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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068975Generated: November 1, 2026

4-Methylmorpholine → HCID 5328961, compound

https://huagongshe.com/reaction/1068975

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant4-Morpholino-2-butynoic acidHCID 541908—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 5328961HCID 532896132.4%

Reaction Steps

Isobutyl chloroformate (0.343 g, 2.5 mmol) and N-methylmorpholine (0.322 g, 3.18 mmol) were added to an ice cold solution of 0.540 g (3.18 mmol) of 4-morpholin-4-yl-but-2-ynoic acid in 50 mL of tetrahydrofuran under nitrogen. After stirring for 30 min, a solution of 0.500 g of N-(3-bromophenyl)-4,6-quinazolindiamine in 10 mL of pyridine was added and the mixture was stirred at 0° C. for 2 hr. 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 0.240 g of 4-morpholin-4-yl-but-2-ynoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide: mass spectrum (m/e): M+H 466.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251912B1
Source datasetuspto-grants-2001_06
ORD IDord-fb5d98dba48b4b40a0aa44eb20fba78e
Source noteuspto-grants-2001_06