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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448962Generated: October 31, 2026

2-Chloro-6,7-dimethoxy-4-quinazolinamine → HCID 13723660, compound

https://huagongshe.com/reaction/1448962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-6,7-dimethoxy-4-quinazolinamineHCID 90235—
Reactant(2,3-Dihydro-1,4-benzodioxin-2-yl)(hexahydro-1H-1,4-diazepin-1-yl)methanoneHCID 13723686—
Solvent1-ButanolHCID 263—
ProductHCID 13723660HCID 1372366017.2%

Reaction Steps

4-Amino-2-chloro-6,7-dimethoxyquinazoline (1.58 g.) and N-(1,4-benzodioxan-2-carbonyl)homopiperazine (2.0 g.) were heated under reflux in n-butanol (114 ml.) for 60 hours. The mixture was then cooled, butanol removed in vacuo and the solid residue triturated with ether, taken up in hot methanol, filtered and cooled. The solid product was collected, then the residual solution was evaporated in vacuo and the residue taken up in hot isopropanol, cooled, filtered, then re-evaporated in vacuo. The residue was combined with the original solid product, treated with cold methanol, and recrystallized from ethanol to give 4-amino-2-[4-(1,4-benzodioxan-2-carbonyl)homopiperazin-1-yl]-6,7-dimethoxyquinazoline hydrochloride (0.57 g.), m.p. 250°-251° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04188390
Source datasetuspto-grants-1980_02
ORD IDord-7e753f9957b1465d8a0e64281c8e7269
Source noteuspto-grants-1980_02