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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867965Generated: October 29, 2026

Water → 4-Fluorobenzenesulfonic acid 2-aminobenzothiazol-6-yl ester

https://huagongshe.com/reaction/1867965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoroacetic acidHCID 6422—
Reactant4-Fluorobenzenesulfonic acid 2-tert-butoxycarbonylaminobenzo-thiazol-6-yl esterHCID 57980860—
SolventDichloromethaneHCID 6344—
Product4-Fluorobenzenesulfonic acid 2-aminobenzothiazol-6-yl esterHCID 57980814112.2%

Reaction Steps

A solution of 4-fluorobenzenesulfonic acid 2-tert-butoxycarbonylaminobenzo-thiazol-6-yl ester (intermediate 15) (1.7 g, 3.60 mmol), 10 ml of trifluoroacetic acid (130 mmol) in 10 ml of dichloromethane, and 1 ml of water, in a 100 ml round-bottomed flask equipped with a magnetic bar, is stirred for 2 hours at room temperature. The reaction medium is evaporated to dryness and the residue obtained is washed with ethyl ether to give 1.31 g of 4-fluoro-benzenesulfonic acid 2-aminobenzothiazol-6-yl ester in the form of the trifluoroacetic acid salt (white powder) in a yield of 83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632952B2
Source datasetuspto-grants-2009_12
ORD IDord-338e7cc0cde5422c9577d7773a06d449
Source noteuspto-grants-2009_12