-1.7 (m, 24H), 1.9-2.1 (m, 4H), 2.75 (m, 15H),
2.96 (m, 0.5H), 3.13 (m, 0.5H), 3.23 (m, 0.5H), 3.38 (m, 0.5H),
3.45-3.7 (m, 3H), 3.7-3.9 (m, 4.5H), 5.11 (m, 1H).
Example 13
Formation of a liquid crystal by
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol and
analysis thereof
[0341] Mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol
and pure water were introduced into a mixing device at the
concentration of 50 wt %
Mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol
(water-excess condition), and incubation thereof was carried out
while performing 100 or more times of mixing operations at room
temperature (25.degree. C.) over the period of 24 hours. Thus, a
homogeneously mixed sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol/wa-
ter system was obtained. This sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol/water
system appeared to be a white turbid gel composition.
[0342] Subsequently, the thus obtained sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol/water
system was confirmed to be a cubic liquid crystal by small-angle
x-ray scattering (SAXS). The sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol/water
system was introduced into a quartz X-ray capillary tube, the tip
of the capillary was sealed using an oxygen burner, and the
capillary tube was subjected to the SAXS analysis. The NANO-Viewer
nano-scale X-ray structure analysis equipment (Rigaku) was used for
SAXS analysis. SAXS analysis was performed by X-ray irradiation at
room temperature (25.degree. C.), 40 kV, 50 mA, wavelength
.lamda.=0.1542 nm (Cu-K.alpha.) for 15 min.
[0343] As a result of SAXS analysis, 5 sharp scattering peaks were
observed at least. The peak value ratio exhibited the following
ratio peculiar to the cubic liquid crystal belonging to the
crystallographic space group Pn3m:
{square root over (2)}: {square root over (3)}: {square root over
(4)}: {square root over (6)}: {square root over (8)}: {square root
over (9)}.
[0344] Thus, the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol/water
system was confirmed to form a cubic liquid crystal that belong to
the crystallographic space group Pn3m (ac (lattice constant)=7.80
nm).
[0345] The result of SAXS analysis of the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)pentaerythritol/water
system is shown in FIG. 1.
Example 14
Formation of a liquid crystal by
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol and
analysis thereof
[0346] mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol
synthesized in Example 2 and water were homogenously mixed in
accordance with the same procedure as in Example 13 to obtain a
sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol/water
system. SAXS analysis of the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol/water
system was performed in the same manner as in Example 13. As a
result, at least 3 sharp scattering peaks were observed. The peak
value ratio exhibited the following ratio peculiar to the reverse
hexagonal liquid crystal:
1: 3:2.
[0347] Thus, the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol/water
system was confirmed to form a reverse hexagonal liquid
crystal.
[0348] The result of SAXS analysis of the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)erythritol/water
system is shown in FIG. 2.
Example 15
Formation of a liquid crystal by
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside and
analysis thereof
[0349] 1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside
and water were homogeneously mixed in accordance with the same
procedure as in Example 13 to obtain a sample of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside/water
system. SAXS analysis of the sample of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside/water
system was performed in the same manner as in Example 13. As a
result, at least 4 sharp scattering peaks were observed. The peak
value ratio exhibited the following ratio peculiar to the cubic
liquid crystal belonging to the crystallographic space group
Pn3m:
{square root over (2)}: {square root over (3)}: {square root over
(4)}: {square root over (6)}: {square root over (8)}: {square root
over (9)}.
[0350] Thus, the sample of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-xylopyranoside/water
system was confirmed to form a cubic liquid crystal that belong to
the crystallographic space group Pn3m (ac=8.9 nm).
Example 16
Formation of a liquid crystal by
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)pentaerythritol and
analysis thereof
[0351] Mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)pentaerythritol
and water were homogeneously mixed in accordance with the same
procedure as in Example 13 to obtain a sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)pentaerythritol/water
system. SAXS analysis of the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)pentaerythritol/water
system was performed in the same manner as in Example 13. As a
result, at least 3 sharp scattering peaks were observed. The peak
value ratio exhibited the following ratio peculiar to the reverse
hexagonal liquid crystal:
1: {square root over (3)}:2.
[0352] Thus, the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)pentaerythritol/water
system was confirmed to form a reverse hexagonal liquid
crystal.
Example 17
Formation of a liquid crystal by
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and analysis
thereof
[0353] 1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and
water were homogeneously mixed in accordance with the same
procedure as in Example 13 to obtain a sample of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol/water system.
SAXS analysis of the sample of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol/water system
was performed in the same manner as in Example 13. As a result, at
least 3 sharp scattering peaks were observed. The peak value ratio
exhibited the following ratio peculiar to the reverse hexagonal
liquid crystal:
1: {square root over (3)}:2.
[0354] Thus, the sample of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol/water system
was confirmed to form a reverse hexagonal liquid crystal.
Example 18
Formation of a liquid crystal by
2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and analysis
thereof
[0355] 2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and
water were homogeneously mixed in accordance with the same
procedure as in Example 13 to obtain a sample of
2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol/water system.
SAXS analysis of the sample of
2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol/water system
was performed in the same manner as in Example 13. As a result, at
least 4 sharp scattering peaks were observed. The peak value ratio
exhibited the following ratio peculiar to the cubic liquid crystal
belonging to the crystallographic space group Pn3m:
{square root over (2)}: {square root over (3)}: {square root over
(4)}: {square root over (6)}: {square root over (8)}: {square root
over (9)}.
[0356] Thus, the sample of
2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol/water system
was confirmed to form a cubic liquid crystal that belong to the
crystallographic space group Pn3m (ac=8.9 nm).
Example 19
Formation of a liquid crystal by a mixture (1:1) of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and
2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and analysis
thereof
[0357] A mixture (1:1) of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and
2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and water were
homogeneously mixed in accordance with the same procedure as in
Example 13 to obtain a sample of the mixture (1:1) of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and
2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol/water system.
SAXS analysis of the sample of the mixture (1:1) of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and
2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol/water system
was performed in the same manner as in Example 13. As a result, at
least 3 sharp scattering peaks were observed. The peak value ratio
exhibited the following ratio peculiar to the reverse hexagonal
liquid crystal:
1: {square root over (3)}:2.
[0358] Thus, the sample of the mixture (1:1) of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol and
2-O-(5,9,13,17-tetramethyloctadec-4-enyl)erythritol/water system
was confirmed to form a reverse hexagonal liquid crystal.
Example 20
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)xylitol
##STR00013##
[0360] 1.0 g (2.8 mmol) of methyl
5,9,13,17-tetramethyloctadec-4-enoate was slowly added dropwise to
a solution of 0.86 g (2.8 mmol) of xylitol and 0.78 g (5.7 mmol) of
potassium carbonate in dry N,N-dimethylformamide (2.5 mL) at
80.degree. C. After the reaction mixture was stirred at 100.degree.
C. for 24 hours, the potassium carbonate was separated by
filtration. The resulting solution was diluted with
t-butylmethylether, and washed with water, 1M hydrochloric acid,
saturated sodium bicarbonate aqueous solution, and saturated brine,
successively, and dried over magnesium sulfate. After filtration,
the filtrate was concentrated, and the resulting residue was
purified by silica gel column chromatography (methanol/methylene
chloride mixture) to obtain 146 mg of the title compound (12%
yield) as a colorless viscous product.
[0361] The results of 1H-NMR analysis of the thus obtained product
are as shown below.
[0362] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 22H), 1.90-2.05 (m, 2H),
2.25-2.45 (m, 4H), 3.65 (brs, 1H), 3.70-3.90 (m, 3H), 4.02 (brs,
1H), 4.24 (d, J=5.9 Hz, 2H), 5.08 (brs, 1H).
Example 21
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)mannitol
##STR00014##
[0364] The title compound was synthesized using the same procedure
as employed in Example 20, but with 1.0 g (5.7 mmol) of mannitol
instead of xylitol. The compound was obtained as a white semi-solid
(21% yield) having the following properties:
[0365] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3+3% CD.sub.3OD,
TMS) .delta.: 0.80-0.95 (m, 12H), 1.00-1.58 (m, 19H), 1.60 and 1.67
(s, 3H, 5-CH.sub.3), 1.90-2.00 (m, 2H), 2.25-2.45 (m, 4H),
3.65-3.95 (m, 6H), 4.26 (dd, J=5.9, 11.3 Hz, 1H), 4.38 (d, J=12.0
Hz, 1H), 5.08 (brs, 1H).
Example 22
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)dipentaerythritol
##STR00015##
[0367] The title compound was synthesized using the same procedure
as employed in Example 20, but with 1.44 g (5.67 mmol) of
dipentaerythritol instead of xylitol. The compound was obtained as
a white powder (13% yield) having the following properties:
[0368] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3+3% CD.sub.3OD,
TMS) .delta.: 0.80-0.90 (m, 12H), 1.00-1.70 (m, 22H), 1.85-2.00 (m,
2H), 2.25-2.40 (m, 4H), 3.36 (s, 4H), 3.53 (brs, 10H), 4.04 (s,
2H), 5.05 (brs, 1H).
Example 23
Synthesis of mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)ascorbic
acid
##STR00016##
[0370] 0.50 g (2.8 mmol) of ascorbic acid was dissolved in
concentrated sulfuric acid (14 mL). After addition of 1.0 g (2.8
mmol) of methyl 5,9,13,17-tetramethyloctadec-4-enoate, the mixture
was stirred for 24 hours at room temperature. The reaction mixture
was poured into iced water, and extracted with ethyl acetate. The
extract was washed with water, 1M hydrochloric acid, saturated
sodium bicarbonate aqueous solution, and saturated brine,
successively, and dried over sodium sulfate. After filtration, the
filtrate was concentrated, and the resulting residue was purified
by silica gel column chromatography (methanol/methylene chloride
mixture) to obtain the title compound.
Example 24
Synthesis of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-glucoside
##STR00017##
[0372] 3.0 g (7.7 mmol) of .beta.-D-Glucose pentaacetate and 324 g
(9.99 mmol) of 5,9,13,17-tetramethyloctadec-4-en-1-ol were
dissolved in dry acetonitrile (8 mL). 1.95 mL (15.4 mmol) of boron
trifluoride diethyl etherate complex was added to the solution with
cooling on ice. The reaction mixture was allowed to warm up slowly
to room temperature while being stirred overnight before addition
of 3.2 mL (23 mmol) of triethylamine at 0.degree. C. The resulting
solution was diluted with ethyl acetate, and washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over sodium sulfate.
After filtration, the filtrate was concentrated to obtain
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-glucopyranoside
tetraacetate as a crude product.
[0373] The above crude product of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-glucopyranoside
tetraacetate was dissolved in methanol/tetrahydrofuran (1:1, 50
mL), and 0.77 mL (0.77 mmol) of 1M sodium methylate in methanol was
added thereto at room temperature. After being stirred for 24
hours, 55 .mu.L (0.77 mmol) of acetyl chloride was added to the
reaction mixture and then the mixture was confirmed to be
neutralized. After addition of water, the solution was extracted
with ethyl acetate. The extract was washed with saturated brine,
and dried over anhydrous sodium sulfate. After filtration, the
filtrate was concentrated, and the resulting residue was purified
by silica gel column chromatography (methanol/methylene chloride
mixture) to obtain 0.28 g of the title compound (7% yield in 2
steps) as a yellow viscous product. The results of NMR analysis of
the thus obtained compound are as shown below.
[0374] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.80 (m, 24H), 1.90-2.10 (m, 4H),
3.30-3.45 (m, 2H), 3.50-3.70 (m, 3H), 3.80-4.00 (m, 3H), 4.31 (d,
J=7.7 Hz, 1H), 5.10 (brs, 1H).
Example 25
Synthesis of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-galactoside
##STR00018##
[0376] The title compound was synthesized using the same procedure
as employed in Example 24, but with 3.0 g (7.7 mmol) of D-galactose
pentaacetate instead of .beta.-D-glucose pentaacetate, having the
following properties:
[0377] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 24H), 1.90-2.10 (m, 4H),
3.50-3.95 (m, 7H), 4.05 (brs, 1H), 4.25 (d, J=6.3 Hz, 1H), 5.10
(brs, 1H).
Example 26
Synthesis of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-mannoside
##STR00019##
[0379] The title compound was synthesized using the same procedure
as employed in Example 24, but with 3.0 g (7.7 mmol) of D-mannose
pentaacetate instead of .beta.-D-glucose pentaacetate, having the
following properties:
[0380] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 24H), 1.90-2.10 (m, 4H),
3.30-3.45 (m, 1H), 3.51 (d, J=9.1 Hz, 1H), 3.55-4.00 (m, 6H), 4.81
(s, 1H), 5.10 (brs, 1H).
Example 27
Synthesis of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-maltoside
##STR00020##
[0382] 2.7 g (4.0 mmol) of D-maltose octaacetate and 1.0 g (3.1
mmol) of 5,9,13,17-tetramethyloctadec-4-en-1-ol were dissolved in
dry acetonitrile (3 mL). 0.78 mL (6.2 mmol) of boron trifluoride
diethyl etherate complex was added to the solution with cooling on
ice. The reaction mixture was allowed to warm up slowly to room
temperature while being stirred overnight before addition of 1.3 mL
(9.2 mmol) of triethylamine at 0.degree. C. The resulting solution
was diluted with ethyl acetate, and washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over sodium sulfate.
After filtration, the filtrate was concentrated to obtain
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-maltoside heptaacetate
as a crude product.
[0383] The above crude product of
1-O-(5,9,13,17-tetramethyloctadec-4-enyl)-D-maltoside heptaacetate
was dissolved in methanol/tetrahydrofuran (1:1, 6 mL), and 0.31 mL
(0.31 mmol) of 1M sodium methylate in methanol was added at room
temperature. After being stirred for 24 hours, 22 .mu.L (0.31 mmol)
of acetyl chloride was added to the reaction mixture and then the
mixture was conformed to be neutralized. The solution was
concentrated, and the resulting residue was purified by silica gel
column chromatography (methanol/methylene chloride mixture) to
obtain the title compound. The results of NMR analysis of the thus
obtained compound are as shown below.
[0384] .sup.1H-NMR spectrum (300 MHz, CD.sub.3OD, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 24H), 1.90-2.15 (m, 4H),
3.10-3.95 (m, 14H), 4.26 (d, J=7.7 Hz, 1H), 4.61 (s, 1H), 5.14
(brs, 1H).
Example 28
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)dipentaerythritol
##STR00021##
[0386] 1.28 mL (9.23 mmol) of triethylamine, 1.06 g (5.56 mmol) of
p-toluenesulfonyl chloride, 43 mg (0.45 mmol) of trimethylamine
hydrochloride were added to a solution of 1.50 g (4.63 mmol) of
5,9,13,17-tetramethyloctadec-4-en-1-ol in dry methylene chloride (9
mL) was added, at 0.degree. C., sequentially. After being stirred
for 3 hours at room temperature, 0.14 mL (1.1 mmol) of
N,N-dimethyl-1,3-propanediamine was added to the reaction mixture
at 0.degree. C. After being stirred for 3 hours, the mixture was
diluted with ethyl acetate. The resulting solution was washed with
water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous
solution, and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated to obtain
(5,9,13,17-tetramethyloctadec-4-enyl)tosylate as a crude
product.
[0387] 0.37 g (60%, 9.2 mmol) of sodium hydride was added to a
solution of 2.35 g (9.24 mmol) of dipentaerythritol in dry
N,N-dimethylformamide (6 mL) with cooling on ice. After the mixture
was stirred for 1 hour at 50.degree. C., the above
(5,9,13,17-tetramethyloctadec-4-enyl)tosylate was added dropwise
thereto, with additional stirring for 20 hours at 60.degree. C.
After addition of water at 0.degree. C., the reaction mixture was
extracted with ethyl acetate. The extract was washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain 494 mg of the title
compound (19% yield in 2 steps) as a white solid. The results of
NMR analysis of the thus obtained compound are as shown below.
[0388] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3+3% CD.sub.3OD,
TMS) .delta.: 0.80-0.90 (m, 12H), 1.00-1.70 (m, 24H), 1.90-2.10 (m,
4H), 3.35-3.70 (in, 18H), 5.09 (t, J=6.6 Hz, 1H).
Example 29
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)sorbitol
##STR00022##
[0390] The title compound was synthesized using the same procedure
as employed in Example 28, but with 1.68 g (9.24 mmol) of sorbitol
instead of dipentaerythritol. The compound was obtained as a
colorless transparent viscous product (679 mg; 30% yield in 2
steps) having the following properties:
[0391] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 24H), 1.97-2.10 (m, 4H),
3.40-4.00 (m, 10H), 5.09 (brs, 1H).
Example 30
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)mannitol
##STR00023##
[0393] The title compound was synthesized using the same procedure
as employed in Example 28, but with 1.68 g (9.24 mmol) of mannitol
instead of dipentaerythritol. The compound was obtained as a yellow
viscous product (544 mg; 24% in 2 steps) having the following
properties:
[0394] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 24H), 1.90-2.10 (m, 4H),
3.20-3.95 (m, 10H), 5.08 (brs, 1H).
Example 31
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)glycerol
##STR00024##
[0396] The title compound was synthesized using the same procedure
as employed in Example 28, but with 0.851 g (9.24 mmol) of glycerol
instead of dipentaerythritol, having the following properties:
[0397] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 24H), 1.90-2.10 (m, 4H), 2.19
(dd, J=4.8, 7.2 Hz, 1H, OH), 2.63 (d, J=5.1 Hz, 1H, OH), 3.40-3.90
(m, 7H), 5.10 (t, J=7.2 Hz, 1H).
Example 32
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)diglycerol
##STR00025##
[0399] The title compound was synthesized using the same procedure
as employed in Example 28, but with 1.54 g (9.24 mmol) of
diglycerol instead of dipentaerythritol, having the following
properties:
[0400] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 24H), 1.90-2.10 (m, 4H),
3.40-4.00 (m, 12H), 5.10 (t, J=7.1 Hz, 1H).
