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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068984Generated: November 1, 2026

4-Methylmorpholine → HCID 10164583, compound

https://huagongshe.com/reaction/1068984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
ReactantHCID 18548945HCID 18548945—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10164583HCID 1016458327.1%

Reaction Steps

Isobutyl chloroformate (0.845 g, 6.2 mmol) and N-methylmorpholine (0.963 g, 9.52 mmol) were added to an ice cold solution of 2.100 g (9.52 mmol) of 4-[bis-(2-methoxy-ethyl)-amino]-but-2-ynoic acid in 50 mL of tetrahydrofuran under nitrogen. After stirring for 30 min, a solution of 1.500 g of N-(3-bromophenyl)-4,6-quinazolindiamine in 10 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 0.660 g of 4-[Bis-(2-methoxy-ethyl)-amino]-but-2-ynoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide: mass spectrum (m/e): M+H 512.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251912B1
Source datasetuspto-grants-2001_06
ORD IDord-12cb9f05de374efaa62a6b5d8f3e8661
Source noteuspto-grants-2001_06