Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764538Generated: October 31, 2026

Water → 7-Chloro-2-hydrazinyl-5-phenyl-3H-1,4-benzodiazepine

https://huagongshe.com/reaction/1764538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 22768401HCID 22768401—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product7-Chloro-2-hydrazinyl-5-phenyl-3H-1,4-benzodiazepineHCID 12390874—

Reaction Steps

Thus obtained 2-benzylmercapto-7-chloro-5-phenyl-3H-1,4-benzodiazepine (4 parts) is dissolved in 100 parts by volume of a mixture of methanol and tetrahydrofuran (1:1) and 10 parts by volume of hydrazine hydrate is added thereto. After being left standing overnight at room temperature, the reaction mixture is poured into water and extracted with chloroform. The chloroform layer is washed with water and dried over sodium sulfate. Evaporation of the solvent affords 7-chloro-2-hydrazino-5-phenyl-3H-1,4-benzodiazepine. Recrystallization from a mixture of chloroform and benzene gives colorless crystals. M.P. 203°-205° C (decomposition). Thus obtained product is identical with the product prepared in Examples 1 and 9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04116956
Source datasetuspto-grants-1978_09
ORD IDord-db496511f23b47e189c1b9929967281b
Source noteuspto-grants-1978_09