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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984593Generated: November 1, 2026

Benzenesulfonyl chloride, 2,4-dichloro- → 6-(2,4-Dichloro-benzenesulfonylamino)-3-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-pyridine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/1984593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chloride, 2,4-dichloro-HCID 204419—
ReactantMethyl 6-amino-3-bromopyridine-2-carboxylateHCID 10657127—
Reactant4-(N-piperidinylsulfonyl)thiophenolHCID 57718290—
Product6-(2,4-Dichloro-benzenesulfonylamino)-3-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-pyridine-2-carboxylic acid methyl esterHCID 57718217—

Reaction Steps

Prepared from 2-amino-5-bromo-6-methoxycarbonylpyridine and 4-(N-piperidinylsulfonyl)thiophenol according to General Method 11 step 1 followed by reaction with 2,4-dichlorophenylsulfonyl chloride according to General Method 11 step 2. 1H NMR (CDCl3): 8.02 (1H, d, J 11 Hz, A-ring CH ortho to SO2NH), 7.63 & 7.42 (2×2H, 2×d, 2×J 10 Hz, Ar CH's of C-ring), 7.43 (1H, s, A-ring CH ortho to 2×Cl) 7.32 (1H, d, J 11 Hz, Ar CH), 3.88 (3H, s, CH3) 2.98-2.76 (4H, m, CH2NCH2),), 1.62-1.53 (4H, m, CH2CH2CH2CH2CH2), 1.41-1.30 (2H, m, CH2CH2CH2CH2CH2) further 2 aromatic protons were obscured by a solvent peak around 7.28 ppm. Hplc (Luna 2, Gradient 5): rt=6.55 minutes. LC/MS rt=7.23 minutes, 616/618 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544702B2
Source datasetuspto-grants-2009_06
ORD IDord-78cfa0cebd55438fa8cb83eea54ed561
Source noteuspto-grants-2009_06