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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103623Generated: October 31, 2026

p-Bromobenzenesulfonyl chloride → 4-bromo-N-(2-pyridin-2-ylethyl)benzenesulfonamide

https://huagongshe.com/reaction/2103623

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
ReactantTriethylamineHCID 8471—
Reactant2-PyridineethanamineHCID 75919—
ReactantSodium BicarbonateHCID 516892—
SolventDichloromethaneHCID 6344—
Product4-bromo-N-(2-pyridin-2-ylethyl)benzenesulfonamideHCID 352704497.9%

Reaction Steps

Add a solution of 4-bromo-benzenesulfonyl chloride (1.278 g, 5.0 mmol) in 10 mL dichloromethane at r.t. to a solution of 2-pyridin-2-yl-ethylamine (611 mg, 5.0 mmol) and triethylamine (708 μL, 5.0 mmol) in 5 mL dichloromethane over a period of 20 min via syringe pump and stir for 12 h. Add 20 mL saturated aqueous sodium bicarbonate solution and extract the aqueous phase with dichloromethane. Wash the combined organic extracts with brine, dry over sodium sulfate, filtrate and concentrate under reduced pressure to obtain 4-bromo-N-(2-pyridin-2-yl-ethyl)-benzenesulfonamide (1.67 g) as a pale yellow oil which slowly crystallizes upon storage at ambient temperature. Further purification is not necessary. MS (m/e): 342 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576108B2
Source datasetuspto-grants-2009_08
ORD IDord-b2b1625b0c904ba4bb4cd2594d858549
Source noteuspto-grants-2009_08