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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328387Generated: October 30, 2026

Diazomethane → HCID 53755453, compound

https://huagongshe.com/reaction/328387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
ReactantHCID 53749252HCID 53749252—
SolventDichloromethaneHCID 6344—
ProductHCID 53755453HCID 53755453—

Reaction Steps

A solution of 7-chloro-2-[[1-carboxy-4-(diethylamino)butylidene]hydrazino]-5-phenyl-3H-1,4-benzodiazepine in CH2Cl2 (10 ml.) is treated with stirring under N2, with an ethereal solution of diazomethane (5 ml., 0.3 M). After 1/2 hour the solution is concentrated in vacuo giving 7-chloro-2-[[1-(methoxycarbonyl)-4-(diethylamino)-butylidene]hydrazino]-5-phenyl-3H-1,4-benzodiazepine as an oil, the nmr of which confirmed the structure. Nmr (CDCl3) δ 0.95 (t, 3, CH2CH3) 1.82 (m, 2, CH2CH2CH2); 2.50 (m, 6, CH2CH3 and CH2CH2N), 2.27 (m, z, CCH2CH2), 3.77 (s, 3, OCH3), 4.50 (broad s, z, 3--CH2), between 6.80 and 7.85 (m, 8, arom H's).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04017492
Source datasetuspto-grants-1977_04
ORD IDord-a7e8d1b3ceb3499d9d66fdf215b5c650
Source noteuspto-grants-1977_04