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【结 构 式】

【分子编号】15167

【品名】methyl 2-diazoacetate

【CA登记号】

【 分 子 式 】C3H4N2O2

【 分 子 量 】100.07704

【元素组成】C 36.01% H 4.03% N 27.99% O 31.97%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(XXIX)

The chiral intermediate (1R,2S)-N-(tert-butoxycarbonyl)-2-fluorocyclopropylamine (III) can also be obtained as follows: 4) The cyclopropanation of 1-chloro-1-fluoroethylene (XXVIII) with diazoacetic esters (XXIX) catalyzed by rhodium catalysts, especially dirhodium (II) tetrakistriphenylacetate, gives preferentially the corresponding 2t-chloro-2c-fluorocyclopropane-1r-carboxylic esters (XXX), which are easily dechlorinated to the cis-racemic-2-fluorocyclopropanecarboxylic acid (XII), already obtained as intermediate in the synthesis shown in Scheme 2.

1 Castaner, J.; Graul, A.; Prous, J.; DU-6859. Drugs Fut 1994, 19, 9, 827.
2 Kohda, H.; Takahashi, H.; Ishida, Y.; et al.; Practical synthesis of DU-6859a: Novel synthesis of cis-2-fluorocyclopropanecarboxylic acid, the key intermediate of 1-substituent. 33rd Intersci Conf Antimicrob Agents Chemother (Oct 17-20, New Orleans) 1993, Abst 975.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XII) 15136 rac-(2-fluorocyclopropanecarboxylic acid) C4H5FO2 详情 详情
(XXVIII) 15166 1-chloro-1-fluoroethylene 2317-91-1 C2H2ClF 详情 详情
(XXIX) 15167 methyl 2-diazoacetate C3H4N2O2 详情 详情
(XXX) 15168 methyl 2-chloro-2-fluorocyclopropanecarboxylate C5H6ClFO2 详情 详情
Extended Information