Example 33
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)triglycerol
##STR00026##
[0402] The title compound was synthesized using the same procedure
as employed in Example 28, but with 2.22 g (9.24 mmol) of
triglycerol instead of dipentaerythritol, having the following
properties:
[0403] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 24H), 1.90-2.10 (m, 4H),
3.40-4.20 (m, 17H), 5.10 (brs, 1H).
Example 34
Synthesis of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)xylitol
##STR00027##
[0405] The title compound was synthesized using the same procedure
as employed in Example 28, but with 1.41 g (9.24 mmol) of xylitol
instead of dipentaerythritol, having the following properties:
[0406] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 24H), 1.90-2.10 (m, 4H), 3.49
(td, J=2.7, 6.6 Hz, 2H), 3.60 (d, J=4.4 Hz, 2H), 3.65-3.90 (m, 4H),
3.93 (m, 1H), 5.09 (t, J=7.5 Hz, 1H).
Example 35
Synthesis of mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)ascorbic
acid
##STR00028##
[0408] 1.28 mL (9.23 mmol) of triethylamine, 1.06 g (5.56 mmol) of
p-toluenesulfonyl chloride, 43 mg (0.45 mmol) of trimethylamine
hydrochloride were added to a solution of 1.50 g (4.63 mmol) of
5,9,13,17-tetramethyloctadec-4-en-1-ol in dry methylene chloride (9
mL) at 0.degree. C., sequentially. After being stirred for 3 hours
at room temperature, 0.14 mL (1.1 mmol) of
N,N-dimethyl-1,3-propanediamine was added to the reaction mixture
at 0.degree. C. After being stirred for 3 hours, the mixture was
diluted with ethyl acetate. The resulting solution was washed with
water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous
solution, and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated to obtain
(5,9,13,17-tetramethyloctadec-4-enyl)tosylate as a crude
product.
[0409] 0.71 mL (5.1 mmol) of triethylamine was added and dissolved
in a suspension of 0.82 g (4.63 mmol) of ascorbic acid in
acetonitrile (9 mL). The above crude product of
(5,9,13,17-tetramethyloctadec-4-enyl)tosylate was added at room
temperature, and the reaction mixture was heated for 2 hours at
90.degree. C. The reaction mixture was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 36
Synthesis of 3,7,11,15-tetramethylhexadec-2-ene-1-nitrile
##STR00029##
[0411] 90.1 g (0.674 mol) of N-Chlorosuccinimide was suspended in
methylene chloride (840 mL). After addition of 52.4 mL (0.708 mol)
of dimethylsulfide at 0.degree. C., the solution was stirred for 20
min. After addition of 100 g (0.337 mol) of phytol, the mixture was
stirred for 1 hour at 0.degree. C., with additional stirring for 6
hours at room temperature. The reaction mixture was diluted with
saturated sodium bicarbonate aqueous solution, and extracted with
methylene chloride. The extract was washed with saturated brine,
and dried over anhydrous sodium sulfate. After filtration, the
filtrate was concentrated to obtain
3,7,11,15-tetramethylhexadec-2-ene-1-chloride as a crude
product.
[0412] 19.8 g (0.405 mol) of sodium cyanide was added to a solution
of the thus obtained crude product in N,N-dimethylformamide (560
mL). The solution was stirred for 10 hours at room temperature.
After addition of water at 0.degree. C., the reaction mixture was
extracted with a mixed solvent of ether/hexane. The extract was
washed with saturated sodium bicarbonate aqueous solution and
saturated brine, successively, and dried over sodium sulfate. After
filtration, the filtrate was concentrated, and the resulting
residue was purified by silica gel column chromatography (ethyl
acetate/hexane mixture) to obtain 88.9 g of the title compound (86%
in 2 steps) as a yellow liquid. The results of NMR analysis of the
obtained compound are as shown below.
[0413] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.55 (m, 19H), 1.66 and 1.74 (s, 3H,
3-CH.sub.3), 2.00 (t, J=7.7 Hz, 2H), 3.04 (d, J=7.0 Hz, 2H), 5.16
(t, 0.1=7.0 Hz, 1H).
Example 37
Synthesis of methyl 4,8,12,16-tetramethylheptadec-3-enoate
##STR00030##
[0415] Water (115 mL) and 35.5 g (0.63 mol) of potassium hydroxide
were added to a solution of 77 g (0.25 mol) of
3,7,11,15-tetramethylhexadec-2-ene-1-nitrile in ethanol (345 mL).
The solution was stirred for 18 hours at 80.degree. C. The reaction
mixture was concentrated, and neutralized with 3M hydrochloric
acid, and then extracted with ethyl acetate. The extract was washed
with saturated brine, and dried over sodium sulfate. After
filtration, the filtrate was concentrated to obtain 88 g of
4,8,12,16-tetramethylheptadec-3-enoic acid as a crude product.
[0416] The thus obtained crude product of
4,8,12,16-tetramethylheptadec-3-enoic acid was dissolved in
methanol (400 mL), and concentrated sulfuric acid (8 mL) was added
at room temperature. After being stirred for 12 hours, sodium
bicarbonate was added slowly to the reaction mixture and the
mixture was confirmed to be neutralized. After filtration, the
filtrate was concentrated, and the residue was diluted with ethyl
acetate. The solution was washed with water and saturated brine,
successively, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated, and the resulting
residue was purified by silica gel column chromatography (ethyl
acetate/hexane mixture) to obtain 65.2 g of the title compound (77%
in 2 steps) as a slightly yellow liquid. The results of NMR
analysis of the obtained compound are as shown below.
[0417] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.62 and 1.73 (s, 3H,
4-CH.sub.3), 2.00 (t, J=7.5 Hz, 2H), 3.05 (d, J=6.5 Hz, 2H), 3.68
(s, 3H), 5.31 (t, J=6.5 Hz, 1H).
Example 38
Synthesis of 4,8,12,16-tetramethylheptadec-3-en-1-ol
##STR00031##
[0419] Under a nitrogen atmosphere, 9.8 g (0.26 mol) of lithium
aluminum hydride was added little by little at 0.degree. C. to a
solution of 35 g (0.10 mol) of methyl
4,8,12,16-tetramethylheptadec-3-enoate in dry tetrahydrofuran (250
mL). After being stirred at 50.degree. C. for 3 hours, the reaction
mixture was cooled on ice, followed by careful addition of
saturated sodium sulfate aqueous solution until the resulting gray
suspension turned white. Sodium sulfate was added to the solution
at room temperature for drying. After filtration, the filtrate was
concentrated to obtain 28.7 g of the title compound (92% yield) as
a colorless transparent liquid. The results of NMR analysis of the
obtained compound are as shown below.
[0420] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.64 and 1.72 (s, 3H,
4-CH.sub.3), 1.95-2.05 (m, 2H), 2.29 (td, J=6.5, 7.3 Hz, 2H), 3.63
(t, J=6.5 Hz, 2H), 5.12 (t, J=7.3 Hz, 1H).
Example 39
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)glycerol
##STR00032##
[0422] 1.0 g (3.0 mmol) of methyl
4,8,12,16-tetramethylheptadec-3-enoate was slowly added dropwise to
a solution of 0.68 g (7.4 mmol) of glycerol and 0.61 g (4.4 mmol)
of potassium carbonate in dry N,N-dimethylformamide (3.5 mL) at
100.degree. C. After the reaction mixture was stirred at
100.degree. C. for 18 hours, 1M hydrochloric acid was added. The
reaction solution was extracted with ether, and the extract was
washed with saturated sodium bicarbonate aqueous solution and
saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(ethyl acetate/hexane mixture) to obtain 347 mg of the title
compound (29% yield) as a yellow viscous product.
[0423] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0424] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.63 and 1.74 (s, 3H,
4-CH.sub.3), 2.00 (t, J=7.4 Hz, 2H), 3.10 (d, J=7.2 Hz, 2H),
3.55-4.00 (m, 3H), 4.10-4.30 (m, 2H), 5.30 (t, J=7.21 Hz, 1H).
Example 40
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)erythritol
##STR00033##
[0426] The title compound was synthesized using the same procedure
as employed in Example 39, but with 0.90 g (7.4 mmol) of erythritol
instead of glycerol. The compound was obtained (270 mg, 21% yield)
having the following properties:
[0427] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.63 and 1.74 (s, 3H,
4-CH.sub.3), 2.00 (t, J=7.8 Hz, 2H), 2.13 (brs, 1H, OH), 2.67 (d,
J=5.3 Hz, 1H, OH), 2.80 (d, J=5.8 Hz, 1H, OH), 3.12 (d, J=7.2 Hz,
2H), 3.65-3.95 (m, 4H), 4.30-4.40 (m, 2H), 5.31 (t, J=7.2 Hz,
1H).
Example 41
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)pentaerythritol
##STR00034##
[0429] The title compound was synthesized using the same procedure
as employed in Example 39, but with 1.0 g (7.4 mmol) of
pentaerythritol instead of glycerol. The compound was obtained (408
mg, 32% yield) having the following properties:
[0430] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.64 and 1.74 (s, 3H,
4-CH.sub.3), 2.00 (t, J=7.4 Hz, 2H), 2.56 (brs, 3H, OH), 3.10 (d,
J=7.2 Hz, 2H), 3.64 (brs, 6H), 4.23 (s, 2H), 5.29 (t, J=7.2 Hz,
1H).
Example 42
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)diglycerol
##STR00035##
[0432] 1.0 g (3.0 mmol) of methyl
4,8,12,16-tetramethylheptadec-3-enoate was slowly added dropwise to
a solution of 1.23 g (4.38 mmol) of diglycerol and 0.61 g (4.4
mmol) of potassium carbonate in dry N,N-dimethylformamide (3.5 mL)
at 100.degree. C. After the reaction mixture was stirred at
100.degree. C. for 18 hours, 1M hydrochloric acid was added. The
reaction solution was extracted with ethyl acetate, and the extract
was washed with saturated sodium bicarbonate aqueous solution and
saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain 153 mg of the title
compound (11% yield).
[0433] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0434] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.62 and 1.73 (s, 3H,
4-CH.sub.3), 2.02 (t, J=7.8 Hz, 2H), 3.09 (d, J=7.0 Hz, 2H),
3.50-4.30 (m, 10H), 5.31 (t, J=7.0 Hz, 1H).
Example 43
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)triglycerol
##STR00036##
[0436] The title compound was synthesized using the same procedure
as employed in Example 42, but with 1.77 g (7.38 mmol) of
triglycerol instead of diglycerol. The compound was obtained (138
mg, 8% yield) having the following properties:
[0437] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.62 and 1.73 (s, 3H,
4-CH.sub.3), 1.99 (t, J=7.1 Hz, 2H), 3.09 (d, J=6.9 Hz, 2H),
3.50-4.25 (m, 15H), 5.31 (t, J=6.9 Hz, 1H).
Example 44
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)xylitol
##STR00037##
[0439] The title compound was synthesized using the same procedure
as employed in Example 42, but with 1.12 g (7.38 mmol) of xylitol
instead of diglycerol. The compound was obtained (215 mg, 16%
yield) having the following properties:
[0440] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.62 and 1.74 (s, 3H,
4-CH.sub.3), 2.00 (t, J=7.6 Hz, 2H), 3.10 (d, J=7.1 Hz, 2H),
3.60-4.10 (m, 5H), 4.24 (d, J=5.7 Hz, 2H), 5.29 (t, J=7.1 Hz,
1H).
Example 45
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)mannitol
##STR00038##
[0442] The title compound was synthesized using the same procedure
as employed in Example 42, but with 1.35 g (7.38 mmol) of mannitol
instead of diglycerol. The compound was obtained (375 mg, 26%
yield) having the following properties:
[0443] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.55 (m, 19H), 1.60 and 1.72 (s, 3H,
4-CH.sub.3), 1.97 (brt, 2H), 3.11 (d, J=5.7 Hz, 2H), 3.60-4.50 (m,
8H), 5.29 (t, J=5.7 Hz, 1H).
Example 46
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)sorbitol
##STR00039##
[0445] The title compound was synthesized using the same procedure
as employed in Example 42, but with 1.35 g (7.38 mmol) of sorbitol
instead of diglycerol. The compound was obtained (310 mg, 21%
yield) having the following properties:
[0446] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.61 and 1.72 (s, 3H,
4-CH.sub.3), 1.98 (brt, 2H), 3.10 (brs, 2H), 3.60-4.50 (m, 8H),
5.29 (brs, 1H).
Example 47
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)dipentaerythritol
##STR00040##
[0448] The title compound was synthesized using the same procedure
as employed in Example 42, but with 1.88 g (7.38 mmol) of
dipentaerythritol instead of diglycerol. The compound was obtained
(144 mg, 9% yield) having the following properties:
[0449] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.63 and 1.74 (s, 3H,
4-CH.sub.3), 2.00 (t, J=7.8 Hz, 2H), 3.08 (d, J=7.0 Hz, 2H), 3.38
(d, J=8.3 Hz, 4H), 3.50-3.60 (m, 10H), 4.07 (s, 2H), 5.28 (t, J=7.0
Hz, 1H).
Example 48
Synthesis of mono-O-(4,8,12,16-tetramethylheptadec-3-enoyl)ascorbic
acid
##STR00041##
[0451] 0.53 g (3.0 mmol) of ascorbic acid was dissolved in
concentrated sulfuric acid (14 mL). After addition of 1.0 g (3.0
mmol) of methyl 4,8,12,16-tetramethylheptadec-3-enoate, the mixture
was stirred for 24 hours at room temperature. The reaction mixture
was poured into iced water, and extracted with ethyl acetate. The
extract was washed with water, 1M hydrochloric acid, saturated
sodium bicarbonate aqueous solution, and saturated brine,
successively, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated, and the resulting
residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 49
Synthesis of
1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-glucoside
##STR00042##
[0453] 1.63 g (4.19 mmol) of .beta.-D-Glucose pentaacetate and 1.0
g (3.2 mmol) of 4,8,12,16-tetramethylheptadec-3-en-1-ol were
dissolved in dry acetonitrile (3 mL). 0.82 mL (6.4 mmol) of boron
trifluoride diethyl etherate complex was added to the solution with
cooling on ice. The reaction mixture was allowed to warm up slowly
to room temperature while being stirred for 18 hours before
addition of 1.3 mL (9.7 mmol) of triethylamine at 0.degree. C. The
resulting solution was diluted with ethyl acetate, and washed with
water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous
solution, and saturated brine, successively, and dried over sodium
sulfate. After filtration, the filtrate was concentrated to obtain
1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-glucopyranoside
tetraacetate as a crude product.
[0454] The above obtained crude product of
1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-glucopyranoside
tetraacetate was dissolved in methanol/tetrahydrofuran (1:1, 6 mL),
and 0.32 mL (0.32 mmol) of 1M sodium methylate in methanol was
added at room temperature. After being stirred for 24 hours, 254
(0.35 mmol) of acetyl chloride was added to the reaction mixture
and the mixture was confirmed to be neutralized. After addition of
water, the solution was extracted with ethyl acetate. The extract
was washed with saturated brine, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title compound.
The results of NMR analysis of the obtained compound are as shown
below.
[0455] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.80 (m, 22H), 1.90-2.15 (m, 4H),
3.30-3.90 (m, 8H), 4.31 (brs, 1H), 5.13 (brs, 1H).
Example 50
Synthesis of
1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-xylopyranoside
##STR00043##
[0457] The title compound was synthesized using the same procedure
as employed in Example 49, but with 1.33 g (4.19 mmol) of D-xylose
tetraacetate instead of .beta.-D-glucose pentaacetate, having the
following properties:
[0458] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.80 (m, 22H), 1.85-2.15 (m, 4H),
3.30-4.10 (m, 7H), 4.38 (d, J=5.1 Hz, 0.5H), 4.89 (d, d=3.9 Hz,
0.5H), 5.11 (t, J=6.0 Hz, 1H).
Example 51
Synthesis of
1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-galactoside
##STR00044##
[0460] The title compound was synthesized using the same procedure
as employed in Example 49, but with 1.63 g (4.19 mmol) of
D-galactose pentaacetate instead of .beta.-D-glucose pentaacetate,
having the following properties:
[0461] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.80 (m, 22H), 1.85-2.10 (m, 4H),
3.40-4.10 (m, 9H), 4.26 (brs, 1H), 5.00-5.10 (m, 1H).
Example 52
Synthesis of
1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-mannoside
##STR00045##
[0463] The title compound was synthesized using the same procedure
as employed in Example 49, but with 1.63 g (4.19 mmol) of D-mannose
pentaacetate instead of .beta.-D-glucose pentaacetate, having the
following properties:
[0464] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.85 (m, 22H), 1.85-2.05 (m, 4H),
3.30-4.20 (m, 8H), 4.79 (d, J=7.2 Hz, 1H), 5.07 (brs, 1H).
Example 53
Synthesis of
1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-maltoside
##STR00046##
[0466] 2.84 g (4.19 mmol) of D-maltose octaacetate and 1.0 g (3.2
mmol) of 4,8,12,16-tetramethylheptadec-3-en-1-ol was dissolved in
dry acetonitrile (3 mL). 0.82 mL (6.4 mmol) of boron trifluoride
diethyl etherate complex was added to the solution with cooling on
ice. The reaction mixture was allowed to warm up slowly to room
temperature while being stirred 18 hours before addition of 1.34 mL
(9.66 mmol) of triethylamine at 0.degree. C. The resulting solution
was diluted with ethyl acetate, and washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over sodium sulfate.
After filtration, the filtrate was concentrated to obtain
1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-maltoside heptaacetate
as a crude product.
[0467] The above obtained crude product of
1-O-(4,8,12,16-tetramethylheptadec-3-enyl)-D-maltoside heptaacetate
was dissolved in methanol/tetrahydrofuran (1:1, 4 mL), and 0.42 mL
(0.42 mmol) of 1M sodium methylate in methanol was added at room
temperature. After being stirred for 24 hours, 55 .mu.L (0.77 mmol)
of acetyl chloride was added to the reaction mixture and the
mixture was confirmed to be neutralized. The solution was
concentrated, and the resulting residue was purified by silica gel
column chromatography (methanol/methylene chloride mixture) to
obtain the title compound. The results of NMR analysis of the
obtained compound are as shown below.
