The present invention provides a method for producing an inosine derivative represented by the following general formula (1) including the steps of subjecting an inosine derivative of general formula (3) to dithiocarbonylation and carrying out radical reduction of the obtained compound. According to the present invention there can be produced compounds useful as anti-AIDS drugs on industrial scale. [structure] wherein R1 may be the same or different and are each benzyl group, benzhydryl group or trityl group, each of which may have a substituent in general formulas (1) and (3).

Claims

6 · 2 independent · depth 2

6 granted claims

›1.independentA method for producing an inosine compound represented by formula (1):+2

›4.independentA method for producing an inosine compound represented by formula (2):+2

Classifications

8 codes

IPC · International Patent Classification

Section C — Chemistry; metallurgy

C07H19/16
C07H19/167
C07H19/173

USPC · US Patent Classification

536/27.8536/27.21544/265514/45536/27.1

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File wrapper

Pendency

2.1 y

760 days filing → grant

Office actions

non-final + final

Responses

no RCE

Examiner

Shaojia Anna Jiang

art unit 1623 · TC 1600

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Citations: 12 back · 0 forward

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Priority chain

1 priority documents

›Priority documents — 1

Type	Document	Date
related publication	US 20110028706 A1	3 Feb 2011

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