IP Library Granted Patent US 7,339,054
Granted Patent B2
US 7,339,054 · App. 10/544,575 · Granted Mar 4, 2008

Process for preparing branched ribonucleosides from 1,2-anhydroribofuranose intermediates

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,339,054
App. No.
10/544,575
Granted
Mar 4, 2008
Kind
B2
Abstract

A process is provided for the preparation of branched-chain ribonucleosides of formula (I): from the 1,2-anhydroderivatives of formula (II). wherein PG is a hydroxyl protecting group, B is a purine or pyrimidine nucleobase, and R 1 is C 1-6 alkyl. The compounds of formula (I) are inhibitors of HCV polymerase useful in the treatment of HCV infection.

Claims (34)

1. A process for preparing a compound of structural formula I:

wherein R 1 is C 1-6 alkyl and B is a purine or pyrimidine nucleobase selected from the group consisting of cytosine, uracil, thymine, hypoxanthine, adenine, guanine, 7-deazaguanine, 7-deazaadenine, 7-deaza-2,6-diaminopurine, and 7-deazahypoxanthine;

comprising the steps of

(a) producing a compound of structural formula IV:

 wherein B′ is optionally protected B,

 by contacting a compound of structural formula II:

 wherein PG is a hydroxyl protecting group,

 with a nucleophile B′ in a suitable organic solvent; and

(b) removing the hydroxyl protecting groups PG and optional protecting groups in B′.

2. The process of claim 1 additionally comprising the step of producing a compound of structural formula II:

by treating a compound of structural formula III:

with a sulfonylating or halogenating agent in a suitable organic solvent in the presence of base, wherein said base is added before, during, or after said treatment with said sulfonylating or halogenating agent.

3. The process of claim 1 wherein B is guanine, cytosine, adenine, or 7-deazaadenine.

4. The process of claim 3 wherein B is 7-deazaadenine.

5. The process of claim 1 wherein R 1 is methyl.

6. The process of claim 4 wherein R 1 is methyl.

7. The process of claim 1 wherein said hydroxyl protecting group is an ester, silyl ether, or optionally substituted benzyl ether protecting group.

8. The process of claim 7 wherein said hydroxyl protecting group is an ester protecting group.

9. The process of claim 8 wherein said ester protecting group is a benzoate ester unsubstituted or substituted with one to two groups independently selected from halogen, cyano, methoxy, nitro, and methyl.

10. The process of claim 2 wherein the compound of structural formula II is produced by treating a compound of structural formula III with a sulfonylating agent in a suitable organic solvent in the presence of base.

11. The process of claim 10 wherein said sulfonylating agent is methanesulfonyl chloride.

12. The process of claim 10 wherein said base is an amine base selected from the group consisting of triethylamine, pyridine, 4-(dimethylamino)pyridine, N,N-diisopropylethylamine, and diisopropylamine.

13. A process for preparing a compound of structural formula I:

wherein R 1 is C 1-6 alkyl and B is a purine or pyrimidine nucleobase selected from the group consisting of cytosine, uracil, thymine, hypoxanthine, adenine, guanine, 7-deazaguanine, 7-deazaadenine, 7-deaza-2,6-diaminopurine, and 7-deazahypoxanthine;

comprising the steps of:

(a) producing a compound of structural formula (II)

 wherein PG is a hydroxyl protecting group,

 by treating a compound of structural formula III:

 with a sulfonylating or halogenating agent in a suitable organic solvent in the presence of base, wherein said base is added before, during, or after treatment with said sulfonylating or halogenating agent;

(b) producing a compound of structural formula IV:

 wherein B′ is optionally protected B,

 by contacting a compound of structural formula II:

 with a nucleophile B′ in a suitable organic solvent; and

(c) removing the hydroxyl protecting groups PG and optional protecting groups in B′.

Assignments (4)
CHANGE OF NAME Recorded Aug 29, 2012
From: SCHERING CORPORATION
To: MERCK SHARP & DOHME CORP.
Reel/Frame 028866/0511 →
MERGER Recorded Aug 27, 2012
From: MERCK SHARP & DOHME CORP.
To: SCHERING CORPORATION
Reel/Frame 028850/0515 →
CHANGE OF NAME Recorded Jan 29, 2010
From: MERCK & CO., INC.
To: MERCK SHARP & DOHME CORP.
Reel/Frame 023861/0910 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2007
From: XU, FENG; BIO, MATTHEW M.; COWDEN, CAMERON J.; SAVARY, KIMBERLY A.; WILLIAMS, JOHN M.; YANG, CHUNHUA; WATERS, MARJORIE SEE
To: MERCK & CO., INC.
Reel/Frame 019180/0083 →