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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069023Generated: October 30, 2026

Triethylamine → HCID 5329094, compound

https://huagongshe.com/reaction/1069023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanesulfonylchloride, 2-chloro-HCID 15385—
ReactantN4-(3-Bromophenyl)quinazoline-4,6-diamineHCID 5328042—
SolventTetrahydrofuranHCID 8028—
ProductHCID 5329094HCID 532909452.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-(3-bromophenyl)-4,6-quinazolindiamine (315 mg, 1 mmol) and triethylamine (0.5 mL) in THF (50 mL) at 0° C. was dropwise added 2-chloroethylsulfonyl chloride (490 mg, 3 mmol). After the solution was stirred at 0° C. for 10 min, it was chromatographed on silica gel with 10% methanol in chloroform to give 212 mg of ethenesulfonic acid [4-(3-bromo-phenylamino)-quinazolin-6-yl]-amide as an light yellow solid: HRMS (m/e): M+403.9937. Modified a method from A. A. Goldberg, J. Chem., Soc., 464 (1945).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251912B1
Source datasetuspto-grants-2001_06
ORD IDord-4e243c6ee6004e5b992880e7f70e317d
Source noteuspto-grants-2001_06