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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069005Generated: October 29, 2026

4-Methylmorpholine → HCID 5328967, compound

https://huagongshe.com/reaction/1069005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantSodium BicarbonateHCID 516892—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
ReactantHCID 10942555HCID 10942555—
SolventTetrahydrofuranHCID 8028—
ProductHCID 5328967HCID 5328967—

Reaction Steps

To a stirred solution of 0.66 g of 4-methoxymethoxy-but-2-ynoic acid and 0.60 mL of isobutyl chloroformate in 16 mL of tetrahydrofuran at 0° C. was added 0.5 mL of N-methylmorpholine followed by 1.2 g of solid N-(3-bromophenyl)-4,6-quinazolindiamine. Stirring was continued for 1 hr at 0° C. and 30 min at room temperature. Another equal amount of mixed anhydride as prepared above was added. The mixture was stirred an addition 30 min and stored at −10° C. over night. The mixture was poured into saturated sodium bicarbonate and extracted with ethyl acetate. The organic solution was dried over magnesium sulfate. The solvent was removed and the residue was chromatographed on silica gel eluting with ethyl acetate and choroform solvent mixtures to give 0.35 g of 4-Methoxymethoxy-but-2-ynoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide as a tan solid: mass spectrum (m/e): M+H 441.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251912B1
Source datasetuspto-grants-2001_06
ORD IDord-bb383e02f4e143ffa90749df7bbd1a0f
Source noteuspto-grants-2001_06