Method for producing glycoside compounds
The invention provides a production method of a glycoside compound or a salt thereof, which includes subjecting a thioether compound and an alcohol compound to a coupling reaction in the presence of a halogenating agent, a desiccant and a Lewis acid, and then distillation in the presence of at least one kind of additive selected from a sulfur-containing antioxidant and a maleimide group-containing compound to give a thioether compound and a step of subjecting a glycoside compound and a thioether compound to a coupling reaction in the presence of a halogenating agent, a desiccant and a Lewis acid to give a glycoside compound. By this method, a phosphoramidite preferable for the production (synthesis) of a nucleic acid can be produced more efficiently at a high purity.
1. A method of producing a glycoside compound represented by the formula (I):
wherein R 1 is a hydroxyl-protecting group; R 2a and R 2b are the same or different and each is a hydrogen atom or a substituent; R 2c is a hydrogen atom, an electron-withdrawing group or a substituent optionally substituted by an electron-withdrawing group; R 2a and R 2b optionally form a ring together with a nitrogen atom bonded thereto; B is an atomic group having a nucleic acid base skeleton; L 1 is an alkylene group; D 1 is an electron-withdrawing group; and m is a positive integer, or a salt thereof, comprising
a step of subjecting
a thioether compound represented by the formula (103):
wherein m is as defined above; and R and R′ are the same or different and each is an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an aralkyl group, a cycloalkyl group, a cycloalkenyl group, a cycloalkylalkyl group, a cycloalkenylalkyl group or an alkoxyalkyl group, and
an alcohol compound represented by the formula (105):
wherein each symbol is as defined above,
to a coupling reaction in the presence of a halogenating agent, a desiccant and a Lewis acid, and then to distillation in the presence of at least one maleimide group-containing compound to give a thioether compound represented by the formula (104):
wherein each symbol is as defined above (Step 0); and
a step of subjecting a glycoside compound represented by the formula (Ia):
wherein B is as defined above; and X is a group represented by the following formula:
wherein n is 0 or 1; and R 1a -R 1d are the same or different and each is a hydrogen atom, an alkyl group or an alkoxy group, and a thioether compound represented by the formula (104)
to a coupling reaction in the presence of a halogenating agent, a desiccant and a Lewis acid to give a glycoside compound represented by the formula (Ib):
wherein each symbol is as defined above (Step 1).
2. The production method according to claim 1 , further comprising a step of deprotecting the compound represented by the formula (Ib) to give a glycoside compound represented by the formula (Ic):
wherein each symbol is as defined in claim 1 (Step 2).
3. The production method according to claim 2 , further comprising a step of introducing a hydroxyl-protecting group into the glycoside compound represented by the formula (Ic) to give a glycoside compound represented by the formula (Id):
wherein each symbol is as defined in claim 1 (Step 3).
4. The production method according to claim 3 , further comprising a step of phosphorylating the glycoside compound represented by the formula (Id) to give glycoside compound represented by the formula (I) (Step 4).
5. A method of producing a glycoside compound represented by the formula (Ib):
wherein B is an atomic group having a nucleic acid base skeleton; L 1 is an alkylene group; D 1 is an electron-withdrawing group; and m is a positive integer, comprising
a step of subjecting
a thioether compound represented by the formula (103):
wherein m is as defined above; and R and R′ are the same or different and each is an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an aralkyl group, a cycloalkyl group, a cycloalkenyl group, a cycloalkylalkyl group, a cycloalkenylalkyl group or an alkoxyalkyl group, and
an alcohol compound represented by the formula (105):
wherein each symbol is as defined above,
to a coupling reaction in the presence of a halogenating agent, a desiccant and a Lewis acid, and then to distillation in the presence of at least one maleimide group-containing compound to give a thioether compound represented by the formula (104):
wherein each symbol is as defined above (Step 0); and
a step of subjecting a glycoside compound represented by the formula (Ia):
wherein B is as defined above; and X is a group represented by the following formula:
wherein n is 0 or 1; and R 1a -R 1d are the same or different and each is a hydrogen atom, an alkyl group or an alkoxy group, and a thioether compound represented by the formula (104)
to a coupling reaction in the presence of a halogenating agent, a desiccant and a Lewis acid (Step 1).
