戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 328381作成日:2026年10月26日

Methyl pyruvate → HCID 53751159、化合物

https://huagongshe.com/reaction/328381

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl pyruvateHCID 11748—
反応物7-Chloro-2-hydrazinyl-5-phenyl-3H-1,4-benzodiazepineHCID 12390874—
溶媒MethanolHCID 887—
生成物HCID 53751159HCID 53751159—

反応手順

A mixture of 5.7 g. (0.02 mole) of 7-chloro-2-hydrazino-5-phenyl-3H-1,4-benzodiazepine, 3 ml. (0.04 mole) of methyl pyruvate and 50 ml. of methanol is stirred, under nitrogen, for 17 hours at room temperature, by which time the solid has dissolved. Three ml. more methyl pyruvate is added and the solution is allowed to stand for 7 hours more. After filtration and evaporation in vacuo (50° C./0.5 mm.) a brown gum is obtained which is chromatographed on silica gel and eluted with 1% methanol in chloroform. Evaporation of the combined fractions containing the product (as indicated by thin layer chromatography) gives a gum which is crystallized from a mixture of chloroform and ether. A yield of 3.5 g. (67%) of 7-chloro-2-[[1-methoxycarbonyl)ethylidene]hydrazino]-5-phenyl-3H-1,4-benzodiazepine is obtained as nearly white crystals of melting point 156°-157° C. Melt solvate indicates the product contained 1.95% CHCl3 even after prolonged drying in vacuo.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04017492
出典データセットuspto-grants-1977_04
ORD IDord-e62459c7d01d41e2bcecb80f4214d39b
出典メモuspto-grants-1977_04