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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612018Generated: October 31, 2026

4-Methylmorpholine → HCID 22466694, compound

https://huagongshe.com/reaction/612018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
Reactant6-Amino-4-(3-bromophenylamino)quinoline-3-carbonitrileHCID 9967712—
Reactant4-{[tert-Butyl(dimethyl)silyl]oxy}but-2-ynoic acidHCID 22478445—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 22466694HCID 2246669435%

Reaction Steps

Isobutyl chloroformate(0.214 g, 1.57 mmol) and N-methylmorpholine(0.190 g, 1.88 mmol) were added to an ice cold solution of 0.336 g (1.57 mmol) of 4(tert-butyl-dimethyl-silanyloxy)-2-butynoic acid in 15 mL of tetrahydrofuran under N2. After stirring for 30 min, it was transferred to an additional funnel plugged with a glass wool and added dropwise to a solution of 0.4 g (1.18 mmol) of 6-amino-4-[(3-bromophenyl)amino]-3-quinolinecarbonitrile in 3 mL of tetrahydrofuran and 1.5 ml of pyridine. The mixture was stirred at 25° C. for 1 h. The reaction solution was poured into ethyl acetate and washed with saturated sodium bicarbonate and brine. The product was collected and purified by flash column chromatography (60% ethyl acetate in hexane) to give 0.220 g of N-[4-[(3-Bromophenyl)amino]-3-cyano-6-quinolinyl]-4-(tert-butyl-dimethyl-silanyloxy)-2-butynamide as a yellow solid (35%); ESMS m/z 535.1 (M+H+); mp ° C.(dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06002008
Source datasetuspto-grants-1999_12
ORD IDord-ecb073e83cbd4f8d9b70dec725248564
Source noteuspto-grants-1999_12