Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328383Generated: October 27, 2026

7-chloro-2-[(1-carboxyethylidene)hydrazino]-5-phenyl-3H-1,4-benzodiazepine → 7-Chloro-2-[[1-(methoxycarbonyl)ethylidene]-hydrazino]-5-phenyl-3H-1,4-benzodiazepine

https://huagongshe.com/reaction/328383

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-chloro-2-[(1-carboxyethylidene)hydrazino]-5-phenyl-3H-1,4-benzodiazepineHCID 54054180—
ReactantHCID 178486252HCID 178486252—
SolventDiethyl EtherHCID 3283—
SolventChloroformHCID 6212—
SolventPentaneHCID 8003—
Product7-Chloro-2-[[1-(methoxycarbonyl)ethylidene]-hydrazino]-5-phenyl-3H-1,4-benzodiazepineHCID 53729966—

Reaction Steps

To a solution of 0.39 g. (0.001 mole) of 7-chloro-2-[(1-carboxyethylidene)hydrazino]-5-phenyl-3H-1,4-benzodiazepine is added 0.164 g. (0.0011 mole) of 3-methyl-1-p-tolyltriazene. After standing at room temperature (22°-25° C.) overnight, the solution is concentrated, then diluted with ether, filtered and evaporated to give a solid. This solid is redissolved in chloroform, diluted with ether and pentane to give .17 g. of 7-chloro-2-[[1-(merhoxycarbonyl)ethylidene]hydrazino]-5-phenyl-3H-1,4-benzodiazepine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04017492
Source datasetuspto-grants-1977_04
ORD IDord-ad87f8689b7e4c73b86ac5021a167049
Source noteuspto-grants-1977_04