CN106117206A - The synthetic method of medicine intermediate 4-trifluoromethyl guanine - Google Patents

The synthetic method of medicine intermediate 4-trifluoromethyl guanine Download PDF

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Publication number
CN106117206A
CN106117206A CN201510761457.9A CN201510761457A CN106117206A CN 106117206 A CN106117206 A CN 106117206A CN 201510761457 A CN201510761457 A CN 201510761457A CN 106117206 A CN106117206 A CN 106117206A
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CN
China
Prior art keywords
guanine
synthetic method
trifluoromethyl
medicine intermediate
trifluoromethyl guanine
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Pending
Application number
CN201510761457.9A
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Chinese (zh)
Inventor
彭海燕
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
WUXI QIANHAO BIO-PHARMACEUTICAL Co Ltd
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WUXI QIANHAO BIO-PHARMACEUTICAL Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Priority to CN201510761457.9A priority Critical patent/CN106117206A/en
Publication of CN106117206A publication Critical patent/CN106117206A/en
Pending legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/18Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

The present invention relates to the synthetic method of a kind of medicine intermediate 4-trifluoromethyl guanine, with guanine as raw material, under the effect of solvent methanol and acetone, at 1.6 atmospheric pressure, temperature 120 DEG C-150 DEG C, first pass through displacement method react with fluoride, then by the generation 4-trifluoromethyl guanine that methylates.The synthetic method of medicine intermediate 4-trifluoromethyl guanine of the present invention is simple, efficient, and operates safety, very useful in concrete production.

Description

The synthetic method of medicine intermediate 4-trifluoromethyl guanine
Technical field
The present invention relates to the synthetic method of a kind of medicine intermediate 4-trifluoromethyl guanine.
Background technology
4-trifluoromethyl guanine is the initiation material of many pharmaceutical synthesis, the important intermediate of particularly a lot of guanine compounds, the most domestic synthetic method having no this compound of report.
Summary of the invention
It is an object of the invention to overcome above-mentioned deficiency, it is provided that a kind of simple, efficiently, the synthetic method of the medicine intermediate 4-trifluoromethyl guanine of safety operation.
The object of the present invention is achieved like this:
A kind of synthetic method of medicine intermediate 4-trifluoromethyl guanine, with guanine as raw material, under the effect of solvent methanol and acetone, at 1.6 atmospheric pressure, temperature 120 DEG C-150 DEG C, first pass through displacement method react with fluoride, then by the generation 4-trifluoromethyl guanine that methylates.
Compared with prior art, the invention has the beneficial effects as follows:
The synthetic method of medicine intermediate 4-trifluoromethyl guanine of the present invention is simple, efficient, and operates safety, very useful in concrete production.
Detailed description of the invention
The synthetic method of medicine intermediate 4-trifluoromethyl guanine of the present invention is specific as follows:
With guanine as raw material, under the effect of solvent methanol and acetone, at 1.6 atmospheric pressure, temperature 120 DEG C-150 DEG C, first pass through displacement method react with fluoride, then by the generation 4-trifluoromethyl guanine that methylates.The purity of this crude product can meet general reaction requirement, can direct plunge in reaction.

Claims (1)

1. the synthetic method of a medicine intermediate 4-trifluoromethyl guanine, it is characterized in that with guanine as raw material, under the effect of solvent methanol and acetone, at 1.6 atmospheric pressure, temperature 120 DEG C-150 DEG C, first pass through displacement method react with fluoride, then by the generation 4-trifluoromethyl guanine that methylates.
CN201510761457.9A 2015-11-11 2015-11-11 The synthetic method of medicine intermediate 4-trifluoromethyl guanine Pending CN106117206A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510761457.9A CN106117206A (en) 2015-11-11 2015-11-11 The synthetic method of medicine intermediate 4-trifluoromethyl guanine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510761457.9A CN106117206A (en) 2015-11-11 2015-11-11 The synthetic method of medicine intermediate 4-trifluoromethyl guanine

Publications (1)

Publication Number Publication Date
CN106117206A true CN106117206A (en) 2016-11-16

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510761457.9A Pending CN106117206A (en) 2015-11-11 2015-11-11 The synthetic method of medicine intermediate 4-trifluoromethyl guanine

Country Status (1)

Country Link
CN (1) CN106117206A (en)

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C06 Publication
PB01 Publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20161116

WD01 Invention patent application deemed withdrawn after publication