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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389436Generated: October 31, 2026

Diazomethane → HCID 73165016, compound

https://huagongshe.com/reaction/1389436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 178526918HCID 178526918—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 73165016HCID 73165016—

Reaction Steps

A solution of diazomethane in ether was added to a suspension of 3.8 g (0.01 mol) of 7-chloro-5-(2-fluorophenyl)-N-hydroxy-α-nitro-3H-1,4-benzodiazepine-2-methanimine 4-oxide in 200 ml of methylene chloride. The mixture was stirred for 1 hr at room temperature whereby a clear solution resulted. The excess diazomethane was destroyed by addition of acetic acid. The reaction mixture was washed with aqueous sodium bicarbonate solution, dried over sodium sulfate and evaporated. Crystallization of the residue from ether yielded yellow crystals. The analytical sample was recrystallized from ether, mp 207°-209°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04244868
Source datasetuspto-grants-1981_01
ORD IDord-9fb8c57727f941f4ac67d2688943eed9
Source noteuspto-grants-1981_01