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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059126Generated: November 3, 2026

Hydrochloric Acid → HCID 15587237, compound

https://huagongshe.com/reaction/2059126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 13500511HCID 13500511—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 15587237HCID 15587237—

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 10.37 g (28.9 mmoles) of 2-(1-ethylacetonyl)-4,5-dimethoxy-2'-chlorobenzophenone, 10.5 ml of glacial acetic acid and 2.65 ml of concentrated hydrochloric acid is heated to 95° C. under stirring. The mixture is cooled to 60° C., and 2.14 ml of 98% hydrazine hydrate are added to the mixture in portions, whereupon the temperature of the mixture raises to 85° C. After 30 minutes a solution of 1.44 g of sodium hydroxide in 4.5 ml of water is added to the mixture, followed by 10 ml of methanol. The resulting solution is poured into 130 ml of water, and the separated 5H-2,3-benzodiazepine derivative is isolated. 9.04 g (88%) of the title compound are obtained; m.p.: 129°-131° C. C20H21ClN2O2 =356.9. The crude product can be recrystallized e.g. from ethanol. The product with the highest purity grade melts at 147°-149° C. The rhodanide salt of the title compound ([C20H22ClN2O2 ]SCN=425.95) melts at 169°-171° C. after recrystallization from isopropanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04322346
Source datasetuspto-grants-1982_03
ORD IDord-2c60d4efde064c8587f3b70fcb7f8726
Source noteuspto-grants-1982_03