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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417284Generated: November 2, 2026

Hydrochloric Acid → N-(4-biphenyl-3-yl-thiazol-2-yl)-4-methyl-benzenesulfonamide

https://huagongshe.com/reaction/1417284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantN-(4-biphenyl-3-yl-thiazol-2-yl)-N-methoxymethyl-4-methyl-benzenesulfonamideHCID 21845572—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-biphenyl-3-yl-thiazol-2-yl)-4-methyl-benzenesulfonamideHCID 2184558545.9%

Reaction Steps

A solution of 0.29 g of N-(4-biphenyl-3-yl-thiazol-2-yl)-N-methoxymethyl-4-methyl-benzenesulfonamide in 6 ml of tetra-hydrofuran was stirred at room temperature for 6 hours after the addition of 1.5 ml of 6N hydrochloric acid. The reaction mixture was added to 40 ml of water and extracted with ethyl acetate. The organic phases were combined, dried with magnesium sulphate and concentrated. Recrystallization from 10 ml of 50% ethanol yielded 120 mg of N-(4-biphenyl-3-yl-thiazol-2-yl)-4-methyl-benzenesulfonamide as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877193
Source datasetuspto-grants-1999_03
ORD IDord-485f8b76b32441aead511284301b7f8c
Source noteuspto-grants-1999_03