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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046606Generated: November 2, 2026

Phenylmethanesulfonyl chloride → HCID 59464684, compound

https://huagongshe.com/reaction/1046606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylmethanesulfonyl chlorideHCID 74740—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(4-Nitrophenyl)-1-(2-thiophene-2-ylthiazol-4-yl)ethylamineHCID 66705334—
SolventDichloromethaneHCID 6344—
ProductHCID 59464684HCID 59464684—

Reaction Steps

To a suspension of 2-(4-nitrophenyl)-1-(2-thiophene2-ylthiazol-4-yl)ethylamine, 8, (330 mg, 0.80 mmol) in CH2Cl2 (6 mL) at 0° C. is added diisopropylethylamine (0.30 mL, 1.6 mmol) followed by phenylmethanesulfonyl chloride (167 mg, 0.88 mmol). The reaction mixture is stirred at room temperature for 14 hours. The mixture is diluted with CH2Cl2 and washed with sat. NaHCO3 followed by brine, dried (Na2SO4), filtered and concentrated in vacuo. The resulting residue is purified over silica to afford 210 mg of the desired product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569348B2
Source datasetuspto-grants-2013_10
ORD IDord-96a57a978fb74b35a2bf4feabd0d9e91
Source noteuspto-grants-2013_10