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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786174Generated: November 1, 2026

2-Methoxyacetohydrazide → 9-Bromo-2-methoxymethyl-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one

https://huagongshe.com/reaction/1786174

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyacetohydrazideHCID 2759532—
ReactantEthyl (4-bromo-2-cyanophenyl)carbamateHCID 18367857—
Product9-Bromo-2-methoxymethyl-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-oneHCID 13633232892%

Reaction Steps

As described for example 1a) (4-bromo-2-cyano-phenyl)-carbamic acid ethyl ester (19.9 g, 74.2 mmol) instead of (4-chloro-2-cyano-phenyl)-carbamic acid ethyl ester using methoxymethyl-carboxylic acid hydrazide instead of cyclopropane-carboxylic acid hydrazide, was converted to the title compound (21.1 g, 92%) which was obtained as a light yellow solid. MS: m/e=308.9/310.9 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507729B2
Source datasetuspto-grants-2009_03
ORD IDord-10b35571eb37418eb7d2de4465667b0c
Source noteuspto-grants-2009_03