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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068977Generated: October 31, 2026

4-Methylmorpholine → HCID 5328965, compound

https://huagongshe.com/reaction/1068977

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
Reactant2-Butynoic acid, 4-methoxy-HCID 11126213—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 5328965HCID 532896541.4%

Reaction Steps

Isobutyl chloroformate (0.432 g, 3.2 mmol) and N-methylmorpholine (0.959 g, 9.48 mmol) were added to an ice cold solution of 0.720 g (6.32 mmol) of 4-methoxy-but-2-ynoic acid in 30 mL of tetrahydrofuran under nitrogen. After stirring for 30 min, a solution of 0.500 g of N-(3-bromophenyl)-4,6-quinazolindiamine in 8 mL of pyridine was added and the mixture was stirred for 2 hr at 0° C. The reaction was then quenched with ice water, poured into saturated sodium bicarbonate, and the product was extracted with ethyl acetate. Chromatography of the extract on silica gel, eluting with methanol/ethyl acetate (15:85), gave 0.270 g of 4-Methoxy-but-2-ynoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide: mass spectrum (m/e): M+H 411.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251912B1
Source datasetuspto-grants-2001_06
ORD IDord-3a220d51dbcd4a88a98639b0e79c9a4c
Source noteuspto-grants-2001_06