Synthetic intermediate of 1-(2-deoxy-2-fluoro-4-thio-β-D-arabinofuranosyl) cytosine, synthetic intermediate of thionucleoside, and method for producing the same

Patent metadata

Field	Value
Publication number	US-9475835-B2
Application number	US-201514873966-A
Country	US
Kind code	B2
Filing date	Oct 2, 2015
Priority date	Aug 13, 2012
Publication date	Oct 25, 2016
Grant date	Oct 25, 2016

Abstract

A compound represented by a formula [1D] as shown below (wherein R 1A , R 1B , R 2A , R 2B , R 3A and R 3B represent a hydrogen atom, an optionally substituted C 1-6 alkyl group, and the like) is useful as an intermediate for producing a thionucleoside, and the production method of the present invention is useful as a method for producing a thionucleoside.

First claim

The invention claimed is:

1. A production method of a compound represented by the following formula [1E]:

(wherein R 1A , R 1B , R 2A , R 2B , R 3A and R 3B have the same meanings as those described below) which comprises allowing a compound represented by the following formula [1D]:

(wherein R 1A and R 1B , which are the same or different, each represent a hydrogen atom, an optionally protected carboxyl group, an optionally substituted C 1-6 alkyl group, an optionally substituted C 2-6 alkenyl group, an optionally substituted C 2-6 alkynyl group, an optionally substituted aryl group or an optionally substituted heterocyclic group; R 2A and R 2B , which are the same or different, each represent a hydrogen atom, a hydroxyl group, a halogen atom, a cyano group, an azide group, an optionally protected amino group, an optionally protected carboxyl group, a group represented by the following formula [15];
—OR 2a   [15]

(wherein R 2a represents a hydroxyl-protecting group), an optionally substituted C 1-6 alkyl group, an optionally substituted C 2-6 alkenyl group, an optionally substituted C 2-6 alkynyl group, an optionally substituted C 1-6 alkoxy group, an optionally substituted C 1-6 alkylthio group, an optionally substituted aryl group, an optionally substituted aryloxy group, an optionally substituted arylthio group, an optionally substituted heterocyclic group, an optionally substituted heterocyclic oxy group or an optionally substituted heterocyclic thio group; or R 2A and R 2B may together form an optionally substituted C 1-6 alkylidene group; R 3A and R 3B , which are the same or different, each represent a hydrogen atom, a hydroxyl group, a halogen atom, a cyano group, an azide group, an optionally protected amino group, an optionally protected carboxyl group, a group represented by the following formula [16]:
—OR 3a   [16]

(wherein R 3a represents a hydroxyl-protecting group), an optionally substituted C 1-6 alkyl group, an optionally substituted C 2-6 alkenyl group, an optionally substituted C 2-6 alkynyl group, an optionally substituted C 1-6 alkoxy group, an optionally substituted C 1-6 alkylthio group, an optionally substituted aryl group, an optionally substituted aryloxy group, an optionally substituted arylthio group, an optionally substituted heterocyclic group, an optionally substituted heterocyclic oxy group or an optionally substituted heterocyclic thio group; or R 3A and R 3B may together form an optionally substituted C 1-6 alkylidene group; or R 2A and R 3A may together form a group represented by the following formula [17]:
—O—Y 1 —O—  [17]

(wherein Y 1 represents an optionally substituted C 1-6 alkylene group or an optionally substituted siloxane group; and the bond on the left side binds to a carbon atom binding to R 2A ), or a bond; and X represents a leaving group), to react with a hydrogen sulfide or a salt thereof.

2. A production method of a compound represented by the following formula [1Ea]:

(wherein R 1A , R 1B , R 2A , R 2B , R 3A and R 3B have the same meanings as those described below) which comprises allowing a compound represented by the following formula [1 Da]:

(wherein R 1A and R 1B , which are the same or different, each represent a hydrogen atom, an optionally protected carboxyl group, an optionally substituted C 1-6 alkyl group, an optionally substituted C 2-6 alkenyl group, an optionally substituted C 2-6 alkynyl group, an optionally substituted aryl group or an optionally substituted heterocyclic group; R 2A and R 2B , which are the same or different, each represent a hydrogen atom, a hydroxyl group, a halogen atom, a cyano group, an azide group, an optionally protected amino group, an optionally protected carboxyl group, a group represented by the following formula [15]:
—OR 2a   [15]

