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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26052Generated: October 29, 2026

Chloroform → HCID 20394584, compound

https://huagongshe.com/reaction/26052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantAmmonium HydroxideHCID 14923—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantHCID 20394577HCID 20394577—
SolventDichloromethaneHCID 6344—
ProductHCID 20394584HCID 20394584—

Reaction Steps

A stirred suspension of 3 g (0.0075 mole) of 8-chloro-6-(2-chlorophenyl)-1,2-dihydro-2-methyl-1-oxo-4H-imidazo[1,5-a][1,4]benzodiazepin-3-carboxylic acid in 90 ml of methylene chloride was cooled in an ice bath and treated with 1.9 g (0.009 mole) of phosphorus pentachloride in portions. Stirring in the cold under a drying tube was continued for 30 min. Ammonia was then bubbled into the cold solution for 5 min and stirring in the cold was continued 30 min. longer. Evaporation at reduced pressure gave a tan solid. The solid was stirred with 3N ammonium hydroxide and extracted with methylene chloride. An emulsion formed but was destroyed by filtering to remove some high melting solid. The methylene chloride layer was dried over sodium sulfate and evaporated to give a yellow solid which was recrystallized from benzene to give off-white needles with mp 158°-160°. Uv λ sh 215 mμ (ε=43000) max 272 (15500) sh 330 (2500); ir (CHCl3) 3510, 3400 cm-1 (NH2) 1703 (CO) 1685 (CONH2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04147875
Source datasetuspto-grants-1979_04
ORD IDord-84a0c15c4b624da08da56af5f4e583b0
Source noteuspto-grants-1979_04