[0468] .sup.1H-NMR spectrum (300 MHz, CD.sub.3OD, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 22H), 1.90-2.10 (m, 4H),
3.15-3.90 (m, 14H), 4.20-4.30 (m, 1H), 4.60 (brs, 1H), 5.13 (brs,
2H).
Example 54
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)glycerol
##STR00047##
[0470] Under a nitrogen atmosphere, 0.49 mL (3.5 mmol) of
triethylamine, 0.68 g (3.54 mmol) of p-toluenesulfonyl chloride,
and 15 mg (0.16 mmol) of trimethylamine hydrochloride were added to
a solution of 1.0 g (3.2 mmol) of
4,8,12,16-tetramethylheptadec-3-en-1-ol in dry methylene chloride
(3.2 mL) at 0.degree. C., sequentially. After being stirred for 2
hours at room temperature, 0.080 mL (0.64 mmol) of
N,N-dimethyl-1,3-propanediamine was added to the reaction mixture
at 0.degree. C. After being stirred for 15 min, water was added,
and the mixture was extracted with methylene chloride. The extract
was washed with 1M hydrochloric acid, saturated sodium bicarbonate
aqueous solution, and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated to obtain
(4,8,12,16-tetramethylheptadec-3-enyl)tosylate as a crude
product.
[0471] 0.21 g (55%, 4.8 mmol) of sodium hydride was added to a
solution of 0.44 g (4.8 mmol) of glycerol in dry
N,N-dimethylformamide (5 mL) with cooling on ice. After the mixture
was stirred for 30 min at 50.degree. C., the above
(4,8,12,16-tetramethylheptadec-3-enyl)tosylate was added dropwise
with additional stirring for 12 hours at the same temperature.
After addition of water at 0.degree. C., the reaction mixture was
extracted with ethyl acetate. The extract was washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
residue was purified by silica gel column chromatography (ethyl
acetate/hexane mixture) to obtain 44 mg of the title compound (4%
yield in 2 steps) as a colorless transparent viscous product. The
results of NMR analysis of the obtained compound are as shown
below.
[0472] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.61 and 1.69 (s, 3H,
4-CH.sub.3), 1.96 (t, J=7.6 Hz, 2H), 2.30 (m, 2H), 3.40-3.90 (m,
7H), 5.12 (m, 1H).
Example 55
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)erythritol
##STR00048##
[0474] The title compound was synthesized using the same procedure
as employed in Example 54, but with 0.59 g (4.8 mmol) of erythritol
instead of glycerol, having the following properties:
[0475] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.61 and 1.69 (s, 3H,
4-CH.sub.3), 1.90-2.05 (m, 2H), 2.29 (td, J=6.5 Hz, 2H), 2.64 (brs,
1H, OH), 2.74 (brs, 1H, OH), 3.45-3.51 (m, 2H), 3.55-3.68 (m, 2H),
3.70-3.85 (m, 4H), 5.10 (t, J=6.5 Hz, 1H).
Example 56
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)pentaerythritol
##STR00049##
[0477] The title compound was synthesized using the same procedure
as employed in Example 54, but with 0.66 g (4.8 mmol) of
pentaerythritol instead of glycerol. The compound was obtained (193
mg, 17% yield in 2 steps) having the following properties:
[0478] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.61 and 1.69 (s, 3H,
4-CH.sub.3), 1.96 (t, J=8.0 Hz, 2H), 2.28 (td, J=6.9 Hz, 2H), 2.49
(t, J=5.1 Hz, 3H, OH), 3.35-3.50 (m, 4H), 3.71 (d, J=5.1 Hz, 6H),
5.09 (t, J=6.9 Hz, 1H).
Example 57
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)diglycerol
##STR00050##
[0480] 0.49 mL (3.5 mmol) of triethylamine, 0.68 g (3.54 mmol) of
p-toluenesulfonyl chloride, 15 mg (0.16 mmol) of trimethylamine
hydrochloride were added to a solution of 1.0 g (3.2 mmol) of
4,8,12,16-tetramethylheptadec-3-en-1-ol in dry methylene chloride
(3.2 mL) at 0.degree. C., sequentially. After being stirred for 2
hours at room temperature, 0.080 mL (0.64 mmol) of
N,N-dimethyl-1,3-propanediamine was added to the reaction mixture
at 0.degree. C. After being stirred for 15 min, water was added,
and the mixture was extracted with methylene chloride. The extract
was washed with 1M hydrochloric acid, saturated sodium bicarbonate
aqueous solution, and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated to obtain
(4,8,12,16-tetramethylheptadec-3-enyl)tosylate as a crude product.
0.21 g (55%, 4.8 mmol) of sodium hydride was added to a solution of
0.80 g (4.8 mmol) of diglycerol in dry N,N-dimethylformamide (5 mL)
with cooling on ice. After the mixture was stirred for 30 min at
50.degree. C., the above
(4,8,12,16-tetramethylheptadec-3-enyl)tosylate was added dropwise
with additional stirring for 12 hours at the same temperature.
After addition of water at 0.degree. C., the reaction mixture was
extracted with ethyl acetate. The extract was washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain 312 mg of the title
compound (25% yield in 2 steps). The results of NMR analysis of the
obtained compound are as shown below.
[0481] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.61 and 1.69 (s, 3H,
4-CH.sub.3), 1.90-2.05 (m, 2H), 2.25-2.35 (m, 2H), 3.40-4.00 (m,
12H), 5.10 (brs, 1H).
Example 58
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)triglycerol
##STR00051##
[0483] The title compound was synthesized using the same procedure
as employed in Example 57, but with 1.16 g (4.83 mmol) of
triglycerol instead of diglycerol. The compound was obtained (310
mg, 21% yield in 2 steps) having the following properties:
[0484] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.61 and 1.69 (s, 3H,
4-CH.sub.3), 1.95 (m, 2H), 2.29 (m, 2H), 3.40-4.05 (m, 17H), 5.10
(brs, 1H).
Example 59
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)xylitol
##STR00052##
[0486] The title compound was synthesized using the same procedure
as employed in Example 57, but with 0.73 g (4.8 mmol) of xylitol
instead of diglycerol, having the following properties:
[0487] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 22H), 1.94 (m, 2H), 2.20 (m, 2H),
3.00-3.80 (m, 9H), 5.01 (brs, 1H).
Example 60
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)mannitol
##STR00053##
[0489] The title compound was synthesized using the same procedure
as employed in Example 57, but with 0.88 g (4.8 mmol) of mannitol
instead of diglycerol. The compound was obtained (97 mg, 8% yield
in 2 steps) having the following properties:
[0490] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 1.61 and 1.69 (s, 3H,
4-CH.sub.3), 1.94 (m, 2H), 2.31 (m, 2H), 3.45-3.95 (m, 10H), 5.08
(brs, 1H).
Example 61
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)sorbitol
##STR00054##
[0492] The title compound was synthesized using the same procedure
as employed in Example 57, but with 0.88 g (4.8 mmol) of sorbitol
instead of diglycerol. The compound was obtained (126 mg, 10% yield
in 2 steps) having the following properties:
[0493] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 22H), 1.94 (m, 2H), 2.27 (m, 2H),
3.20-4.00 (m, 10H), 5.08 (brs, 1H).
Example 62
Synthesis of
mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)dipentaerythritol
##STR00055##
[0495] The title compound was synthesized using the same procedure
as employed in Example 57, but with 1.23 g (4.83 mmol) of
dipentaerythritol instead of diglycerol. The compound was obtained
(133 mg, 6% yield in 2 steps) having the following properties:
[0496] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.58 (m, 19H), 1.60 and 1.69 (s, 3H,
4-CH.sub.3), 1.95 (t, J=7.7 Hz, 2H), 2.26 (td, J=6.3 Hz, 2H),
3.35-3.48 (m, 8H), 3.50-3.65 (m, 10H), 5.08 (t, J=6.3 Hz, 1H).
Example 63
Synthesis of mono-O-(4,8,12,16-tetramethylheptadec-3-enyl)ascorbic
acid
##STR00056##
[0498] 0.49 mL (3.5 mmol) of triethylamine, 0.68 g (3.54 mmol) of
p-toluenesulfonyl chloride, 15 mg (0.16 mmol) of trimethylamine
hydrochloride were added to a solution of 1.0 g (3.2 mmol) of
4,8,12,16-tetramethylheptadec-3-en-1-ol in dry methylene chloride
(3.2 mL) at 0.degree. C., sequentially. After being stirred for 2
hours at room temperature, 0.080 mL (0.64 mmol) of
N,N-dimethyl-1,3-propanediamine was added to the reaction mixture
at 0.degree. C. After being stirred for 15 min, water was added,
and the mixture was extracted with methylene chloride. The extract
was washed with 1M hydrochloric acid, saturated sodium bicarbonate
aqueous solution, and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated to obtain
(4,8,12,16-tetramethylheptadec-3-enyl)tosylate as a crude
product.
[0499] 0.49 mL (3.5 mmol) of triethylamine was added and dissolved
in a suspension of 0.56 g (3.2 mmol) of ascorbic acid in
acetonitrile (7 mL). After the above crude product of
(4,8,12,16-tetramethylheptadec-3-enyl)tosylate was added at room
temperature, the reaction mixture was heated for 2 hours at
90.degree. C. The reaction mixture was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 64
Synthesis of methyl 3,7,11,15-tetramethylhexadec-2-enoate
##STR00057##
[0501] Under a nitrogen atmosphere, 17.4 mL (202 mmol) of oxalyl
chloride was dissolved in methylene chloride (300 mL). 36 mL (0.51
mol) of dimethyl sulfoxide was slowly added dropwise to the mixture
at -78.degree. C. After the mixture was stirred for 15 min, 50 g
(0.17 mol) of phytol was added, followed by stirring for 1 hour at
the same temperature. After addition of 94 mL (0.68 mol) of
triethylamine, the reaction mixture was allowed to warm up to room
temperature. The mixture was concentrated with methylene chloride,
and the residue was diluted with diethylether, and the solution was
washed saturated brine, and dried over anhydrous sodium sulfate.
After filtration, the filtrate was concentrated to obtain
3,7,11,15-tetramethylhexadec-2-en-1-al as a crude product.
[0502] The above obtained crude product of
3,7,11,15-tetramethylhexadec-2-en-1-al was dissolved in t-butanol
(150 mL) and water (150 mL). 52.7 g (0.338 mmol) of sodium
dihydrogen phosphate, 21 g (0.22 mmol) of amidosulfuric acid, and
19.6 g (0.216 mmol) of sodium chlorite were added to the solution.
After being stirred for 18 hours at room temperature, the reaction
mixture was diluted with ether. The solution was washed with water
and saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated to obtain
3,7,11,15-tetramethylhexadec-2-enoic acid as a crude product.
[0503] The above obtained crude product of
3,7,11,15-tetramethylhexadec-2-enoic acid was dissolved in methanol
(300 mL), and concentrated sulfuric acid (3 mL) was added and
stirred for 18 hours at 55.degree. C. Sodium bicarbonate was slowly
added to the reaction solution and confirmed to be neutralized.
After filtration, the filtrate was concentrated, and diluted with
ethyl acetate. The solution was washed with water and saturated
brine, successively, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated, and the resulting
residue was purified by silica gel column chromatography (ethyl
acetate/hexane mixture) to obtain 32.2 g of the title compound (59%
in 3 steps) as a slightly yellow liquid. The results of NMR
analysis of the obtained compound are as shown below.
[0504] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.60 (m, 19H), 2.00-2.20 (m, 5H), 3.69 (s,
3H), 5.67 (s, 1H).
Example 65
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)glycerol
##STR00058##
[0506] 1.0 g (3.1 mmol) of methyl
3,7,11,15-tetramethylhexadec-2-enoate was added dropwise to a
solution of 0.57 g (6.2 mmol) of glycerol and 0.85 g (6.2 mmol) of
potassium carbonate in dry N,N-dimethylformamide (3 mL) at
80.degree. C. After the reaction mixture was stirred at 100.degree.
C. for 12 hours, 1M hydrochloric acid was added. The resulting
solution was extracted with ether, and the extract was washed with
saturated sodium bicarbonate aqueous solution and saturated brine,
successively, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated, and the resulting
residue was purified by silica gel column chromatography (ethyl
acetate/hexane mixture) to obtain 459 mg of the title compound (35%
yield) as a colorless viscous product.
[0507] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0508] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (in, 12H), 1.00-1.80 (m, 19H), 1.90-2.20 (m, 5H),
3.50-4.00 (m, 3H), 4.10-4.30 (m, 2H), 5.71 (brs, 1H).
Example 66
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)erythritol
##STR00059##
[0510] The title compound was synthesized using the same procedure
as employed in Example 65, but with 0.76 g (6.2 mmol) of erythritol
instead of glycerol. The compound was obtained (378 mg, 27% yield)
having the following properties:
[0511] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 12H), 1.00-1.80 (m, 19H), 1.90-2.20 (m, 5H),
3.55-4.00 (m, 4H), 4.25-4.45 (m, 2H), 5.72 (brs, 1H).
Example 67
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)pentaerythritol
##STR00060##
[0513] The title compound was synthesized using the same procedure
as employed in Example 65, but with 0.84 g (6.2 mmol) of
pentaerythritol instead of glycerol. The compound was obtained (537
mg, 37% yield) having the following properties:
[0514] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 12H), 1.00-1.60 (m, 19H), 1.90-2.20 (m, 5H), 2.71
(brs, 30H), 3.65 (s, 6H), 4.25 (brs, 2H), 5.70 (brs, 1H).
Example 68
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)diglycerol
##STR00061##
[0516] The title compound was synthesized using the same procedure
as employed in Example 65, but with 1.03 g (6.2 mmol) of diglycerol
instead of glycerol. The compound was obtained (388 mg, 25% yield)
having the following properties:
[0517] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.80 (m, 19H), 1.91 and 2.16 (s, 3H,
3-CH.sub.3), 2.10-2.20 (m, 2H), 3.50-3.95 (m, 7H), 4.00-4.30 (m,
3H), 5.71 (brs, 1H).
Example 69
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)xylitol
##STR00062##
[0519] The title compound was synthesized using the same procedure
as employed in Example 65, but with 0.94 g (6.2 mmol) of xylitol
instead of glycerol. The compound was obtained (219 mg, 15% yield)
having the following properties:
[0520] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.80 (m, 19H), 1.90 and 2.16 (s, 3H,
3-CH.sub.3), 2.10-2.20 (m, 2H), 3.60-4.10 (m, 5H), 4.20-4.30 (m,
2H), 5.70 (brs, 1H).
Example 70
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)triglycerol
##STR00063##
[0522] 1.0 g (3.1 mmol) of methyl
3,7,11,15-tetramethylhexadec-2-enoate was added slowly dropwise to
a solution of 1.49 g (6.2 mmol) of triglycerol and 0.85 g (6.2
mmol) of potassium carbonate in dry N,N-dimethylformamide (3 mL) at
100.degree. C. After the reaction mixture was stirred at
100.degree. C. for 15 hours, 1M hydrochloric acid was added. The
reaction solution was extracted with ethyl acetate, and the extract
was washed with saturated sodium bicarbonate aqueous solution and
saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain 369 mg of the title
compound (20% yield).
[0523] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0524] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 12H), 1.00-1.80 (m, 19H), 1.85-120 (m, 5H), 3.40-4.20
(m, 15H), 5.70 (brs, 1H).
Example 71
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)mannitol
##STR00064##
[0526] The title compound was synthesized using the same procedure
as employed in Example 70, but with 1.13 g (6.2 mmol) of mannitol
instead of triglycerol. The compound was obtained (177 mg, 11%
yield) having the following properties:
[0527] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.90 (m, 22H), 2.10-2.20 (m, 2H),
3.70-4.25 (m, 8H), 5.72 (s, 1H).
Example 72
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)sorbitol
##STR00065##
[0529] The title compound was synthesized using the same procedure
as employed in Example 70, but with 1.13 g (6.2 mmol) of sorbitol
instead of triglycerol. The compound was obtained (215 mg, 13%
yield) having the following properties:
[0530] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.80 (m, 19H), 1.80-2.30 (m, 5H),
3.60-4.50 (m, 8H), 5.70 (brs, 1H).
Example 73
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)dipentaerythritol
##STR00066##
[0532] The title compound was synthesized using the same procedure
as employed in Example 70, but with 1.58 g (6.2 mmol) of
dipentaerythritol instead of triglycerol. The compound was obtained
(106 mg, 6% yield) having the following properties:
[0533] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.80 (m, 19H), 1.91 and 2.16 (s, 3H,
3-CH.sub.3), 2.10-2.20 (m, 2H), 3.30-3.80 (m, 14H), 4.15 (s, 2H),
5.68 (brs, 1H).
Example 74
Synthesis of mono-O-(3,7,11,15-tetramethylhexadec-2-enoyl)ascorbic
acid
##STR00067##
[0535] 0.55 g (3.1 mmol) of ascorbic acid was dissolved in
concentrated sulfuric acid (14 mL). After addition of 1.0 g (3.1
mmol) of methyl 3,7,11,15-tetramethylhexadec-2-enoate, the mixture
was stirred for 24 hours at room temperature. The reaction mixture
was poured into iced water, and extracted with ethyl acetate. The
extract was washed with water, 1M hydrochloric acid, saturated
sodium bicarbonate aqueous solution, and saturated brine,
successively, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated, and the resulting
residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 75
Synthesis of
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-glucoside
##STR00068##
[0537] 3.4 g (8.7 mmol) of .beta.-D-Glucose pentaacetate and 2.0 g
(6.7 mmol) of phytol were dissolved in dry acetonitrile (7 mL).
