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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252712Generated: November 1, 2026

2,4-Dimethoxybenzenesulfonyl chloride → HCID 11655984, compound

https://huagongshe.com/reaction/252712

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dimethoxybenzenesulfonyl chlorideHCID 2734626—
ReactantN-[5-(5-amino-6-chloropyridin-3-yl)-4-methyl-1,3-thiazol-2-yl]acetamideHCID 86244450—
SolventPyridineHCID 1049—
ProductHCID 11655984HCID 1165598427.3%

Reaction Steps

2,4-Dimethoxyphenylsulfonyl chloride (J. Med. Chem., 1977, 20, 1235; 376 mg) was added to a stirred solution of N-[5-(5-amino-6-chloropyridin-3-yl)-4-methyl-1,3-thiazol-2-yl]acetamide (150 mg) in pyridine (1.5 mL) and the resultant solution was heated at 50° C. for 16 hours. The mixture was cooled to room temperature and concentrated by evaporation. The residue was purified by preparative HPLC on Kromasil C18 reversed-phase silica using a solvent gradient of 10% to 100% acetonitrile in water (containing 1% acetic acid) as eluent at a flow rate of about 10 mL/minute. The material so obtained was triturated under diethyl ether to give the title compound as a white solid (70 mg); 1H NMR Spectrum: (DMSOd6) 2.16 (s, 3H), 2.29 (s, 3H), 3.76 (s, 3H), 3.83 (s, 3H), 6.60 (m, 1H), 6.69 (d, 1H), 9.64 (d, 1H), 6.75 (d, 1H), 8.25 (br s, 1H), 9.80 (s, 1H); Mass Spectrum: M+H+ 483.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868188B2
Source datasetuspto-grants-2011_01
ORD IDord-9877341aff524c58bf8b8332b80fd407
Source noteuspto-grants-2011_01