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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732204Generated: November 2, 2026

Acetohydrazide → HCID 20350618, compound

https://huagongshe.com/reaction/1732204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydrazideHCID 14039—
Reactant3H-1,3,4-Benzotriazepine, 7-chloro-3-methyl-2-(methylthio)-5-phenyl-HCID 628794—
Solvent1-ButanolHCID 263—
ProductHCID 20350618HCID 20350618—

Reaction Steps

A mixture of 7.25 grams (23.0 m moles) of 7-chloro-3-methyl-(methylthio)-5-phenyl-3H-1,3,4-benzotriazepine (Example 27), 4.8 grams (65 moles) of acethydrazide, and 100 ml of n-butanol was stirred and refluxed under nitrogen for about 17 hours. The solvent was removed in vacuo on a rotary evaporator. The residue was dissolved in methylene chloride. The resulting solution was washed with water, dried with magnesium sulfate, and concentrated in vacuo. The residue was dissolved in a minimum amount of warm carbon tetrachloride. The solution was cooled and seeded with product. The precipitate was collected, washed with cold carbon tetrachloride, and air dried to yield the title compound as a yellow solid. The melting point was found to be 224.5°-227.5° C. The structure was confirmed by elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237049
Source datasetuspto-grants-1980_12
ORD IDord-901a7290e59445c3aa60a9a605504f7b
Source noteuspto-grants-1980_12