1.70 mL (13.4 mmol) of boron trifluoride diethyl etherate complex
was added to the solution with cooling on ice. The reaction mixture
was allowed to warm up slowly to room temperature while being
stirred for 18 hours before addition of 2.8 mL (20 mmol) of
triethylamine at 0.degree. C. The resulting solution was diluted
with ethyl acetate, and washed with water, 1M hydrochloric acid,
saturated sodium bicarbonate aqueous solution, and saturated brine,
successively, and dried over sodium sulfate. After filtration, the
filtrate was concentrated to obtain a crude product of
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-glucopyranoside
tetraacetate.
[0538] The above obtained crude product of
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-glucopyranoside
tetraacetate was dissolved in methanol/tetrahydrofuran (1:1, 6 mL),
and 0.67 mL (0.67 mmol) of 1M sodium methylate in methanol was
added at room temperature. After being stirred for 24 hours, 48
.mu.L (0.67 mmol) of acetyl chloride was added to the reaction
mixture and the mixture was confirmed to be neutralized. After
addition of water, the solution was extracted with ethyl acetate.
The extract was washed with saturated brine, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated, and the resulting residue was purified by silica gel
column chromatography (methanol/methylene chloride mixture) to
obtain the title compound.
Example 76
Synthesis of
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-xylopyranoside
##STR00069##
[0540] The title compound was synthesized using the same procedure
as employed in Example 75, but with 2.8 g (8.7 mmol) of D-xylose
tetraacetate instead of .beta.-D-glucose pentaacetate.
Example 77
Synthesis of
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-galactoside
##STR00070##
[0542] The title compound was synthesized using the same procedure
as employed in Example 75, but with 3.4 g (8.7 mmol) of D-galactose
pentaacetate instead of 3-D-glucose pentaacetate.
Example 78
Synthesis of
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-mannoside
##STR00071##
[0544] The title compound was synthesized using the same procedure
as employed in Example 75, but with 3.4 g (8.7 mmol) of D-mannose
pentaacetate instead of 3-D-glucose pentaacetate.
Example 79
Synthesis of
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-maltoside
##STR00072##
[0546] 5.9 g (8.7 mmol) of D-Maltose octaacetate and 2.0 g (6.7
mmol) of phytol were dissolved in dry acetonitrile (7 mL). 1.70 mL
(13.4 mmol) of boron trifluoride diethyl etherate complex was added
with cooling on ice. The reaction mixture was allowed to warm up
slowly to room temperature while being stirred for 18 hours before
addition of 2.8 mL (20 mmol) of triethylamine at 0.degree. C. The
resulting solution was diluted with ethyl acetate, and washed with
water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous
solution, and saturated brine, successively, and dried over sodium
sulfate. After filtration, the filtrate was concentrated to obtain
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-maltoside heptaacetate
as a crude product.
[0547] The above obtained crude product of
1-O-(3,7,11,15-tetramethylhexadec-2-enyl)-D-maltoside heptaacetate
was dissolved in methanol/tetrahydrofuran (1:1, 6 mL), and 0.67 mL
(0.67 mmol) of 1M sodium methylate in methanol was added at room
temperature, and stirred for 24 hours. 48 .mu.L (0.67 mmol) of
acetyl chloride was added to the reaction mixture and the mixture
was confirmed to be neutralized. The resulting mixture was
concentrated, and the resulting residue was purified by silica gel
column chromatography (methanol/methylene chloride mixture) to
obtain the title compound.
Example 80
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)glycerol
##STR00073##
[0549] 0.90 g (6.7 mmol) of N-Chlorosuccinimide was suspended in
methylene chloride (8 mL). After addition of 0.52 mL (7.1 mmol) of
dimethylsulfide at 0.degree. C., the solution was stirred for 20
min. After addition of 1.0 g (3.4 mmol) of phytol, the mixture was
stirred for 1 hour at 0.degree. C., with additional stirring for 6
hours at room temperature. After addition of sodium bicarbonate
aqueous solution, the reaction mixture was extracted with methylene
chloride. The extract was washed with saturated brine, and dried
over anhydrous sodium sulfate. After filtration, the filtrate was
concentrated to obtain
3,7,11,15-tetramethylhexadec-2-ene-1-chloride as a crude
product.
[0550] 0.20 g (60%, 5.1 mmol) of sodium hydride was added to a
solution of 0.47 g (5.1 mmol) of glycerol in dry
N,N-dimethylformamide/tetrahydrofuran (1:1, 4 mL) with cooling on
ice. After the mixture was stirred for 30 min at 50.degree. C., the
above 3,7,11,15-tetramethylhexadec-2-ene-1-chloride was added
dropwise with additional stirring for 20 hours at the same
temperature. After addition of water at 0.degree. C., the reaction
mixture was extracted with ether. The extract was washed with
water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous
solution, and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated, and the resulting residue was purified by silica gel
column chromatography (ethyl acetate/hexane mixture) to obtain the
title compound. The results of NMR analysis of the obtained
compound are as shown below.
[0551] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.80 (m, 22H), 2.00 (t, J=8.2 Hz, 2H),
2.16 (brs, 1H, OH), 2.61 (brs, 1H, OH), 3.45-3.80 (m, 4H),
3.82-4.05 (m, 3H), 5.33 (t, J=6.2 Hz, 1H).
Example 81
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)erythritol
##STR00074##
[0553] The title compound was synthesized using the same procedure
as employed in Example 80, but with 0.62 g (5.1 mmol) of erythritol
instead of glycerol. The compound was obtained having the following
properties:
[0554] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.80 (m, 22H), 2.00 (t, J=8.6 Hz, 2H),
2.34 (brs, 1H, OH), 2.68 (brd, 1H, OH), 2.78 (brd, 1H, OH),
3.50-3.90 (m, 6H), 4.00-4.20 (m, 2H), 5.32 (brs, 1H).
Example 82
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)pentaerythritol
##STR00075##
[0556] The title compound was synthesized using the same procedure
as employed in Example 80, but with 0.69 g (5.1 mmol) of
pentaerythritol instead of glycerol. The compound was obtained
having the following properties:
[0557] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.75 (m, 22H), 1.90-2.05 (m, 2H), 2.60
(brs, 3H, OH), 3.46 (s, 2H), 3.72 (s, 6H), 3.98 (d, J=6.7 Hz, 2H),
5.29 (t, J=6.7 Hz, 1H).
Example 83
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)diglycerol
##STR00076##
[0559] The title compound was synthesized using the same procedure
as employed in Example 80, but with 0.85 g (5.1 mmol) of diglycerol
instead of glycerol.
Example 84
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)triglycerol
##STR00077##
[0561] 0.90 g (6.7 mmol) of N-Chlorosuccinimide was suspended in
methylene chloride (8 mL). After addition of 0.52 mL (7.1 mmol) of
dimethylsulfide at 0.degree. C., the solution was stirred for 20
min. After addition of 1.0 g (3.4 mmol) of phytol, the mixture was
stirred for 1 hour at 0.degree. C., with additional stirring for 6
hours at room temperature. After addition of saturated sodium
bicarbonate aqueous solution, the reaction mixture was extracted
with methylene chloride. The extract was washed with saturated
brine, and dried over anhydrous sodium sulfate. After filtration,
the filtrate was concentrated to obtain
3,7,11,15-tetramethylhexadec-2-ene-1-chloride as a crude
product.
[0562] 0.20 g (60%, 5.1 mmol) of sodium hydride was added to a
solution of 0.47 g (5.1 mmol) of triglycerol in dry
N,N-dimethylformamide/tetrahydrofuran (1:1, 4 mL) will cooling on
ice. After the mixture was stirred for 30 min at 50.degree. C., the
above 3,7,11,15-tetramethylhexadec-2-ene-1-chloride was added
dropwise, with additional stirring for 20 hours at the same
temperature. After addition of water at 0.degree. C., the reaction
mixture was extracted with ethyl acetate. The extract was washed
with water, 1M hydrochloric acid, saturated sodium bicarbonate
aqueous solution, and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated, and the resulting residue was purified by silica gel
column chromatography (methanol/methylene chloride mixture) to
obtain the title compound.
Example 85
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)xylitol
##STR00078##
[0564] The title compound was synthesized using the same procedure
as employed in Example 84, but with 0.78 g (5.1 mmol) of xylitol
instead of triglycerol. The compound was obtained having the
following properties:
[0565] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 12H), 1.00-1.70 (m, 22H), 2.00 (t, J=7.7 Hz, 2H),
3.50-4.25 (m, 9H), 5.32 (brs, 1H).
Example 86
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)mannitol
##STR00079##
[0567] The title compound was synthesized using the same procedure
as employed in Example 84, but with 0.93 g (5.1 mmol) of mannitol
instead of triglycerol.
Example 87
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)sorbitol
##STR00080##
[0569] The title compound was synthesized using the same procedure
as employed in Example 84, but with 0.93 g (5.1 mmol) of sorbitol
instead of triglycerol.
Example 88
Synthesis of
mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)dipentaerythritol
##STR00081##
[0571] The title compound was synthesized using the same procedure
as employed in Example 84, but with 1.3 g (5.1 mmol) of
dipentaerythritol instead of triglycerol.
Example 89
Synthesis of mono-O-(3,7,11,15-tetramethylhexadec-2-enyl)ascorbic
acid
##STR00082##
[0573] 0.90 g (6.7 mmol) of N-Chlorosuccinimide was suspended in
methylene chloride (8 mL). After addition of 0.52 mL (7.1 mmol) of
dimethylsulfide at 0.degree. C., the solution was stirred for 20
min. After addition of 1.0 g (3.4 mmol) of phytol, the mixture was
stirred for 1 hour at 0.degree. C., with additional stirring for 6
hours at room temperature. After addition of saturated sodium
bicarbonate aqueous solution, the reaction mixture was extracted
with methylene chloride. The extract was washed with saturated
brine, and dried over anhydrous sodium sulfate. After filtration,
the filtrate was concentrated to obtain
3,7,11,15-tetramethylhexadec-2-ene-1-chloride as a crude
product.
[0574] 0.52 mL (3.7 mmol) of triethylamine was added and dissolved
in a suspension of 0.60 g (3.4 mmol) of ascorbic acid in
acetonitrile (7 mL). After the above crude product of
3,7,11,15-tetramethylhexadec-2-ene-1-chloride was added at room
temperature, the reaction mixture was heated for 2 hours at
90.degree. C. The reaction solution was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 90
Synthesis of methyl 5,9,13-trimethyltetradec-4-enoate
##STR00083##
[0576] A mixture of 0.29 mL (3.9 mmol) of propionic acid and
trimethyl orthoacetate 1.0 mL (7.8 mmol) was slowly added dropwise
to a solution of 8.7 g (39 mmol) of tetrahydronerolidol and 11 mL
(86 mmol) of trimethyl orthoacetate at 140.degree. C. After the
reaction mixture was stirred for 18 hours at the same temperature,
a mixture of 0.10 mL (1.3 mmol) of propionic acid and 0.3 mL (2.3
mmol) of trimethyl orthoacetate was added with additional stirring
for 2 hours. The reaction mixture was subjected to simple
distillation (external temperature 140.degree. C., vacuum degree:
15 kPa) to release components with low boiling point, and the
resulting residue was purified by silica gel column chromatography
(ethyl acetate/hexane mixture) to obtain 7.0 g of the title
compound (65% yield) as a colorless transparent liquid. The results
of NMR analysis of the obtained compound are as shown below.
[0577] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 15H), 1.96 (td, J=7.1, 18.2 Hz,
2H), 2.25-2.35 (m, 4H), 3.67 (s, 3H), 5.08 (brs, 1H).
Example 91
Synthesis of 5,9,13-trimethyltetradec-4-en-1-ol
##STR00084##
[0579] Under a nitrogen atmosphere, 16.8 g (443 mmol) of lithium
aluminum hydride was added little by little at 0.degree. C. to a
solution of 50.0 g (177 mmol) of methyl
5,9,13-trimethyltetradec-4-enoate in dry tetrahydrofuran (440 mL).
After being stirred at 50.degree. C. for 4 hours, the reaction
mixture was cooled on ice, followed by careful addition of
saturated sodium sulfate aqueous solution until the resulting gray
suspension turned white. Sodium sulfate was added to the solution
at room temperature for drying. After filtration, the filtrate was
concentrated to obtain 45 g of the title compound (100% yield) as a
slightly yellow transparent liquid. The results of NMR analysis of
the obtained compound are as shown below.
[0580] .sup.1H-NMR spectrum (400 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 17H), 1.90-2.20 (m, 4H), 3.60-3.70
(m, 2H), 5.14 (t, J=7.1 Hz, 1H).
Example 92
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enoyl)glycerol
##STR00085##
[0582] 1.0 g (3.5 mmol) of methyl 5,9,13-trimethyltetradec-4-enoate
was slowly added dropwise to a solution of 0.65 g (7.1 mmol) of
glycerol and 0.59 g (4.3 mmol) of potassium carbonate in dry
N,N-dimethylformamide (3.5 mL) at 80.degree. C. After the reaction
mixture was stirred at 100.degree. C. for 18 hours, 1M hydrochloric
acid was added. The resulting solution was extracted with ether,
and the extract was washed with saturated sodium bicarbonate
aqueous solution and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated, and the resulting residue was purified by silica gel
column chromatography (ethyl acetate/hexane mixture) to obtain the
title compound.
[0583] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0584] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 15H), 1.97 (td, J=7.8, 17.0 Hz,
2H), 2.13 (t, J=6.1 Hz, 1H, OH), 2.25-2.45 (m, 4H), 2.55 (d, J=5.2
Hz, 1H, OH), 3.50-4.00 (m, 3H), 4.10-4.25 (m, 2H), 5.08 (t, J=6.7
Hz, 1H).
Example 93
Synthesis of
mono-O-(5,9,13-trimethyltetradec-4-enoyl)erythritol
##STR00086##
[0586] 1.0 g (3.5 mmol) of methyl 5,9,13-trimethyltetradec-4-enoate
was slowly added dropwise to a solution of erythritol 0.86 g (7.1
mmol) and 0.59 g (4.3 mmol) of potassium carbonate in dry
N,N-dimethylformamide (3.5 mL) at 80.degree. C. After the reaction
mixture was stirred at 100.degree. C. for 18 hours, 1M hydrochloric
acid was added. The resulting solution was extracted with ether,
and the extract was washed with saturated sodium bicarbonate
aqueous solution and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated, and the resulting residue was purified by silica gel
column chromatography (ethyl acetate/hexane mixture) to obtain 275
mg of the title compound (21% yield).
[0587] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0588] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.60 (m, 12H), 1.61 and 1.68 (s, 3H,
5-CH.sub.3), 1.97 (m, 2H), 2.18 (brs, 1H, OH), 2.30-2.45 (m, 4H),
2.69 (brs, 1H, OH), 2.84 (brs, 1H, OH), 3.63 (m, 1H), 3.80-3.95 (m,
3H), 4.25-4.40 (m, 2H), 5.08 (t, 1H).
Example 94
Synthesis of
mono-O-(5,9,13-trimethyltetradec-4-enoyl)pentaerythritol
##STR00087##
[0590] The title compound was synthesized using the same procedure
as employed in Example 92, but with 0.96 g (7.1 mmol) of
pentaerythritol instead of erythritol. The compound was obtained
(469 mg, 35% yield) having the following properties:
[0591] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.60 (m, 12H), 1.61 and 1.67 (s, 3H,
5-CH.sub.3), 1.97 (m, 2H), 2.30-2.45 (m, 4H), 2.54 (brs, 3H, OH),
3.64 (s, 6H), 4.23 (s, 2H), 5.07 (t, J=6.8 Hz, 1H).
Example 95
Synthesis of
mono-O-(5,9,13-trimethyltetradec-4-enoyl)diglycerol
##STR00088##
[0593] 1.0 g (3.5 mmol) of methyl 5,9,13-trimethyltetradec-4-enoate
was slowly added dropwise to a solution of 1.18 g (7.1 mmol) of
diglycerol and 0.59 g (4.3 mmol) of potassium carbonate in dry
N,N-dimethylformamide (3.5 mL) at 80.degree. C. After the reaction
mixture was stirred at 100.degree. C. for 18 hours, 1M hydrochloric
acid was added. The resulting solution was extracted with ethyl
acetate, and the extract was washed with saturated sodium
bicarbonate aqueous solution and saturated brine, successively, and
dried over anhydrous sodium sulfate. After filtration, the filtrate
was concentrated, and the resulting residue was purified by silica
gel column chromatography (methanol/methylene chloride mixture) to
obtain 249 mg of the title compound (17% yield).
[0594] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0595] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.60 (m, 12H), 1.61 and 1.68 (s, 3H,
5-CH.sub.3), 1.97 (m, 2H), 2.25-2.43 (m, 4H), 3.50-4.20 (m, 10H),
5.08 (t, J=6.8 Hz, 1H).
Example 96
Synthesis of
mono-O-(5,9,13-trimethyltetradec-4-enoyl)triglycerol
##STR00089##
[0597] The title compound was synthesized using the same procedure
as employed in Example 95, but with 1.7 g (7.1 mmol) of triglycerol
instead of diglycerol, having the following properties:
[0598] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.58 (m, 12H), 1.60 and 1.67 (s, 3H,
5-CH.sub.3), 1.96 (m, 2H), 2.25-2.40 (m, 4H), 3.50-3.80 (m, 11H),
3.89 (m, 1H), 4.00 (m, 1H), 4.10-4.20 (m, 2H), 5.08 (t, J=6.6 Hz,
1H).
Example 97
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enoyl)xylitol
##STR00090##
[0600] The title compound was synthesized using the same procedure
as employed in Example 95, but with 1.08 g (7.08 mmol) of xylitol
instead of diglycerol. The compound was obtained (306 mg, 22%
yield) having the following properties:
[0601] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.60 (m, 12H), 1.61 and 1.68 (s, 3H,
5-CH.sub.3), 1.97 (m, 2H), 2.25-2.45 (m, 4H), 3.66 (brs, 1H),
3.75-3.90 (m, 3H), 4.02 (m, 1H), 4.24 (d, J=5.8 Hz, 2H), 5.08 (t,
J=6.4 Hz, 1H).