6. A method of producing a glycoside compound represented by the formula (Ic):
wherein B is an atomic group having a nucleic acid base skeleton; L 1 is an alkylene group; D 1 is an electron-withdrawing group; and m is a positive integer, comprising
a step of subjecting a thioether compound represented by the formula (103):
wherein m is as defined above; and R and R′ are the same or different and each is an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an aralkyl group, a cycloalkyl group, a cycloalkenyl group, a cycloalkylalkyl group, a cycloalkenylalkyl group or an alkoxyalkyl group, and
an alcohol compound represented by the formula (105):
wherein each symbol is as defined above,
to a coupling reaction in the presence of a halogenating agent, a desiccant and a Lewis acid, and then to distillation in the presence of at least one maleimide group-containing compound to give a thioether compound represented by the formula (104):
wherein each symbol is as defined above (Step 0); and
a step of subjecting a glycoside compound represented by the formula (Ia):
wherein B is as defined above; and X is a group represented by the following formula:
wherein n is 0 or 1; and R 1a -R 1d are the same or different and each is a hydrogen atom, an alkyl group or an alkoxy group, and a thioether compound represented by the formula (104)
to a coupling reaction in the presence of a halogenating agent, a desiccant and a Lewis acid to give a glycoside compound represented by the formula (Ib):
wherein each symbol is as defined above (Step 1); and
a step of deprotecting the glycoside compound represented by the formula (Ib) (Step 2).
7. A method of producing a glycoside compound represented by the formula (Id):
wherein R 1 is a hydroxyl-protecting group; B is an atomic group having a nucleic acid base skeleton; L 1 is an alkylene group; D 1 is an electron-withdrawing group; and m is a positive integer, comprising
a step of subjecting a thioether compound represented by the formula (103):
wherein m is as defined above; and R and R′ are the same or different and each is an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an aralkyl group, a cycloalkyl group, a cycloalkenyl group, a cycloalkylalkyl group, a cycloalkenylalkyl group or an alkoxyalkyl group, and an alcohol compound represented by the formula (105):
wherein each symbol is as defined above,
to a coupling reaction in the presence of a halogenating agent, a desiccant and a Lewis acid, and then to distillation in the presence of at least one maleimide group-containing compound to give a thioether compound represented by the formula (104):
wherein each symbol is as defined above (Step 0); and
a step of subjecting a glycoside compound represented by the formula (Ia):
wherein B is as defined above; and X is a group represented by the following formula:
wherein n is 0 or 1; and R 1a -R 1d are the same or different and each is a hydrogen atom, an alkyl group or an alkoxy group, and a thioether compound represented by the formula (104)
to a coupling reaction in the presence of a halogenating agent, a desiccant and a Lewis acid to give a glycoside compound represented by the formula (Ib):
wherein each symbol is as defined above (Step 1);
a step of deprotecting the glycoside compound represented by the formula (Ib) to give a glycoside compound represented by the formula (Ic):
wherein each symbol is as defined above (Step 2); and
a step of introducing a hydroxyl-protecting group into the glycoside compound represented by the formula (Ic) (Step 3).
8. The method according to claim 1 , wherein the maleimide group-containing compound in the distillation in Step 0 is 4,4′-bismaleimidodiphenylmethane.
9. The method according to claim 1 , wherein n is 1.
10. The method according to claim 1 , wherein R 1a -R 1d are isopropyl groups.
11. The method according to claim 1 , wherein m is 1.
12. The method according to claim 1 , wherein L 1 is an ethylene group.
13. The method according to claim 1 , wherein D 1 is a cyano group.
14. The method according to claim 1 , wherein the thioether compound represented by the formula (104) is added after the addition of the halogenating agent, the desiccant and the Lewis acid in Step 1.
15. The method according to claim 1 , wherein the halogenating agent is added after the addition of the desiccant, the Lewis acid and the thioether compound represented by the formula (104) in Step 1.
16. The method according to claim 14 , wherein the Lewis acid is added after the addition of the halogenating agent in Step 1.
17. The method according to claim 15 , wherein the thioether compound represented by the formula (104) is added after the addition of the Lewis acid in Step 1.
18. The method according to claim 1 , wherein the halogenating agent in Step 1 is an iodinating agent.
19. The method according to claim 18 , wherein the iodinating agent is 1,3-diiodo-5,5-dimethylhydantoin or iodine.
20. The method according to claim 1 , wherein the Lewis acid in Step 1 is trifluoromethanesulfonic acid or methanesulfonic acid.