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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698956Generated: November 2, 2026

Triethylamine → HCID 178527248, compound

https://huagongshe.com/reaction/1698956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanesulfonylchloride, 2-chloro-HCID 15385—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178527248HCID 17852724854%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred solution of 6-amino-4-[(3-bromophenyl)amino]quinazoline (J Med Chem, 1995;38:3482) (0.30 g, 0.95 mmol) in THF (20 mL) under nitrogen was added Et3N (3.5 mol eq., 3.33 mmol, 245 μL), a catalytic amount of DMAP and chloroethanesulfonyl chloride (1.2 mol eq., 1.14 mmol, 119 μL) dropwise. The reaction was stirred at 25° C. for 1 hour and then diluted with saturated NaHCO3 and extracted with EtOAc. The combined organic extracts were washed with brine, dried over anhydrous Na2SO4, concentrated under reduced pressure, and chromatographed on silica gel eluting with MeOH/CH2Cl2/EtOAc (3:47:50). Crystallization from CH2Cl2/hexane gave N-[4-[(3-bromophenyl)amino]quinazolin-6-yl]vinylsulfonamide (210 mg, 54%) as a cream powder, mp 217° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06344459B1
Source datasetuspto-grants-2002_02
ORD IDord-b43b553841824300a309324ac43c43cf
Source noteuspto-grants-2002_02