Example 98
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enoyl)mannitol
##STR00091##
[0603] The title compound was synthesized using the same procedure
as employed in Example 95, but with 1.29 g (7.08 mmol) of mannitol
instead of diglycerol. The compound was obtained (367 mg, 24%
yield) having the following properties:
[0604] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3+3% CD.sub.3OD,
TMS) .delta.: 0.80-0.95 (m, 9H), 1.00-1.58 (m, 12H), 1.60 and 1.67
(s, 3H, 5-CH.sub.3), 1.96 (m, 2H), 2.25-2.45 (m, 4H), 3.65-3.95 (m,
6H), 4.24 (dd, 11.5 Hz, 1H), 4.39 (dd, J=2.9, 11.5 Hz, 1H), 5.08
(brs, 1H).
Example 99
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enoyl)sorbitol
##STR00092##
[0606] The title compound was synthesized using the same procedure
as employed in Example 95, but with 1.29 g (7.08 mmol) of sorbitol
instead of diglycerol. The compound was obtained (439 mg, 29%
yield) having the following properties:
[0607] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.58 (m, 12H), 1.59 and 1.66 (s, 3H,
5-CH.sub.3), 1.96 (m, 2H), 2.20-2.45 (m, 4H), 3.55-4.60 (m, 8H),
5.07 (brs, 1H).
Example 100
Synthesis of
mono-O-(5,9,13-trimethyltetradec-4-enoyl)dipentaerythritol
##STR00093##
[0609] The title compound was synthesized using the same procedure
as employed in Example 95, but with 1.80 g (7.08 mmol) of
dipentaerythritol instead of diglycerol. The compound was obtained
(224 mg, 13% yield) having the following properties:
[0610] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3+3% CD.sub.3OD,
TMS) .delta.: 0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.61 and 1.68
(s, 3H, 5-CH.sub.3), 1.99 (m, 2H), 2.25-2.45 (m, 4H), 3.35-3.60 (m,
14H), 4.07 (s, 2H), 5.07 (t, 0.1=6.8 Hz, 1H).
Example 101
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enoyl)ascorbic
acid
##STR00094##
[0612] 0.62 g (3.5 mmol) of ascorbic acid was dissolved in
concentrated sulfuric acid (16 mL). After addition of 1.0 g (3.5
mmol) of methyl 5,9,13-trimethyltetradec-4-enoate, the mixture was
stirred for 24 hours at room temperature. The reaction mixture was
poured into iced water, and extracted with ethyl acetate. The
extract was washed with water, 1M hydrochloric acid, saturated
sodium bicarbonate aqueous solution, and saturated brine,
successively, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated, and the resulting
residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 102
Synthesis of 1-O-(5,9,13-trimethyltetradec-4-enyl)-D-glucoside
##STR00095##
[0614] 4.0 g (10 mmol) of .beta.-D-glucose pentaacetate and 2.0 g
(7.9 mmol) of 5,9,13-trimethyltetradec-4-en-1-ol were dissolved in
dry acetonitrile (8 mL). 2.0 mL (16 mmol) of boron trifluoride
diethyl etherate complex was added to the solution with cooling on
ice. The reaction mixture was allowed to warm up slowly to room
temperature while being stirred for 24 hours before addition of 3.3
mL (24 mmol) of triethylamine at 0.degree. C. The resulting
solution was diluted with ethyl acetate, and washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over sodium sulfate.
After filtration, the filtrate was concentrated to obtain
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-glucopyranoside
tetraacetate as a crude product.
[0615] The above obtained crude product of
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-glucopyranoside
tetraacetate was dissolved in methanol/tetrahydrofuran (1:1, 8 mL),
and 0.79 mL (0.79 mmol) of 1M sodium methylate in methanol was
added at room temperature. After being stirred for 24 hours, 62
.mu.L (0.86 mmol) of acetyl chloride was added to the reaction
mixture and the mixture was confirmed to be weakly acidic. After
addition of water, the solution was extracted with ethyl acetate.
The extract was washed with saturated brine, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated, and the resulting residue was purified by silica gel
column chromatography (methanol/methylene chloride mixture) to
obtain 284 mg of the title compound (9% yield in 2 steps). The
results of NMR analysis of the obtained compound are as shown
below.
[0616] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.80 (in, 17H), 1.90-2.15 (m, 4H), 3.30 (d,
J=8.8 Hz, 1H), 3.39 (t, J=8.0 Hz, 1H), 3.45-3.70 (m, 3H), 3.80-3.93
(m, 3H), 4.30 (d, J=7.6 Hz, 1H), 5.09 (brs, 1H).
Example 103
Synthesis of
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-xylopyranoside
##STR00096##
[0618] The title compound was synthesized using the same procedure
as employed in Example 102, but with 3.25 g (10.2 mmol) of D-xylose
tetraacetate instead of .beta.-D-glucose pentaacetate. The compound
was obtained (420 mg, 13% yield in 2 steps) having the following
properties:
[0619] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.75 (m, 17H), 1.90-2.10 (m, 4H), 3.30-4.07
(m, 7H), 4.38 (d, J=6.0 Hz, 0.6H), 4.80 (d, J=3.7 Hz, 0.4H), 5.11
(brs, 1H).
Example 104
Synthesis of
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-galactoside
##STR00097##
[0621] The title compound was synthesized using the same procedure
as employed in Example 102, but with 4.0 g (10 mmol) of D-galactose
pentaacetate instead of .beta.-D-glucose pentaacetate. The compound
was obtained (383 mg, 12% yield in 2 steps) having the following
properties:
[0622] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 17H), 1.90-2.05 (m, 4H), 3.40-4.12
(m, 8H), 4.24 (d, J=6.7 Hz, 1H), 5.10 (brs, 1H).
Example 105
Synthesis of 1-O-(5,9,13-trimethyltetradec-4-enyl)-D-mannoside
##STR00098##
[0624] The title compound was synthesized using the same procedure
as employed in Example 102, but with 4.0 g (10 mmol) of D-mannose
pentaacetate instead of .beta.-D-glucose pentaacetate. The compound
was obtained (222 mg, 7% yield in 2 steps) having the following
properties:
[0625] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 17H), 1.85-2.10 (m, 4H), 3.32-4.07
(m, 7H), 3.38 (m, 1H), 3.51 (d, J=9.8 Hz, 1H), 3.63 (m, 1H),
3.70-4.05 (m, 5H), 4.81 (s, 1H), 5.05 (brs, 1H).
Example 106
Synthesis of 1-O-(5,9,13-trimethyltetradec-4-enyl)-D-maltoside
##STR00099##
[0627] 6.93 g (10.2 mmol) of D-Maltose octaacetate and 2.0 g (7.9
mmol) of 5,9,13-trimethyltetradec-4-en-1-ol were dissolved in dry
acetonitrile (8 mL). 2.0 mL (16 mmol) of boron trifluoride diethyl
etherate complex was added to the solution with cooling on ice. The
reaction mixture was allowed to warm up slowly to room temperature
while being stirred for 24 hours before addition of 3.3 mL (24
mmol) of triethylamine at 0.degree. C. The resulting solution was
diluted with ethyl acetate, and washed with water, 1M hydrochloric
acid, saturated sodium bicarbonate aqueous solution, and saturated
brine, successively, and dried over sodium sulfate. After
filtration, the filtrate was concentrated to obtain
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-maltoside heptaacetate as a
crude product.
[0628] The above obtained crude product of
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-maltoside heptaacetate was
dissolved in methanol/tetrahydrofuran (1:1, 8 mL), and 0.79 mL
(0.79 mmol) of 1M sodium methylate in methanol was added at room
temperature. After being stirred for 24 hours, 62 .mu.L (0.86 mmol)
of acetyl chloride was added to the reaction mixture and the
mixture was confirmed to be weakly acidic. The mixture was
concentrated, and the resulting residue was purified by silica gel
column chromatography (methanol/methylene chloride mixture) to
obtain 338 mg of the title compound (7% yield in 2 steps). The
results of NMR analysis of the obtained compound are as shown
below.
[0629] .sup.1H-NMR spectrum (300 MHz, CD.sub.3OD, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 17H), 1.90-2.10 (m, 4H), 3.10-3.95
(m, 14H), 4.24 (d, J=7.7 Hz, 1H), 4.60 (s, 2H), 5.13 (brs, 1H).
Example 107
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enyl)glycerol
##STR00100##
[0631] 0.82 mL (5.9 mmol) of triethylamine, 0.90 g (4.7 mmol) of
p-toluenesulfonyl chloride and 38 mg (0.39 mmol) of trimethylamine
hydrochloride were added to a solution of 1.0 g (3.9 mmol) of
5,9,13-trimethyltetradec-4-en-1-ol in dry methylene chloride (3 mL)
at 0.degree. C., sequentially. After being stirred for 1 hour at
room temperature, 0.12 mL (1.0 mmol) of
N,N-dimethyl-1,3-propanediamine was added to the reaction mixture.
After being stirred for 30 min, the mixture was diluted with ethyl
acetate. The solution was washed with water, 1M hydrochloric acid,
saturated sodium bicarbonate aqueous solution, and saturated brine,
successively, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated to obtain
(5,9,13-trimethyltetradec-4-enyl)tosylate as a crude product.
[0632] 0.26 g (55%, 5.9 mmol) of sodium hydride was added to a
solution of 0.54 g (5.9 mmol) of glycerol in dry
N,N-dimethylformamide (6 mL) with cooling on ice. After the mixture
was stirred for 30 min at 50.degree. C., the above
(5,9,13-trimethyltetradec-4-enyl)tosylate was added dropwise, with
additional stirring for 18 hours at the same temperature. After
addition of water at 0.degree. C., the reaction mixture was
extracted with ethyl acetate. The extract was washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(ethyl acetate/hexane mixture) to obtain 73 mg of the title
compound (6% yield in 2 steps). The results of NMR analysis of the
obtained compound are as shown below.
[0633] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 9H), 1.00-1.70 (m, 17H), 1.90-2.10 (m, 4H), 3.40-3.60
(m, 4H), 3.61-3.90 (m, 3H), 5.10 (brt, J=6.0 Hz, 1H).
Example 108
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enyl)erythritol
##STR00101##
[0635] The title compound was synthesized using the same procedure
as employed in Example 107, but with 0.72 g (5.9 mmol) of
erythritol instead of glycerol. The compound was obtained (64 mg,
5% yield in 2 steps) having the following properties:
[0636] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 9H), 1.00-1.70 (m, 17H), 1.90-2.10 (m, 4H), 2.29 (brs,
OH), 2.64 (brs, OH), 2.75 (brs, OH), 3.49 (t, J=6.4 Hz, 2H), 3.59
(t, J=5.5 Hz, 2H), 3.65-3.90 (m, 4H), 5.09 (t, J=6.9 Hz, 1H).
Example 109
Synthesis of
mono-O-(5,9,13-trimethyltetradec-4-enyl)pentaerythritol
##STR00102##
[0638] The title compound was synthesized using the same procedure
as employed in Example 107, but with 0.80 g (5.9 mmol) of
pentaerythritol instead of glycerol. The compound was obtained (375
mg, 26% yield in 2 steps) having the following properties:
[0639] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 9H), 1.00-1.70 (m, 17H), 1.90-2.10 (m, 4H), 2.59 (brs,
30H), 3.42 (t, J=6.4 Hz, 2H), 3.47 (s, 2H), 3.73 (d, J=4.5 Hz, 6H),
5.09 (t, J=7.0 Hz, 1H).
Example 110
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enyl)diglycerol
##STR00103##
[0641] 0.82 mL (5.9 mmol) of triethylamine, 0.90 g (4.7 mmol) of
p-toluenesulfonyl chloride, and 38 mg (0.39 mmol) of trimethylamine
hydrochloride were added to a solution of
5,9,13-trimethyltetradec-4-en-1-ol 1.0 g (3.9 mmol) in dry
methylene chloride (3 mL) at 0.degree. C., sequentially. After
being stirred for 1 hour at room temperature, 0.12 mL (1.0 mmol) of
N,N-dimethyl-1,3-propanediamine was added to the reaction mixture
at 0.degree. C. After being stirred for 30 min, the mixture was
diluted with ethyl acetate. The solution was washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated to obtain
(5,9,13-trimethyltetradec-4-enyl)tosylate as a crude product.
[0642] 0.26 g (55%, 5.9 mmol) of sodium hydride was added to a
solution of 0.98 g (5.9 mmol) of diglycerol in dry
N,N-dimethylformamide (6 mL) with cooling on ice. After the mixture
was stirred for 30 min at 50.degree. C., the above
(5,9,13-trimethyltetradec-4-enyl)tosylate was added dropwise, with
additional stirring for 18 hours at the same temperature. After
addition of water at 0.degree. C., the reaction mixture was
extracted with ethyl acetate. The extract was washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain 535 mg of the title
compound (34% yield in 2 steps). The results of NMR analysis of the
obtained compound are as shown below.
[0643] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 9H), 1.00-1.70 (m, 17H), 1.90-2.10 (m, 4H), 3.40-4.00
(m, 12H), 5.10 (t, J=7.1 Hz, 1H).
Example 111
Synthesis of
mono-O-(5,9,13-trimethyltetradec-4-enyl)triglycerol
##STR00104##
[0645] The title compound was synthesized using the same procedure
as employed in Example 110, but with 1.42 g (5.9 mmol) of
triglycerol instead of diglycerol. The compound was obtained (549
mg, 29% yield in 2 steps) having the following properties:
[0646] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 9H), 1.00-1.68 (m, 14H), 1.58 and 1.67 (s, 3H,
5-CH.sub.3), 1.90-2.10 (m, 4H), 3.40-4.00 (m, 17H), 5.09 (t, J=6.8
Hz, 1H).
Example 112
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enyl)xylitol
##STR00105##
[0648] The title compound was synthesized using the same procedure
as employed in Example 110, but with 0.90 g (5.9 mmol) of xylitol
instead of diglycerol, having the following properties:
[0649] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 9H), 1.00-1.70 (m, 17H), 1.90-2.10 (m, 4H), 3.40-4.00
(m, 9H), 5.10 (t, J=6.4 Hz, 1H).
Example 113
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enyl)mannitol
##STR00106##
[0651] The title compound was synthesized using the same procedure
as employed in Example 110, but with of mannitol instead of
diglycerol. The compound was obtained (241 mg, 15% yield in 2
steps) having the following properties:
[0652] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 9H), 1.00-1.70 (m, 14H), 1.57 and 1.66 (s, 3H,
5-CH.sub.3), 1.85-2.10 (m, 4H), 3.40-3.95 (m, 10H), 5.07 (brs,
1H).
Example 114
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enyl)sorbitol
##STR00107##
[0654] The title compound was synthesized using the same procedure
as employed in Example 110, but with 1.07 g (5.9 mmol) of sorbitol
instead of diglycerol. The compound was obtained (216 mg, 13% yield
in 2 steps) having the following properties:
[0655] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.8-0.9 (m, 9H), 1.00-1.70 (m, 14H), 1.58 and 1.67 (s, 3H,
5-CH.sub.3), 1.85-2.10 (m, 4H), 3.40-4.00 (m, 10H), 5.09 (brs,
1H).
Example 115
Synthesis of
mono-O-(5,9,13-trimethyltetradec-4-enyl)dipentaerythritol
##STR00108##
[0657] The title compound was synthesized using the same procedure
as employed in Example 110, but with 1.5 g (5.9 mmol) of
dipentaerythritol instead of diglycerol. The compound was obtained
(245 mg, 13% yield in 2 steps) having the following properties:
[0658] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3+3% CD.sub.3OD,
TMS) .delta.: 0.8-0.9 (m, 9H), 1.00-1.65 (m, 14H), 1.58 and 1.67
(s, 3H, 5-CH.sub.3), 1.90-2.05 (m, 4H), 3.35-3.49 (m, 8H),
3.52-3.65 (m, 10H), 5.09 (t, J=7.2 Hz, 1H).
Example 116
Synthesis of mono-O-(5,9,13-trimethyltetradec-4-enyl)ascorbic
acid
##STR00109##
[0660] 0.82 mL (5.9 mmol) of triethylamine, 0.90 g (4.7 mmol) of
p-toluenesulfonyl chloride, 38 mg (0.39 mmol) of trimethylamine
hydrochloride was added to a solution of 1.0 g (3.9 mmol) of
5,9,13-timethyltetradec-4-en-1-ol in dry methylene chloride (3 mL)
at 0.degree. C., sequentially. After being stirred for 1 hour at
room temperature, 0.12 mL (1.0 mmol) of
N,N-dimethyl-1,3-propanediamine was added to the reaction mixture
at 0.degree. C. After being stirred for 30 min, the mixture was
diluted with ethyl acetate. The resulting solution was washed with
water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous
solution, and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated to obtain (5,9,13-trimethyltetradec-4-enyl)tosylate as
a crude product. 0.60 mL (4.3 mmol) of triethylamine was added and
dissolved in a suspension of 0.69 g (3.9 mmol) of ascorbic acid in
acetonitrile (8 mL). The above crude product of
(5,9,13-trimethyltetradec-4-enyl)tosylate was added thereto at room
temperature, and the reaction mixture was heated for 2 hours at
90.degree. C. The reaction mixture was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 117
Synthesis of 3,7,11-trimethyldodec-2-ene-1-nitrile
##STR00110##
[0662] 82.3 g (617 mmol) of N-Chlorosuccinimide was suspended in
methylene chloride (750 mL). After addition of 48 mL (0.65 mol) of
dimethylsulfide at 0.degree. C., the solution was stirred for 20
min. After addition of 69.8 g (0.308 mol) of tetrahydrofarnesol,
the mixture was stirred for 1 hour at 0.degree. C., with additional
stirring for 1 hour at room temperature. After addition of
saturated sodium bicarbonate aqueous solution, the reaction mixture
was extracted with methylene chloride. The extract was washed with
saturated brine, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated to obtain
3,7,11-trimethyldodec-2-ene-1-chloride as a crude product.
