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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363111Generated: November 4, 2026

Pyridine → (S)-N-(1-Benzoyl-6-cyano-1,2,3,4-tetrahydroquinolin-3-yl)-benzene-sulfonamide

https://huagongshe.com/reaction/1363111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
Reactant(S)-N-(6-Cyano-1,2,3,4-tetrahydro-quinolin-3-yl)-benzenesulfonamideHCID 66757946—
SolventDichloromethaneHCID 6344—
Product(S)-N-(1-Benzoyl-6-cyano-1,2,3,4-tetrahydroquinolin-3-yl)-benzene-sulfonamideHCID 6675816888%

Reaction Steps

To a solution of 1G (62 mg, 0.2 mmol) in CH2Cl2 (1 mL) was added pyridine (0.049 mL, 0.6 mmol), followed by addition of benzoyl chloride (42 mg, 0.3 mmol). The resulting mixture was stirred at RT under argon for 6 h, then loaded on a silica gel cartridge (10 g), eluting with EtOAc (25-50%) in hexane to give the title compound as a white solid (72 mg, 88%). m.p. 174-175° C., HPLC: 99% at 3.01 min (retention time, Phenom. Luna C18, 4.6×50 mm elating with 10-90% MeOH/H2O over 4 minutes containing 0.1% TFA; 4 ml/min, monitoring at 220 inn). MS (ES): m/z=418 [M+1]+. Chiral HPLC 100% e.e.; retention time=34.8 min; Conditions: OD (4.6×250 mm); Eluted with 40% isopropanol in hexane at 1 mL/min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884113B2
Source datasetuspto-grants-2011_02
ORD IDord-570c502e212f4238ab057c313b02fe93
Source noteuspto-grants-2011_02