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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889715Generated: October 27, 2026

Triethylamine → 3,5-Dichloro-N-((4',6-dichlorobiphenyl-3-yl)methyl)-N-(4-fluorobenzyl)-2-hydroxybenzenesulfonamide

https://huagongshe.com/reaction/1889715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-Dichloro-2-hydroxybenzenesulphonyl chlorideHCID 90078—
Reactant1-(4',6-Dichlorobiphenyl-3-yl)-N-(4-fluorobenzyl)methanamineHCID 58531663—
SolventDichloromethaneHCID 6344—
Product3,5-Dichloro-N-((4',6-dichlorobiphenyl-3-yl)methyl)-N-(4-fluorobenzyl)-2-hydroxybenzenesulfonamideHCID 5853139346%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(4′,6-Dichlorobiphenyl-3-yl)-N-(4-fluorobenzyl)methanamine (200 mg, 0.555 mmol, 1.0 eq) was dissolved in dry DCM and the resulting solution was stirred for 10 minutes and cooled to 0° C. Triethylamine (168 mg, 1.6 mmol, 3 eq) was added to the above solution and the mixture was stirred for 10 minutes. 3,5-Dichloro-2-hydroxybenzene-1-sulfonyl chloride dissolved in DCM was added slowly over a period of 10 minutes and the mixture was stirred for 4 h at ambient temperature. The solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography on silica gel (60-120) eluting with 5-10% ethyl acetate/hexane to give the title compound (0.14 g, 46%). 1H NMR (400 MHz, CD3OD) δ 4.47 (s, 2H), 4.53 (s, 2H), 6.91-6.98 (m, 3H), 7.12-7.15 (m, 1H), 7.22-7.27 (m, 4H), 7.33-7.35 (d, 1H), 7.43-7.45 (d, 2H), 7.54 (d, 1H), 7.67 (d, 1H). MS (ESI): 583.8 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-a92bfb03bfd44eb4bd45cd826d133a83
Source noteuspto-grants-2013_08