[0663] 18.1 g (0.370 mol) of sodium cyanide was added to a solution
of the above crude product of
3,7,11-trimethyldodec-2-ene-1-chloride in N,N-dimethylformamide
(500 mL). The solution was stirred for 10 hours at room
temperature. After addition of water at 0.degree. C., the reaction
mixture was extracted with ether. The extract was washed with
saturated sodium bicarbonate aqueous solution and saturated brine,
successively, and dried over sodium sulfate. After filtration, the
filtrate was concentrated, and the resulting residue was purified
by silica gel column chromatography (ethyl acetate/hexane mixture)
to obtain 67.2 g of the title compound (93% yield in 2 steps) as a
yellow liquid. The results of NMR analysis of the obtained compound
are as shown below.
[0664] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.75 (m, 12H), 1.66 and 1.74 (s, 3H,
3-CH.sub.3), 2.00 (t, J=7.7 Hz, 2H), 3.04 (d, J=7.0 Hz, 2H), 5.16
(t, J=7.0 Hz, 1H).
Example 118
Synthesis of methyl 4,8,12-trimethyltridec-3-enoate
##STR00111##
[0666] Water (130 mL) and 40 g (0.71 mol) of potassium hydroxide
was added to a solution of 67.2 g (285 mmol) of
3,7,11-trimethyldodec-2-ene-1-nitrile in ethanol (470 mL). The
solution was stirred for 18 hours at 80.degree. C. After the
reaction mixture was concentrated, and then neutralized with
concentrated hydrochloric acid, and extracted with ethyl acetate.
The extract was washed with saturated sodium bicarbonate aqueous
solution and saturated brine, successively, and dried over sodium
sulfate. After filtration, the filtrate was concentrated to obtain
4,8,12-trimethyltridec-3-enoic acid as a crude product.
[0667] The above obtained crude product of
4,8,12-trimethyltridec-3-enoic acid was dissolved in methanol (350
mL). Concentrated sulfuric acid (7 mL) was added thereto and
stirred for 18 hours at room temperature. Sodium bicarbonate was
slowly added to the reaction mixture and the mixture was confirmed
to be neutralized. After filtration, the filtrate was concentrated,
and diluted with ethyl acetate. The solution was washed with water
and saturated brine, successively, and dried over anhydrous
magnesium sulfate. After filtration, the filtrate was concentrated,
and the resulting residue was purified by silica gel column
chromatography (ethyl acetate/hexane mixture) to obtain 58.8 g of
the title compound (77% yield in 2 steps) as a slightly yellow
liquid. The results of NMR analysis of the obtained compound are as
shown below.
[0668] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.58 (m, 12H), 1.62 and 1.73 (s, 3H,
4-CH.sub.3), 1.99 (t, J=7.7 Hz, 2H), 3.05 (d, J=7.1 Hz, 2H), 3.68
(s, 3H), 5.31 (t, J=7.1 Hz, 1H).
Example 119
Synthesis of 4,8,12-trimethyltridec-3-en-1-ol
##STR00112##
[0670] Under a nitrogen atmosphere, 12.4 g (0.326 mol) of lithium
aluminum hydride was added little by little to a solution of 35 g
(0.13 mol) of methyl 4,8,12-trimethyltridec-3-enoate in dry
tetrahydrofuran (320 mL) at 0.degree. C. After being stirred at
50.degree. C. for 2 hours, the reaction mixture was cooled on ice,
followed by careful addition of saturated sodium sulfate aqueous
solution until the resulting gray suspension turned white. Sodium
sulfate was added to the solution at room temperature for drying.
After filtration, the filtrate was concentrated to obtain 31 g of
the title compound (99% yield) as a colorless transparent liquid.
The results of NMR analysis of the obtained compound are as shown
below.
[0671] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.63 and 1.72 (s, 3H,
4-CH.sub.3), 1.94-2.07 (m, 2H), 2.29 (m, 2H), 3.63 (m, 2H), 5.12
(t, J=7.1 Hz, 1H).
Example 120
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enoyl)glycerol
##STR00113##
[0673] 1.0 g (3.7 mmol) of methyl 4,8,12-trimethyltridec-3-enoate
was slowly added dropwise to a solution of 0.86 g (9.3 mmol) of
glycerol and 0.62 g (4.4 mmol) of potassium carbonate in dry
N,N-dimethylformamide (4 mL) at 100.degree. C. After the reaction
mixture was stirred at 100.degree. C. for 18 hours, 1M hydrochloric
acid was added. The resulting solution was extracted with ether,
and the extract was washed with saturated sodium bicarbonate
aqueous solution and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated, and the resulting residue was purified by silica gel
column chromatography (ethyl acetate/hexane mixture) to obtain 287
mg of the title compound (24% yield) as a colorless viscous
liquid.
[0674] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0675] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.63 and 1.74 (s, 3H,
4-CH.sub.3), 2.00 (t, J=7.2 Hz, 2H), 3.10 (d, J=7.1 Hz, 2H),
3.55-4.00 (m, 3H), 4.10-4.30 (m, 2H), 5.30 (t, J=7.1 Hz, 1H).
Example 121
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enoyl)erythritol
##STR00114##
[0677] The title compound was synthesized using the same procedure
as employed in Example 120, but with 1.14 g (9.31 mmol) of
erythritol instead of glycerol. The compound was obtained (246 mg,
19% yield) having the following properties:
[0678] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.63 and 1.74 (s, 3H,
4-CH.sub.3), 2.00 (t, J=7.2 Hz, 2H), 3.11 (d, J=7.1 Hz, 2H),
3.60-3.95 (m, 4H), 4.25-4.40 (m, 2H), 5.30 (t, J=7.1 Hz, 1H).
Example 122
Synthesis of
mono-O-(4,8,12-trimethyltridec-3-enoyl)pentaerythritol
##STR00115##
[0680] The title compound was synthesized using the same procedure
as employed in Example 120, but with 1.27 g (9.31 mmol) of
pentaerythritol instead of glycerol. The compound was obtained (196
mg, 15% yield) having the following properties:
[0681] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.64 and 1.74 (s, 3H,
4-CH.sub.3), 2.00 (t, J=7.6 Hz, 2H), 2.52 (brt, J=5.4 Hz, 3H, OH),
3.10 (d, J=7.2 Hz, 2H), 3.65 (d, J=5.4 Hz, 6H), 4.23 (s, 2H), 5.29
(t, J=7.2 Hz, 1H).
Example 123
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enoyl)diglycerol
##STR00116##
[0683] 1.0 g (3.7 mmol) of methyl 4,8,12-trimethyltridec-3-enoate
was slowly added dropwise to a solution of 1.55 g (9.31 mmol) of
diglycerol and 0.62 g (4.5 mmol) of potassium carbonate in dry
N,N-dimethylformamide (4 mL) at 80.degree. C. After the reaction
mixture was stirred at 100.degree. C. for 18 hours, 1M hydrochloric
acid was added. The resulting extract was extracted with ethyl
acetate, and the extract was washed with saturated sodium
bicarbonate aqueous solution and saturated brine, successively, and
dried over anhydrous sodium sulfate. After filtration, the filtrate
was concentrated, and the resulting residue was purified by silica
gel column chromatography (methanol/methylene chloride mixture) to
obtain 163 mg of the title compound (11% yield).
[0684] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0685] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.62 and 1.73 (s, 3H,
4-CH.sub.3), 1.99 (t, J=7.7 Hz, 2H), 3.09 (d, J=6.8 Hz, 2H),
3.50-4.30 (m, 10H), 5.30 (t, J=6.8 Hz, 1H).
Example 124
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enoyl)triglycerol
##STR00117##
[0687] The title compound was synthesized using the same procedure
as employed in Example 123, but with 2.24 g (9.31 mmol) of
triglycerol instead of diglycerol. The compound was obtained (148
mg, 8% yield) having the following properties:
[0688] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.62 and 1.73 (s, 3H,
4-CH.sub.3), 1.99 (t, J=7.1 Hz, 2H), 3.09 (d, J=7.1 Hz, 2H),
3.50-4.25 (m, 15H), 5.30 (t, J=7.1 Hz, 1H).
Example 125
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enoyl)xylitol
##STR00118##
[0690] The title compound was synthesized using the same procedure
as employed in Example 123, but with 1.42 g (9.31 mmol) of xylitol
instead of diglycerol. The compound was obtained (284 mg, 20%
yield) having the following properties:
[0691] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.75 (m, 15H), 1.99 (t, J=6.6 Hz, 2H), 3.09
(d, J=7.1 Hz, 2H), 3.60-4.20 (m, 5H), 4.25 (d, J=5.7 Hz, 2H), 5.29
(t, J=7.1 Hz, 1H).
Example 126
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enoyl)mannitol
##STR00119##
[0693] The title compound was synthesized using the same procedure
as employed in Example 123, but with 1.7 g (9.3 mmol) of mannitol
instead of diglycerol. The compound was obtained (318 mg, 21%
yield) having the following properties:
[0694] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.61 and 1.72 (s, 3H,
4-CH.sub.3), 1.98 (t, J=7.1 Hz, 2H), 3.10 (brt, 2H), 3.60-4.40 (m,
8H), 5.29 (brs, 1H).
Example 127
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enoyl)sorbitol
##STR00120##
[0696] The title compound was synthesized using the same procedure
as employed in Example 123, but with 1.7 g (9.3 mmol) of sorbitol
instead of diglycerol. The compound was obtained (403 mg, 26%
yield) having the following properties:
[0697] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.62 and 1.73 (s, 3H,
4-CH.sub.3), 2.00 (t, J=7.5 Hz, 2H), 3.11 (d, J=6.8 Hz, 2H),
3.65-3.95 (m, 6H), 4.25 (dd, J=6.2, 11.6 Hz, 1H), 4.40 (dd, J=2.9,
11.6 Hz, 1H), 5.31 (t, J=6.8 Hz, 1H).
Example 128
Synthesis of
mono-O-(4,8,12-trimethyltridec-3-enoyl)dipentaerythritol
##STR00121##
[0699] The title compound was synthesized using the same procedure
as employed in Example 123, but with 2.37 g (9.31 mmol) of
dipentaerythritol instead of diglycerol. The compound was obtained
(225 mg, 13% yield) having the following properties:
[0700] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 15H), 2.00 (t, J=7.7 Hz, 2H), 3.08
(d, J=7.1 Hz, 2H), 3.38 (s, 2H), 3.42 (s, 2H), 3.55 (s, 4H), 3.59
(s, 6H), 4.08 (s, 2H), 5.28 (t, J=7.1 Hz, 1H).
Example 129
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enoyl)ascorbic
acid
##STR00122##
[0702] 0.65 g (3.7 mmol) of ascorbic acid was dissolved in
concentrated sulfuric acid (18 mL). After addition of 1.0 g (3.7
mmol) of methyl 4,8,12-trimethyltridec-3-enoate, the mixture was
stirred for 24 hours at room temperature. The reaction mixture was
poured into iced water, and extracted with ethyl acetate. The
extract was washed with water, 1M hydrochloric acid, saturated
sodium bicarbonate aqueous solution, and saturated brine,
successively, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated, and the resulting
residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 130
Synthesis of 1-O-(4,8,12-trimethyltridec-3-enyl)-D-glucoside
##STR00123##
[0704] 2.11 g (5.41 mmol) of .beta.-D-glucose pentaacetate and 1.0
g (4.2 mmol) of 4,8,12-trimethyltridec-3-en-1-ol were dissolved in
dry acetonitrile (4 mL). 1.0 mL (8.3 mmol) of boron trifluoride
diethyl etherate complex was added to the solution with cooling on
ice. The reaction mixture was allowed to warm up slowly to room
temperature while being stirred for 24 hours before addition of 1.7
mL (12 mmol) of triethylamine at 0.degree. C. The resulting
solution was diluted with ethyl acetate, and washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over sodium sulfate.
After filtration, the filtrate was concentrated to obtain
1-O-(4,8,12-trimethyltridec-3-enyl)-D-glucopyranoside tetraacetate
as a crude product.
[0705] The above obtained crude product of
1-O-(4,8,12-trimethyltridec-3-enyl)-D-glucopyranoside tetraacetate
was dissolved in methanol/tetrahydrofuran (1:1, 6 mL), and 0.42 mL
(0.42 mmol) of 1M sodium methylate in methanol was added at room
temperature. After being stirred for 24 hours, 30 .mu.L (0.42 mmol)
of acetyl chloride was added to the reaction mixture and confirmed
to be neutralized. After addition of water, the solution was
extracted with ethyl acetate. The extract was washed with saturated
brine, and dried over anhydrous sodium sulfate. After filtration,
the filtrate was concentrated, and the resulting residue was
purified by silica gel column chromatography (methanol/methylene
chloride mixture) to obtain the title compound. The results of NMR
analysis of the obtained compound are as shown below.
[0706] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.80 (m, 15H), 1.90-2.10 (m, 4H), 3.25-3.90
(m, 8H), 4.31 (brs, 1H), 5.12 (brs, 1H).
Example 131
Synthesis of
1-O-(4,8,12-trimethyltridec-3-enyl)-D-xylopyranoside
##STR00124##
[0708] The title compound was synthesized using the same procedure
as employed in Example 130, but with 1.72 g (5.41 mmol) of D-xylose
tetraacetate instead of .beta.-D-glucose pentaacetate, having the
following properties:
[0709] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.80 (m, 15H), 1.90-2.10 (m, 4H), 3.30-4.10
(m, 7H), 4.35 (d, J=5.8 Hz, 0.7H), 4.80 (brs, 0.3H), 5.10 (brs,
1H).
Example 132
Synthesis of 1-O-(4,8,12-trimethyltridec-3-enyl)-D-galactoside
##STR00125##
[0711] The title compound was synthesized using the same procedure
as employed in Example 130, but with 2.11 g (5.41 mmol) of
D-galactose pentaacetate instead of .beta.-D-glucose pentaacetate,
having the following properties:
[0712] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.80 (m, 15H), 1.85-2.10 (m, 4H), 3.40-4.10
(m, 8H), 4.26 (brs, 1H), 5.00-5.10 (m, 1H).
Example 133
Synthesis of 1-O-(4,8,12-trimethyltridec-3-enyl)-D-mannoside
##STR00126##
[0714] The title compound was synthesized using the same procedure
as employed in Example 130, but with 2.11 g (5.41 mmol) of
D-mannose pentaacetate instead of .beta.-D-glucose pentaacetate,
having the following properties:
[0715] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 15H), 1.90-2.10 (m, 4H), 3.30-3.65
(m, 3H), 3.73 (d, J=11.7 Hz, 1H), 3.80-4.10 (m, 3H), 4.81 (d, J=5.3
Hz, 1H), 5.10 (brs, 1H).
Example 134
Synthesis of 1-O-(4,8,12-trimethyltridec-3-enyl)-D-maltoside
##STR00127##
[0717] 3.67 g (5.41 mmol) of D-mannose octaacetate and 1.0 g (4.2
mmol) of 4,8,12-trimethyltridec-3-en-1-ol were dissolved in dry
acetonitrile (4 mL). 1.0 mL (8.0 mmol) of boron trifluoride diethyl
etherate complex was added to the solution with cooling on ice. The
reaction mixture was allowed to warm up slowly to room temperature
while being stirred for 24 hours before addition of 1.7 mL (12
mmol) of triethylamine at 0.degree. C. The resulting solution was
diluted with ethyl acetate, and washed with water, 1M hydrochloric
acid, saturated sodium bicarbonate aqueous solution, and saturated
brine, successively, and dried over sodium sulfate. After
filtration, the filtrate was concentrated to obtain
1-O-(4,8,12-trimethyltridec-3-enyl)-D-maltoside heptaacetate as a
crude product.
[0718] The above obtained crude product of
1-O-(4,8,12-trimethyltridec-3-enyl)-D-maltoside heptaacetate was
dissolved in methanol/tetrahydrofuran (1:1, 6 mL), and 0.42 mL
(0.42 mmol) of 1M sodium methylate in methanol was added at room
temperature. After being stirred for 24 hours, 30 .mu.L (0.42 mmol)
of acetyl chloride was added to the reaction mixture and the
mixture was confirmed to be neutralized. The resulting mixture was
concentrated, and the resulting residue was purified by silica gel
column chromatography (methanol/methylene chloride mixture) to
obtain the title compound. The results of NMR analysis of the
obtained compound are as shown below.
[0719] .sup.1H-NMR spectrum (300 MHz, CD.sub.3OD, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.80 (m, 15H), 1.85-2.10 (m, 4H), 3.15-3.90
(m, 14H), 4.20-4.30 (m, 1H), 4.59 (s, 1H), 5.13 (brs, 2H).
Example 135
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enyl)glycerol
##STR00128##
[0721] 0.63 mL (4.6 mmol) of triethylamine, 0.87 g (4.6 mmol) of
p-toluenesulfonyl chloride, and 20 mg (0.21 mmol) of trimethylamine
hydrochloride were added to a solution of 1.0 g (4.2 mmol) of
4,8,12-trimethyltridec-3-en-1-ol in dry methylene chloride (3 mL)
at 0.degree. C., sequentially. After being stirred for 2 hours at
room temperature, 0.10 mL (0.83 mmol) of
N,N-dimethyl-1,3-propanediamine was added to the reaction mixture
at 0.degree. C. After being stirred for 30 min, the mixture was
diluted with ethyl acetate. The resulting solution was washed with
water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous
solution, and saturated brine, successively, and then dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated to obtain (4,8,12-trimethyltridec-3-enyl)tosylate as a
crude product.
