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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069007Generated: October 27, 2026

N,N-Diisopropylmethylamine → 4-Methoxy-but-2-enoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide

https://huagongshe.com/reaction/1069007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DiisopropylmethylamineHCID 547370—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
Reactant4-Methoxycrotonyl chlorideHCID 22466554—
ReactantSodium hydrogencarbonate brineHCID 129703874—
SolventTetrahydrofuranHCID 8028—
Product4-Methoxy-but-2-enoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amideHCID 5439194695.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 1.0 g of N-(3-bromophenyl)-4,6-quinazolindiamine and 0.62 g of diisopropyl methylamine in 21 mL of tetrahydrofuran at 0° C. was added 0.62 g of 4-methoxycrotonyl chloride. The mixture was stirred at 0° C. for 1.5 hr and 10 min at room temperature. The mixture was poured into saturated sodium bicarbonate-brine and extracted with ethyl acetate. The organic solution was dried over magnesium sulfate. The solution was filtered through silica gel and the solvent was removed. The residue was recrystallized from 1-butanol to give 1.25 g of 4-Methoxy-but-2-enoic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide as a yellow solid: mass spectrum (m/e): M+H 415.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251912B1
Source datasetuspto-grants-2001_06
ORD IDord-140e71bc53c54d56aec6bd1923a12126
Source noteuspto-grants-2001_06