Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464041Generated: October 29, 2026

4-Chloro-6,7-dimethoxyquinazoline → HCID 20263805, compound

https://huagongshe.com/reaction/464041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—
ReactantN-ButylhydrazinecarboxamideHCID 12676228—
Solvent1-PentanolHCID 6276—
ProductHCID 20263805HCID 20263805—
ProductHCID 70068045HCID 70068045—

Reaction Steps

3 g of 6,7-dimethoxy-4-chloro-quinazoline were stirred with 3.5 g of 4-n-butyl-semicarbazide in 100 ml of n-amyl alcohol for 2 hours at 100° C. Then, the precipitate which had formed was suction-filtered off, suspended while in hot ethanol and brought to pH 5 by the addition of 2N hydrochloric acid. The clear solution was filtered through charcoal, cooled, suction-filtered and dried in a circulating air drier. The hydrochloride of 4-n-butyl-4-(6,7-dimethoxyquinazol-4-yl)-semi-carbazide, which was obtained with a 70% yield, melted at 216°-217° C. The following compounds were obtained analogously.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04546102
Source datasetuspto-grants-1985_10
ORD IDord-c31210b9febb4032a445c76e0a168707
Source noteuspto-grants-1985_10