[0722] 0.27 g (55%, 6.2 mmol) of sodium hydride was added to a
solution of glycerol 0.57 g (6.2 mmol) in dry N,N-dimethylformamide
(6 mL) with cooling on ice. After the mixture was stirred for 30
min at 50.degree. C., the above
(4,8,12-trimethyltridec-3-enyl)tosylate was added dropwise, with
additional stirring for 10 hours at the same temperature. After
addition of water at 0.degree. C., the reaction mixture was
extracted with ethyl acetate. The extract was washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(ethyl acetate/hexane mixture) to obtain 79 mg of the title
compound (6% yield in 2 steps). The results of NMR analysis of the
obtained compound are as shown below.
[0723] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 15H), 1.90-2.05 (m, 2H), 2.15 (t,
J=5.3 Hz, 1H, OH), 2.25-2.35 (m, 2H), 2.61 (d, J=5.2 Hz, 1H, OH),
3.40-3.90 (m, 7H), 5.10 (t, J=7.7 Hz, 1H).
Example 136
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enyl)erythritol
##STR00129##
[0725] The title compound was synthesized using the same procedure
as employed in Example 135, but with 0.76 g (6.2 mmol) of
erythritol instead of glycerol, having the following
properties:
[0726] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 15H), 1.90-2.00 (m, 2H), 2.20-2.35
(m, 2H), 3.40-3.85 (m, 8H), 5.10 (brs, 1H).
Example 137
Synthesis of
mono-O-(4,8,12-trimethyltridec-3-enyl)pentaerythritol
##STR00130##
[0728] The title compound was synthesized using the same procedure
as employed in Example 135, but with 0.85 g (6.2 mmol) of
pentaerythritol instead of glycerol. The compound was obtained (191
mg, 13% yield in 2 steps) having the following properties:
[0729] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 15H), 1.90-2.05 (m, 2H), 2.20-2.35
(m, 2H), 2.52 (t, J=5.6 Hz, 3H, OH), 3.38-3.48 (m, 2H), 3.49 (s,
2H), 3.71 (d, J=5.6 Hz, 6H), 5.09 (t, J=6.8 Hz, 1H).
Example 138
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enyl)diglycerol
##STR00131##
[0731] 0.63 mL (4.6 mmol) of triethylamine, 0.87 g (4.6 mmol) of
p-toluenesulfonyl chloride, 20 mg (0.21 mmol) of trimethylamine
hydrochloride were added to a solution of 1.0 g (4.2 mmol) of
4,8,12-trimethyltridec-3-en-1-ol in dry methylene chloride (3 mL)
at 0.degree. C., sequentially. After being stirred for 2 hours at
room temperature, N,N-dimethyl-1,3-propanediamine was added to the
reaction mixture at 0.degree. C. After being stirred for 30 min,
the mixture was diluted with ethyl acetate. The resulting solution
was washed with water, 1M hydrochloric acid, saturated sodium
bicarbonate aqueous solution, and saturated brine, successively,
and dried over anhydrous sodium sulfate. After filtration, the
filtrate was concentrated to obtain
(4,8,12-trimethyltridec-3-enyl)tosylate as a crude product.
[0732] 0.27 g (55%, 6.2 mmol) of sodium hydride was added to a
solution of 1.04 g (6.2 mmol) of diglycerol in dry
N,N-dimethylformamide (6 mL) with cooling on ice. After the mixture
was stirred for 30 min at 50.degree. C., the above
(4,8,12-trimethyltridec-3-enyl)tosylate was added dropwise with
additional stirring for 18 hours at the same temperature. After
addition of water at 0.degree. C., the reaction mixture was
extracted with ethyl acetate. The extract was washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain 351 mg of the title
compound (22% yield in 2 steps). The results of NMR analysis of the
obtained compound are as shown below.
[0733] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (in, 15H), 1.90-2.05 (in, 2H),
2.20-2.35 (in, 2H), 3.40-4.00 (m, 12H), 5.10 (brs, 1H).
Example 139
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enyl)triglycerol
##STR00132##
[0735] The title compound was synthesized using the same procedure
as employed in Example 138, but with 1.5 g (6.2 mmol) of
triglycerol instead of diglycerol, having the following
properties:
[0736] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.61 and 1.69 (s, 3H,
4-CH.sub.3), 1.90-2.05 (m, 2H), 2.25-2.35 (m, 2H), 3.40-4.00 (m,
17H), 5.10 (brs, 1H).
Example 140
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enyl)xylitol
##STR00133##
[0738] The title compound was synthesized using the same procedure
as employed in Example 138, but with 0.95 g (6.2 mmol) of xylitol
instead of diglycerol, having the following properties:
[0739] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.70 (m, 15H), 1.90-2.05 (m, 2H), 2.20-2.35
(m, 2H), 3.40-4.00 (m, 9H), 5.10 (brs, 1H).
Example 141
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enyl)mannitol
##STR00134##
[0741] The title compound was synthesized using the same procedure
as employed in Example 138, but with 1.14 g (6.24 mmol) of mannitol
instead of diglycerol. The compound was obtained (135 mg, 8% yield
in 2 steps) having the following properties:
[0742] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.63 (m, 12H), 1.60 and 1.68 (s, 3H,
4-CH.sub.3), 1.85-2.05 (m, 2H), 2.20-2.35 (m, 2H), 3.40-3.95 (m,
10H), 5.07 (brs, 1H).
Example 142
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enyl)sorbitol
##STR00135##
[0744] The title compound was synthesized using the same procedure
as employed in Example 138, but with 1.14 g (6.24 mmol) of sorbitol
instead of diglycerol. The compound was obtained (103 mg, 6% yield
in 2 steps) having the following properties:
[0745] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.58 (m, 12H), 1.60 and 1.68 (s, 3H,
4-CH.sub.3), 1.90-2.03 (m, 2H), 2.20-2.35 (m, 2H), 3.40-4.00 (m,
10H), 5.08 (brs, 1H).
Example 143
Synthesis of
mono-O-(4,8,12-trimethyltridec-3-enyl)dipentaerythritol
##STR00136##
[0747] The title compound was synthesized using the same procedure
as employed in Example 138, but with 1.59 g (6.24 mmol) of
dipentaerythritol instead of diglycerol, having the following
properties:
[0748] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.80 (m, 15H), 1.85-2.05 (m, 2H), 2.15-2.30
(m, 2H), 3.30-3.70 (m, 18H), 5.08 (brs, 1H).
Example 144
Synthesis of mono-O-(4,8,12-trimethyltridec-3-enyl)ascorbic
acid
##STR00137##
[0750] 0.63 mL (4.6 mmol) of triethylamine, 0.87 g (4.6 mmol) of
p-toluenesulfonyl chloride, and 20 mg (0.21 mmol) of trimethylamine
hydrochloride were added to a solution of 1.0 g (4.2 mmol) of
4,8,12-trimethyltridec-3-en-1-ol in dry methylene chloride (3 mL)
at 0.degree. C., sequentially. After being stirred for 2 hours at
room temperature, 0.10 mL (0.83 mmol) of
N,N-dimethyl-1,3-propanediamine was added to the reaction mixture
at 0.degree. C. After being stirred for 30 min, the mixture was
diluted with ethyl acetate. The resulting solution was washed with
water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous
solution, and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated to obtain (4,8,12-trimethyltridec-3-enyl)tosylate as a
crude product.
[0751] 0.63 mL (4.6 mmol) of triethylamine was added and dissolved
in a suspension of 0.73 g (4.2 mmol) of ascorbic acid in
acetonitrile (9 mL). After the above crude product of
(4,8,12-trimethyltridec-3-enyl)tosylate was added at room
temperature, the reaction mixture was heated for 2 hours at
90.degree. C. The reaction mixture was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title compound.
The results of NMR analysis of the obtained compound are as shown
below.
[0752] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.63 and 1.69 (s, 3H,
4-CH.sub.3), 1.90-2.10 (m, 2H), 2.46 (td, J=6.8, 7.4 Hz, 2H), 3.63
(d, J=6.6 Hz, 2H), 3.82 (t, J=6.6 Hz, 1H), 4.30-4.53 (m, 2H), 4.74
(s, 1H), 5.17 (t, J=6.8 Hz, 1H).
Example 145
Synthesis of methyl 3,7,11-trimethyldodec-2-enoate
##STR00138##
[0754] Under a nitrogen atmosphere, 9.0 mL (0.10 mol) of oxalyl
chloride was dissolved in methylene chloride (170 mL), and 18 mL
(0.25 mol) of dimethyl sulfoxide was slowly added dropwise to the
mixture at -78.degree. C. After the mixture was stirred for 15 min,
19.7 g (87.0 mmol) of tetrahydrofarnesol was added, followed by
stirring for 1 hour at the same temperature. After addition of 48
mL (0.35 mol) of triethylamine, the reaction mixture was allowed to
warm up to room temperature. The methylene chloride was
concentrated and diluted with diethylether. The solution was washed
with saturated brine, and dried over anhydrous sodium sulfate.
After filtration, the filtrate was concentrated to obtain
3,7,11-trimethyldodec-2-en-1-al as a crude product.
[0755] The above obtained crude product of
3,7,11-trimethyldodec-2-en-1-al was dissolved in t-butanol (90 mL)
and water (90 mL). 20.4 g (0.131 mmol) of sodium dihydrogen
phosphate, 10.1 g (0.104 mmol) of amidosulfuric acid, 9.4 g (0.10
mmol) of sodium chlorite were added to the solution. After being
stirred for 3 hours at room temperature, the reaction mixture was
diluted with ether. The solution was washed with water and
saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated to obtain
3,7,11-trimethyldodec-2-enoic acid as a crude product.
[0756] The above obtained crude product of
3,7,11-trimethyldodec-2-enoic acid was dissolved in methanol (220
mL), and concentrated sulfuric acid (0.5 mL) was added. After being
stirred for 13 hours at 60.degree. C., sodium bicarbonate was
slowly added to the reaction mixture and the mixture was confirmed
to be neutralized. After filtration, the filtrate was concentrated,
and then diluted with ethyl acetate. The solution was washed with
water and saturated brine, successively, and dried over anhydrous
sodium sulfate. After filtration, the filtrate was concentrated,
and the resulting residue was purified by silica gel column
chromatography (ethyl acetate/hexane mixture) to obtain 10.7 g of
the title compound (48% yield in 3 steps) as a slightly yellow
liquid. The results of NMR analysis of the obtained compound are as
shown below.
[0757] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.88 and 2.15 (s, 3H,
3-CH.sub.3), 2.11 (t, J=7.2 Hz, 1.1H, 4-CH.sub.2), 2.60 (t, J=7.9
Hz, 0.9H, 4-CH.sub.2), 3.67 and 3.69 (s, 3H, OMe), 5.66 and 5.67
(s, 1H, 2-CH).
Example 146
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enoyl)glycerol
##STR00139##
[0759] 0.90 g (3.5 mmol) of methyl 3,7,11-trimethyldodec-2-enoate
was slowly added dropwise to a solution of 0.59 g (6.4 mmol) of
glycerol and 0.88 g (6.4 mmol) of potassium carbonate in dry
N,N-dimethylformamide (3 mL) at 100.degree. C. After the reaction
mixture was stirred at 100.degree. C. for 18 hours, 1M hydrochloric
acid was added. The resulting solution was extracted with ether,
and the extract was washed with saturated sodium bicarbonate
aqueous solution and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated, and the resulting residue was purified by silica gel
column chromatography (ethyl acetate/hexane mixture) to obtain 318
mg of the title compound (29% yield) as a colorless viscous
product.
[0760] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0761] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.80 (m, 12H), 1.91 and 2.16 (s, 3H,
3-CH.sub.3), 2.10-2.20 (m, 2H), 2.61 (brs, OH), 3.50-4.00 (m, 3H),
4.10-4.30 (m, 2H), 5.70 (brs, 1H).
Example 147
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enoyl)erythritol
##STR00140##
[0763] The title compound was synthesized using the same procedure
as employed in Example 146, but with 0.78 g (6.4 mmol) of
erythritol instead of glycerol. The compound was obtained (283 mg,
23% yield) having the following properties:
[0764] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.80 (m, 12H), 1.92 and 2.17 (s, 3H,
3-CH.sub.3), 2.10-2.20 (in, 2H), 3.60-4.00 (m, 4H), 4.20-4.45 (m,
2H), 5.72 (brs, 1H).
Example 148
Synthesis of
mono-O-(3,7,11-trimethyldodec-2-enoyl)pentaerythritol
##STR00141##
[0766] The title compound was synthesized using the same procedure
as employed in Example 146, but with 0.87 g (6.4 mmol) of
pentaerythritol instead of glycerol. The compound was obtained (459
mg, 36% yield) having the following properties:
[0767] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.80 (m, 12H), 1.92 and 2.17 (s, 3H,
3-CH.sub.3), 2.10-2.20 (m, 2H), 2.70 (brs, 30H), 3.65 (s, 6H),
4.20-4.30 (in, 2H), 5.70 (brs, 1H).
Example 149
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enoyl)diglycerol
##STR00142##
[0769] 0.90 g (3.5 mmol) of methyl 3,7,11-trimethyldodec-2-enoate
was slowly added dropwise to a solution of 1.06 g (6.37 mmol) of
diglycerol and 0.88 g (6.4 mmol) of potassium carbonate in dry
N,N-dimethylformamide (3 mL) at 100.degree. C. After the reaction
mixture was stirred at 100.degree. C. for 18 hours, 1M hydrochloric
acid was added. The resulting solution was extracted with ethyl
acetate, and the extract was washed with saturated sodium
bicarbonate aqueous solution and saturated brine, successively, and
dried over anhydrous sodium sulfate. After filtration, the filtrate
was concentrated, and the resulting residue was purified by silica
gel column chromatography (methanol/methylene chloride mixture) to
obtain 322 mg of the title compound (23% yield) as a slightly
yellow viscous product.
[0770] The results of 1H-NMR analysis of the obtained compound are
as shown below.
[0771] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.80 (m, 12H), 1.90 and 2.16 (s, 3H,
3-CH.sub.3), 2.10-2.20 (m, 2H), 3.40-4.30 (m, 10H), 5.70 (brs,
1H).
Example 150
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enoyl)triglycerol
##STR00143##
[0773] The title compound was synthesized using the same procedure
as employed in Example 149, but with 1.53 g (6.4 mmol) of
triglycerol instead of diglycerol. The compound was obtained (291
mg, 18% yield) having the following properties:
[0774] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.80 (m, 12H), 1.90 and 2.15 (s, 3H,
3-CH.sub.3), 2.10-2.20 (m, 2H), 3.45-4.20 (m, 15H), 5.70 (brs,
1H).
Example 151
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enoyl)xylitol
##STR00144##
[0776] The title compound was synthesized using the same procedure
as employed in Example 149, but with 0.97 g (6.4 mmol) of xylitol
instead of diglycerol. The compound was obtained (169 mg, 13%
yield) having the following properties:
[0777] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.95 (m, 9H), 1.00-1.80 (m, 12H), 1.90 and 2.16 (s, 3H,
3-CH.sub.3), 2.10-2.20 (m, 2H), 3.30-4.40 (m, 7H), 5.69 (brs,
1H).
Example 152
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enoyl)mannitol
##STR00145##
[0779] The title compound was synthesized using the same procedure
as employed in Example 149, but with 1.16 g (6.37 mmol) of mannitol
instead of diglycerol. The compound was obtained (183 mg, 13%
yield) having the following properties:
[0780] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3+3% CD.sub.3OD,
TMS) .delta.: 0.80-0.95 (m, 9H), 1.00-1.80 (m, 12H), 1.91 and 2.16
(s, 3H, 3-CH.sub.3), 2.10-2.20 (m, 2H), 3.65-3.95 (m, 6H),
4.20-4.45 (m, 2H), 5.74 (brs, 1H).
Example 153
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enoyl)sorbitol
##STR00146##
[0782] The title compound was synthesized using the same procedure
as employed in Example 149, but with 1.16 g (6.37 mmol) of sorbitol
instead of diglycerol. The compound was obtained (184 mg, 13%
yield) having the following properties:
[0783] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.80 (m, 12H), 1.90-2.20 (m, 5H), 3.60-4.40
(m, 8H), 5.72 (brs, 1H).
Example 154
Synthesis of
mono-O-(3,7,11-trimethyldodec-2-enoyl)dipentaerythritol
##STR00147##
[0785] The title compound was synthesized using the same procedure
as employed in Example 149, but with 1.62 g (6.37 mmol) of
dipentaerythritol instead of diglycerol. The compound was obtained
(101 mg, 6% yield) having the following properties:
[0786] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3+3% CD.sub.3OD,
TMS) .delta.: 0.80-0.90 (m, 9H), 1.00-1.80 (m, 12H), 1.91 and 2.16
(s, 3H, 3-CH.sub.3), 2.10-2.20 (m, 2H), 3.35-3.45 (m, 4H),
3.50-3.60 (m, 8H), 4.08 (d, J=4.7 Hz, 2H), 5.68 (brs, 1H).
Example 155
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enoyl)ascorbic
acid
##STR00148##
[0788] 0.69 g (3.9 mmol) of ascorbic acid was dissolved in
concentrated sulfuric acid (18 mL). After addition of 1.0 g (3.9
mmol) of methyl 3,7,11-trimethyldodec-2-enoate, the mixture was
stirred for 24 hours at room temperature. The reaction mixture was
poured into iced water, and extracted with ethyl acetate. The
extract was washed with water, 1M hydrochloric acid, saturated
sodium bicarbonate aqueous solution, and saturated brine,
successively, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated, and the resulting
residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 156
Synthesis of 1-O-(3,7,11-trimethyldodec-2-enyl)-D-glucoside
##STR00149##
[0790] 2.24 g (5.74 mmol) of .beta.-D-glucose pentaacetate and 1.0
g (4.4 mmol) of tetrahydrofarnesol were dissolved in dry
acetonitrile (8 mL). 1.12 mL (8.83 mmol) of boron trifluoride
diethyl etherate complex was added to the solution with cooling on
ice. The reaction mixture was allowed to warm up slowly to room
temperature while being stirred for 24 hours before addition of 1.8
mL (13 mmol) of triethylamine at 0.degree. C. The resulting
solution was diluted with ethyl acetate, and washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over sodium sulfate.
