Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701515Generated: October 31, 2026

N-(2-benzoyl-4-chlorophenyl)-methyl-hydrazinecarbothioamide → 7-Chloro-3-methyl-5-phenyl-2-thioxo-1,2-dihydro-3H-1,3,4-benzotriazepine

https://huagongshe.com/reaction/1701515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-benzoyl-4-chlorophenyl)-methyl-hydrazinecarbothioamideHCID 13972523—
Solvent1-PropanolHCID 1031—
Product7-Chloro-3-methyl-5-phenyl-2-thioxo-1,2-dihydro-3H-1,3,4-benzotriazepineHCID 135577924—

Reaction Steps

A mixture containing 20.0 grams of N-(2-benzoyl-4-chlorophenyl)-methyl-hydrazine-carbothioamide (Example 2) in 250 ml of n-propanol was refluxed for about 2 hours. The yellow precipitate was cooled in an ice bath, and the resulting yellow precipitate was collected, washed with isopropanol and air dried to yield 7-chloro-1,3-dihydro-3-methyl-5-phenyl-2H-1,3,4-benzotriazepine-2-thione as a yellow solid. Additional product was obtained upon evaporation of the solvent under vacuum. The melting point was found to be 188°-190° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04194000
Source datasetuspto-grants-1980_03
ORD IDord-50548de269774762a6ab082e3c14b080
Source noteuspto-grants-1980_03