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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972092Generated: October 29, 2026

Acetohydrazide → HCID 20350618, compound

https://huagongshe.com/reaction/972092

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 225.5°-227.5° C. The structure was confirmed by elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04163104
Source datasetuspto-grants-1979_07
ORD IDord-cbc504c41adb446d9f1b10e64dd1a9f5
Source noteuspto-grants-1979_07