After filtration, the filtrate was concentrated to obtain
1-O-(3,7,11-trimethyldodec-2-enyl)-D-glucopyranoside tetraacetate
as a crude product.
[0791] The above obtained crude product of
1-O-(3,7,11-trimethyldodec-2-enyl)-D-glucopyranoside tetraacetate
was dissolved in methanol/tetrahydrofuran (1:1, 6 mL), and 0.45 mL
(0.45 mmol) of 1M sodium methylate in methanol was added at room
temperature. After being stirred for 24 hours, 33 .mu.L (0.46 mmol)
of acetyl chloride was added to the reaction mixture and the
mixture was confirmed to be neutralized. After addition of water,
the solution was extracted with ethyl acetate. The extract was
washed with saturated brine, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 157
Synthesis of
1-O-(3,7,11-trimethyldodec-2-enyl)-D-xylopyranoside
##STR00150##
[0793] The title compound was synthesized using the same procedure
as employed in Example 156, but with 1.83 g (5.74 mmol) of D-xylose
tetraacetate instead of .beta.-D-glucose pentaacetate.
Example 158
Synthesis of 1-O-(3,7,11-trimethyldodec-2-enyl)-D-galactoside
##STR00151##
[0795] The title compound was synthesized using the same procedure
as employed in Example 156, but with 2.24 g (5.74 mmol) of
D-galactose pentaacetate instead of .beta.-D-glucose
pentaacetate.
Example 159
Synthesis of 1-O-(3,7,11-trimethyldodec-2-enyl)-D-mannoside
##STR00152##
[0797] The title compound was synthesized using the same procedure
as employed in Example 156, but with 2.24 g (5.74 mmol) of
D-mannose pentaacetate instead of .beta.-D-glucose
pentaacetate.
Example 160
Synthesis of 1-O-(3,7,11-trimethyldodec-2-enyl)-D-maltoside
##STR00153##
[0799] 3.9 g (5.7 mmol) of D-Maltose octaacetate and 1.0 g (4.4
mol) of tetrahydrofarnesol was dissolved in dry acetonitrile (4
mL). 1.12 mL (8.83 mmol) of boron trifluoride diethyl etherate
complex was added to the solution with cooling on ice. The reaction
mixture was allowed to warm up slowly to room temperature while
being stirred for 24 hours before addition of 1.8 mL (13 mmol) of
triethylamine at 0.degree. C. The resulting solution was diluted
with ethyl acetate, and washed with water, 1M hydrochloric acid,
saturated sodium bicarbonate aqueous solution, and saturated brine,
successively, and dried over sodium sulfate. After filtration, the
filtrate was concentrated to obtain
1-O-(3,7,11-trimethyldodec-2-enyl)-D-maltoside heptaacetate as a
crude product.
[0800] The above obtained crude product of
1-O-(3,7,11-trimethyldodec-2-enyl)-D-maltoside heptaacetate was
dissolved in methanol/tetrahydrofuran (1:1, 6 mL), and 0.45 mL
(0.45 mmol) of 1M sodium methylate in methanol was added at room
temperature. After being stirred for 24 hours, 33 .mu.L (0.46 mmol)
of acetyl chloride was added to the reaction mixture and the
mixture was confirmed to be neutralized. The mixture was
concentrated, and the resulting residue was purified by silica gel
column chromatography (methanol/methylene chloride mixture) to
obtain the title compound.
Example 161
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enyl)glycerol
##STR00154##
[0802] 1.18 g (8.84 mmol) of N-chlorosuccinimide was suspended in
methylene chloride (13 mL). After addition of 0.69 mL (9.3 mmol) of
dimethylsulfide at 0.degree. C., the solution was stirred for 20
min. After addition of 1.0 g (4.4 mmol) of tetrahydrofarnesol, the
mixture was stirred for 1 hour at 0.degree. C., with additional
stirring for 6 hours at room temperature. After addition of
saturated sodium bicarbonate aqueous solution, the reaction mixture
was extracted with methylene chloride. The extract was washed with
saturated brine, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated to obtain
3,7,11-trimethyldodec-2-ene-1-chloride as a crude product.
[0803] 0.29 g (55%, 6.6 mmol) of sodium hydride was added to a
solution of 0.61 g (6.6 mmol) of glycerol in dry
N,N-dimethylformamide/tetrahydrofuran (1:1, 4 mL) at 0.degree. C.
with cooling on ice. After the mixture was stirred for 30 min at
50.degree. C., the above 3,7,11-trimethyldodec-2-ene-1-chloride was
added dropwise with additional stirring for 20 hours at the same
temperature. After addition of water at 0.degree. C., the reaction
mixture was extracted with ether. The extract was washed with
water, 1M hydrochloric acid, saturated sodium bicarbonate aqueous
solution, and saturated brine, successively, and dried over
anhydrous sodium sulfate. After filtration, the filtrate was
concentrated, and the resulting residue was purified by silica gel
column chromatography (ethyl acetate/hexane mixture) to obtain the
title compound.
Example 162
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enyl)erythritol
##STR00155##
[0805] The title compound was synthesized using the same procedure
as employed in Example 161, but with 0.81 g (6.6 mmol) of
erythritol instead of glycerol.
Example 163
Synthesis of
mono-O-(3,7,11-trimethyldodec-2-enyl)pentaerythritol
##STR00156##
[0807] The title compound was synthesized using the same procedure
as employed in Example 161, but with 0.90 g (6.6 mmol) of
pentaerythritol instead of glycerol, having the following
properties:
[0808] .sup.1H-NMR spectrum (300 MHz, CDCl.sub.3, TMS) .delta.:
0.80-0.90 (m, 9H), 1.00-1.60 (m, 12H), 1.65 and 1.74 (s, 3H,
3-CH.sub.3), 1.95-2.05 (m, 2H), 2.87 (brs, 3H, OH), 3.45 (s, 2H),
3.72 (s, 6H), 3.97 (d, J=7.3 Hz, 2H), 5.29 (t, J=7.3 Hz, 1H).
Example 164
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enyl)diglycerol
##STR00157##
[0810] 1.18 g (8.84 mmol) of N-Chlorosuccinimide was suspended in
methylene chloride (13 mL). After addition of 0.69 mL (9.3 mmol) of
dimethylsulfide at 0.degree. C., the solution was stirred for 20
min. After addition of 1.0 g (4.4 mmol) of tetrahydrofarnesol, the
mixture was stirred for 1 hour at 0.degree. C., with additional
stirring for 6 hours at room temperature. After addition of
saturated sodium bicarbonate aqueous solution, the reaction mixture
was extracted with methylene chloride. The extract was washed with
saturated brine, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated to obtain
3,7,11-trimethyldodec-2-ene-1-chloride as a crude product.
[0811] 0.29 g (55%, 6.6 mmol) of sodium hydride was added to a
solution of 1.1 g (6.6 mmol) of diglycerol in dry
N,N-dimethylformamide/tetrahydrofuran (1:1, 4 mL) with cooling on
ice. After the mixture was stirred for 30 min at 50.degree. C., the
above 3,7,11-trimethyldodec-2-ene-1-chloride was added dropwise
with additional stirring for 20 hours at the same temperature.
After addition of water at 0.degree. C., the reaction mixture was
extracted with ether. The extract was washed with water, 1M
hydrochloric acid, saturated sodium bicarbonate aqueous solution,
and saturated brine, successively, and dried over anhydrous sodium
sulfate. After filtration, the filtrate was concentrated, and the
resulting residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 165
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enyl)triglycerol
##STR00158##
[0813] The title compound was synthesized using the same procedure
as employed in Example 164, but with 1.6 g (6.6 mmol) of
triglycerol instead of diglycerol.
Example 166
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enyl)xylitol
##STR00159##
[0815] The title compound was synthesized using the same procedure
as employed in Example 164, but with 1.0 g (6.6 mmol) of xylitol
instead of diglycerol.
Example 167
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enyl)mannitol
##STR00160##
[0817] The title compound was synthesized using the same procedure
as employed in Example 164, but with 1.2 g (6.6 mmol) of mannitol
instead of diglycerol.
Example 168
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enyl)sorbitol
##STR00161##
[0819] The title compound was synthesized using the same procedure
as employed in Example 164, but with 1.2 g (6.6 mmol) of sorbitol
instead of diglycerol.
Example 169
Synthesis of
mono-O-(3,7,11-trimethyldodec-2-enyl)dipentaerythritol
##STR00162##
[0821] The title compound was synthesized using the same procedure
as employed in Example 164, but with 1.7 g (6.6 mmol) of
dipentaerythritol instead of diglycerol.
Example 170
Synthesis of mono-O-(3,7,11-trimethyldodec-2-enyl)ascorbic acid
##STR00163##
[0823] 1.18 g (8.84 mmol) of N-Chlorosuccinimide was suspended in
methylene chloride (13 mL). After addition of 0.69 mL (9.3 mmol) of
dimethylsulfide at 0.degree. C., the solution was stirred for 20
min. After addition of 1.0 g (4.4 mmol) of tetrahydrofarnesol, the
mixture was stirred for 1 hour at 0.degree. C., with additional
stirring for 6 hours at room temperature. After addition of
saturated sodium bicarbonate aqueous solution, the reaction mixture
was extracted with methylene chloride. The extract was washed with
saturated brine, and dried over anhydrous sodium sulfate. After
filtration, the filtrate was concentrated to obtain
3,7,11-trimethyldodec-2-ene-1-chloride as a crude product.
[0824] 0.66 mL (4.8 mmol) of triethylamine was added and dissolved
in a suspension of 0.77 g (4.4 mmol) of ascorbic acid in
acetonitrile (9 mL). After the above crude product of
3,7,11-trimethyldodec-2-ene-1-chloride was added at room
temperature, the reaction mixture was heated for 2 hours at
90.degree. C. The reaction mixture was concentrated, and resulting
the residue was purified by silica gel column chromatography
(methanol/methylene chloride mixture) to obtain the title
compound.
Example 171
Formation of a liquid crystal by
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)glycerol and analysis
thereof
[0825] Mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)glycerol
synthesized in Example 3 and water were homogeneously mixed in
accordance with the same procedure as in Example 13 to obtain a
sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)glycerol/water system.
SAXS analysis of the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)glycerol/water system
was performed in the same manner as in Example 13. As a result,
scattering peaks were observed. The peak value ratio exhibited the
following ratio peculiar to the cubic liquid crystal belonging to
the crystallographic space group Pn3m:
{square root over (2)}: {square root over (3)}: {square root over
(4)}.
[0826] Thus, the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)glycerol/water system
was confirmed to form a cubic liquid crystal that belong to the
crystallographic space group Pn3m.
Example 172
Formation of a liquid crystal by
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)diglycerol and analysis
thereof
[0827] Mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)diglycerol
synthesized in Example 32 and water were homogeneously mixed in
accordance with the same procedure as in Example 13 to obtain a
sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)diglycerol/water
system. SAXS analysis of the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)diglycerol/water system
was performed in the same manner as in Example 13. As a result,
scattering peaks were observed. The peak value ratio exhibited the
following ratio peculiar to the cubic liquid crystal belonging to
the crystallographic space group Pn3m:
{square root over (2)}: {square root over (3)}: {square root over
(4)}.
[0828] Thus, the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enyl)diglycerol/water system
was confirmed to form a cubic liquid crystal that belong to the
crystallographic space group Pn3m.
Example 173
Formation of a liquid crystal by
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-xylopyranoside and analysis
thereof
[0829] 1-O-(5,9,13-trimethyltetradec-4-enyl)-D-xylopyranoside
synthesized in Example 103 and water were homogeneously mixed in
accordance with the same procedure as in Example 13 to obtain a
sample of
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-xylopyranoside/water
system. SAXS analysis of the sample of
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-xylopyranoside/water system
was performed in the same manner as in Example 13. As a result,
scattering peaks were observed. The peak value ratio exhibited the
following ratio peculiar to the cubic liquid crystal belonging to
the crystallographic space group Pn3m:
{square root over (2)}: {square root over (3)}: {square root over
(4)}.
[0830] Thus, the sample of
1-O-(5,9,13-trimethyltetradec-4-enyl)-D-xylopyranoside/water system
was confirmed to form a cubic liquid crystal that belong to the
crystallographic space group Pn3m.
Example 174
Formation of a liquid crystal by
mono-O-(5,9,13-trimethyltetradec-4-enyl)glycerol and analysis
thereof
[0831] Mono-O-(5,9,13-trimethyltetradec-4-enyl)glycerol synthesized
in Example 107 and water were homogeneously mixed in accordance
with the same procedure as in Example 13 to obtain a sample of
mono-O-(5,9,13-trimethyltetradec-4-enyl)glycerol/water system. SAXS
analysis of the sample of
mono-O-(5,9,13-trimethyltetradec-4-enyl)glycerol/water system was
performed in the same manner as in Example 13. As a result,
scattering peaks were observed. The peak value ratio exhibited the
following ratio peculiar to the reverse hexagonal liquid
crystal:
1: {square root over (3)}:2.
[0832] Thus, the sample of
mono-O-(5,9,13-trimethyltetradec-4-enyl)glycerol/water system was
confirmed to form a reverse hexagonal liquid crystal.
Example 175
Formation of a liquid crystal by
mono-O-(4,8,12-trimethyltridec-3-enoyl)glycerol and analysis
thereof
[0833] Mono-O-(4,8,12-trimethyltridec-3-enoyl)glycerol synthesized
in Example 120 and water were homogeneously mixed in accordance
with the same procedure as in Example 13 to obtain a sample of
mono-O-(4,8,12-trimethyltridec-3-enoyl)glycerol/water system. SAXS
analysis of the sample of
mono-O-(4,8,12-trimethyltridec-3-enoyl)glycerol/water system was
performed in the same manner as in Example 13. As a result,
scattering peaks were observed. The peak value ratio exhibited the
following ratio peculiar to the cubic liquid crystal belonging to
the crystallographic space group Pn3m:
{square root over (2)}: {square root over (3)}: {square root over
(4)}.
[0834] Thus, the sample of
mono-O-(4,8,12-trimethyltridec-3-enoyl)glycerol/water system was
confirmed to form a cubic liquid crystal that belong to the
crystallographic space group Pn3m.
Example 176
Formation of a liquid crystal by
mono-O-(5,9,13-trimethyltetradec-4-enoyl)glycerol and analysis
thereof
[0835] Mono-O-(5,9,13-trimethyltetradec-4-enoyl)glycerol
synthesized in Example 92 and water were homogeneously mixed in
accordance with the same procedure as in Example 13 to obtain a
sample of mono-O-(5,9,13-trimethyltetradec-4-enoyl)glycerol/water
system. SAXS analysis of the sample of
mono-O-(5,9,13-trimethyltetradec-4-enoyl)glycerol/water system was
performed in the same manner as in Example 13. As a result,
scattering peaks were observed. The peak value ratio exhibited the
following ratio peculiar to the cubic liquid crystal belonging to
the crystallographic space group Pn3m:
{square root over (2)}: {square root over (3)}: {square root over
(4)}
and the following ratio peculiar to the reverse hexagonal liquid
crystal:
1: {square root over (3)}:2.
[0836] Thus, the sample of
mono-O-(5,9,13-trimethyltetradec-4-enoyl)glycerol/water system was
confirmed to form a mixture of a cubic liquid crystal that belong
to the crystallographic space group Pn3m and a reverse hexagonal
liquid crystal.
Example 177
Formation of a liquid crystal by
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)diglycerol and
analysis thereof
[0837] Mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)diglycerol
synthesized in Example 4 and water were homogeneously mixed in
accordance with the same procedure as in Example 13 to obtain a
sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)diglycerol/water
system. SAXS analysis of the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)diglycerol/water
system was performed in the same manner as in Example 13. As a
result, scattering peaks were observed. The peak value ratio
exhibited the following ratio peculiar to the reverse hexagonal
liquid crystal:
1: {square root over (3)}:2.
[0838] Thus, the sample of
mono-O-(5,9,13,17-tetramethyloctadec-4-enoyl)diglycerol/water
system was confirmed to form a reverse hexagonal liquid
crystal.
Example 178
Formation of a liquid crystal by
mono-O-(3,7,11-trimethyldodec-2-enoyl)glycerol and analysis
thereof
[0839] Mono-O-(3,7,11-trimethyldodec-2-enoyl)glycerol synthesized
in Example 146 and water were homogeneously mixed in accordance
with the same procedure as in Example 13 to obtain a sample of
mono-O-(3,7,11-trimethyldodec-2-enoyl)glycerol/water system. SAXS
analysis of the sample of
mono-O-(3,7,11-trimethyldodec-2-enoyl)glycerol/water system was
performed in the same manner as in Example 13. As a result,
scattering peaks were observed. The peak value ratio exhibited the
following ratio peculiar to the cubic liquid crystal belonging to
the crystallographic space group Pn3m:
{square root over (2)}: {square root over (3)}: {square root over
(4)}.
[0840] Thus, the sample of
mono-O-(3,7,11-trimethyldodec-2-enoyl)glycerol/water system was
confirmed to form a cubic liquid crystal that belong to the
crystallographic space group Pn3m.
Example 179
[0841] Viscosity measurement of the amphiphilic compounds
[0842] The viscosities of the amphiphilic compounds synthesized
above were measured at 25.degree. C. and at a shear velocity of
105.7 s.sup.-1 using a viscosity and viscoelasticity measuring
apparatus MARS (Thermo Fisher Scientific). The representative
results of the measurement are shown in Table 1.
TABLE-US-00001 TABLE 1 Compound Viscosity (Pas sec) Example 4 4.5
Example 31 0.44 Example 65 1.1 Example 67 10.6 Example 68 9.5
Example 80 0.45 Example 82 4.0 Example 92 0.48 Example 95 10.5
Example 109 0.98 Example 110 1.7 Example 146 0.45 Example 147 7.1
Example 149 6.9 Example 163 2.7 Example 166 1.1
[0843] These results confirmed that the amphiphilic compounds of
this invention had very low viscosities.
* * * * *