(wherein R 2a represents a hydroxyl-protecting group), an optionally substituted C 1-6 alkyl group, an optionally substituted C 2-6 alkenyl group, an optionally substituted C 2-6 alkynyl group, an optionally substituted C 1-6 alkoxy group, an optionally substituted C 1-6 alkylthio group, an optionally substituted aryl group, an optionally substituted aryloxy group, an optionally substituted arylthio group, an optionally substituted heterocyclic group, an optionally substituted heterocyclic oxy group or an optionally substituted heterocyclic thio group; or R 2A and R 2B may together form an optionally substituted C 1-6 alkylidene group; R 3A and R 3B , which are the same or different, each represent a hydrogen atom, a hydroxyl group, a halogen atom, a cyano group, an azide group, an optionally protected amino group, an optionally protected carboxyl group, a group represented by the following formula [16];
—OR 3a   [16]

(wherein R 3a represents a hydroxyl-protecting group), an optionally substituted C 1-6 alkyl group, an optionally substituted C 2-6 alkenyl group, an optionally substituted C 2-6 alkynyl group, an optionally substituted C 1-6 alkoxy group, an optionally substituted C 1-6 alkylthio group, an optionally substituted aryl group, an optionally substituted aryloxy group, an optionally substituted arylthio group, an optionally substituted heterocyclic group, an optionally substituted heterocyclic oxy group or an optionally substituted heterocyclic thio group; or R 3A and R 3B may together form an optionally substituted C 1-6 alkylidene group; or R 2A and R 3A may together form a group represented by the following formula [17]:
—O—Y 1 —O—  [17]

(wherein Y 1 represents an optionally substituted C 1-6 alkylene group or an optionally substituted siloxane group; and the bond on the left side binds to a carbon atom binding to R 2A ), or a bond; and X represents a leaving group), to react with a hydrogen sulfide or a salt thereof.

3. The production method according to claim 1 , wherein
R 1A and R 1B , which are the same or different, each represent a hydrogen atom, an optionally protected carboxyl group, an optionally substituted C 1-6 alkyl group or an optionally substituted aryl group; R 2A and R 2B , which are the same or different, each represent a hydrogen atom, a group represented by the following formula [15]:
—OR 2a   [15]

(wherein R 2a represents a hydroxyl-protecting group), or an optionally substituted aryl group; R 3A and R 3B , which are the same or different, each represent a hydrogen atom, a halogen atom, an optionally protected amino group, a group represented by the following formula [16]:
—OR 3a   [16]

(wherein R 3a represents a hydroxyl-protecting group), an optionally substituted C 1-6 alkyl group, an optionally substituted C 1-6 alkylthio group, an optionally substituted aryloxy group, an optionally substituted arylthio group or an optionally substituted heterocyclic thio group; or R 2A and R 3A may together form a group represented by the following formula [17]:
—O—Y 1 —O—  [17]

(wherein Y 1 represents an optionally substituted C 1-6 alkylene group or an optionally substituted siloxane group; and the bond on the left side binds to a carbon atom binding to R 2A ), or a bond.

4. The production method according to claim 1 , wherein
R 1A and R 1B , which are the same or different, each represent a hydrogen atom, a methyl group or a group represented by the following formula [18]:
—CH 2 OR

Assignees

• Fujifilm Corp

Inventors

• Nakamura Kouki
• Shimamura Satoshi
• Imoto Junichi
• TAKAHASHI Motomasa
• Watanabe Katsuyuki
• Wada Kenji
• FUJINO Yuuta
• Matsumoto Takuya
• Takahashi Makoto
• Okada Hideki
• Yamane Takehiro
• Ito Takayuki

Classifications

• A61P35/00

  Antineoplastic agents · CPC title

• C07C69/618

  having unsaturation outside the six-membered aromatic ring · CPC title

• C07C67/29 Primary

  by introduction of oxygen-containing functional groups · CPC title

• C07C47/19 Primary

  containing hydroxy groups (sugars C07H) · CPC title

• C07H13/08

  having the esterifying carboxyl radicals directly attached to carbocyclic rings · CPC title