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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29574Generated: October 29, 2026

4-(1,3-Oxazol-5-yl)benzenesulphonyl chloride → N-[4-Chloro-2-(6-methyl-pyridine-2-carbonyl)-phenyl]-4-oxazol-5-yl-benzenesulfonamide

https://huagongshe.com/reaction/29574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1,3-Oxazol-5-yl)benzenesulphonyl chlorideHCID 2776415—
Reactant(2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-2-yl)-methanoneHCID 22327312—
ProductN-[4-Chloro-2-(6-methyl-pyridine-2-carbonyl)-phenyl]-4-oxazol-5-yl-benzenesulfonamideHCID 10004078—

Reaction Steps

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 123 mg of (2-Amino-5-chloro-phenyl)-(6-methyl-pyridin-2-yl)-methanone and 122 mg of 4-oxazol-5-yl-benzenesulfonyl chloride 1H-NMR (400 MHz, CDCl3): δ 2.67 (s, 3H), 7.46-7.50 (m, 4H), 7.61-7.70 (m, 4H), 7.65 (m, 2H), 7.94-8.00 (m, 1H), 8.15 (s, 1H). MS: m/z454.0 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420055B2
Source datasetuspto-grants-2008_09
ORD IDord-4412ad56f6a24468aa0fb04043c30732
Source noteuspto-grants-2008_09