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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867992Generated: October 26, 2026

Butyric Acid → 4-Fluorobenzenesulfonic acid 2-butyrylaminobenzothiazol-6-yl ester

https://huagongshe.com/reaction/1867992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyric AcidHCID 264—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant4-Fluorobenzenesulfonic acid 2-aminobenzothiazol-6-yl esterHCID 57980814—
SolventDimethylformamideHCID 6228—
Product4-Fluorobenzenesulfonic acid 2-butyrylaminobenzothiazol-6-yl esterHCID 57980796129.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 4-fluorobenzenesulfonic acid 2-aminobenzothiazol-6-yl ester (intermediate 16) (359 mg, 1.107 mmol), butyric acid (146 mg, 1.66 mmol), HATU (631 mg, 1.66 mmol) and N,N-diisopropylethylamine (0.286 ml, 1.66 mmol) in 5.5 ml of dimethylformamide in a 20 ml round-bottomed flask, equipped with a magnetic bar, is stirred for 8 hours at 60° C. and then left overnight at room temperature. The reaction medium is extracted with ethyl acetate and washed with water and then with 0.1 N hydrochloric acid solution. The organic phase is dried over magnesium sulfate, filtered and then evaporated to dryness. The residue obtained (567 mg of pale yellow solid) is purified by chromatography on a 40 g Biotage silica cartridge, eluting with a 9/1 toluene/isopropanol mixture. After evaporating off the solvent, 239 mg of 4-fluorobenzenesulfonic acid 2-butyrylaminobenzothiazol-6-yl ester are obtained (white solid) in a yield of 55%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632952B2
Source datasetuspto-grants-2009_12
ORD IDord-9702059288db4991bb0b4cd14f60b63c
Source noteuspto-grants-2009_12