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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867991Generated: November 2, 2026

Propionic Acid → 4-Fluorobenzenesulfonic acid 2-propionylaminobenzothiazol-6-yl ester

https://huagongshe.com/reaction/1867991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionic AcidHCID 1032—
ReactantDiisopropylamineHCID 7912—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant4-Fluorobenzenesulfonic acid 2-aminobenzothiazol-6-yl esterHCID 57980814—
SolventDimethyl SulfoxideHCID 679—
SolventDimethylformamideHCID 6228—
Product4-Fluorobenzenesulfonic acid 2-propionylaminobenzothiazol-6-yl esterHCID 5798082469.2%

Reaction Steps

A solution of 4-fluorobenzenesulfonic acid 2-aminobenzothiazol-6-yl ester (intermediate 16) (500 mg, 1.14 mmol), propionic acid (253 mg, 3.42 mmol), HBTU (1.23 g, 3.42 mmol) and N,N-diisopropylamine (737 mg, 5.7 mmol) in 6.5 ml of dimethylformamide is stirred overnight at room temperature. The reaction medium is evaporated to dryness. The dry residue is extracted twice with 50 ml of ethyl acetate and washed with water. The organic phase is then washed with saturated sodium chloride solution. The organic phase is dried over magnesium sulfate and then evaporated. The oil obtained is dissolved in 35 ml of dimethyl sulfoxide and then purified 7 times by preparative HPLC on a Nucléodur C18, 100′10 μm reverse-phase column with a gradient over 52 minutes of 5% to 95% acetonitrile supplemented with 0.07% trifluoroacetic acid in water, supplemented with 0.07% trifluoroacetic acid. The flow rate is 70 ml/min. The fractions containing the clean product are concentrated to give 300 mg of 4-fluorobenzenesulfonic acid 2-propionylaminobenzothiazol-6-yl ester in a yield of 69%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632952B2
Source datasetuspto-grants-2009_12
ORD IDord-ad8249cdd216415aa205fd3ade20c991
Source noteuspto-grants-2009_12