Method for preparing 42-(dimethylphosphinate) rapamycin

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United States of America Patent

PATENT NO 8722880
SERIAL NO

13967597

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Abstract

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A method for preparing 42-(dimethylphosphinate) Rapamycin (Ridaforolimus) (I) is provided, which has advantages of high conversion rate and no 31,42-bis(dimethyl phosphinate) Rapamycin (III) generated. In the method of the present invention, Rapamycin (II) is firstly reacted with triethyl chlorosilane in a base condition to form 31,42-bis(triethylsilylether) Rapamycin (IV-b), followed by a selective deprotection process to obtain 31-triethylsilylether Rapamycin (V-b). Next, a phosphorylation reaction is performed by using dimethylphosphinic chloride under a base solution to obtain a crude product. Finally, a deprotection reaction is performed in a diluted sulfuric acid solution to obtain a crude product of Ridaforolimus (I). Since the conversion rate of each step of the method of the present invention is higher than 98%, it indicates that the method of the present invention is suitable for industrial production.

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Patent Owner(s)

Patent OwnerAddress
CHUNGHWA CHEMICAL SYNTHESIS & BIOTECH CO LTDNO 1 DONGXING ST SHULIN DIST NEW TAIPEI CITY 238

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Inventor(s)

Inventor Name Address # of filed Patents Total Citations
Lee, Kwang-Chung New Taipei, TW 6 28
Lee, Tzu-Ai New Taipei, TW 4 17
Shih, Yu-Hsuan New Taipei, TW 2 0
Tung, Yen-Shih New Taipei, TW 5 44

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