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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889711Generated: November 2, 2026

Triethylamine → HCID 44595537, compound

https://huagongshe.com/reaction/1889711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-Dichloro-2-hydroxybenzenesulphonyl chlorideHCID 90078—
ReactantHCID 58531406HCID 58531406—
SolventDichloromethaneHCID 6344—
ProductHCID 44595537HCID 4459553750%

Reaction Steps

A solution of 1-(4′-chloro-2-methoxybiphenyl-3-yl)-N-(4-fluorobenzyl)methanamine (590 mg, 1.684 mmol, 1.0 eq) in dry DCM under nitrogen at 0° C. and treated slowly with triethylamine (492 mg, 4.8 mmol, 3 eq). The reaction mixture was stirred for 10 minutes and treated with a solution of 3,5-dichloro-2-hydroxybenzene-1-sulfonyl chloride (527 mg, 2.018 mmol, 1.2 eq) dissolved in DCM. The resulting mixture was stirred for 12 h at ambient temperature and concentrated under reduced pressure. The residue was further diluted with water and extracted with ethyl acetate. The organic layer was dried under anhydrous Na2SO4 and concentrated. The residue was purified by flash column chromatography on silica gel (60-120) eluting with 15-20% ethyl acetate/hexane to afford the title compound (0.400 g, 50%). 1H NMR (400 MHz, DMSO-d6) δ 3.32 (s, 3H), 4.52-4.53 (d, 4H), 7.04-7.08 (m, 3H), 7.17-7.24 (m, 4H), 7.43-7.52 (m, 5H), 7.77 (s, 1H). MS (ESI): 577.8 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-26b5f9a47d774808aea186a5b679c809
Source noteuspto-grants-2013_08