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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644441Generated: October 27, 2026

Hydrochloric Acid → 2-Acetoxy-5-bromo-N-{4-[(1,1-dimethyl)ethyl)-5-piperidinothiazol-2-yl}benzamide

https://huagongshe.com/reaction/644441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant5-Bromo-2-acetylsalicylic acidHCID 73922—
Reactant2-Amino-4-[(1,1-dimethyl)ethyl]-5-piperidinothiazoleHCID 85823492—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
Product2-Acetoxy-5-bromo-N-{4-[(1,1-dimethyl)ethyl)-5-piperidinothiazol-2-yl}benzamideHCID 8660268151.6%

Reaction Steps

Under argon atmosphere, phosphorus oxychloride (46 μl, 0.50 mmol) was added to a mixture of 2-acetoxy-5-bromobenzoic acid (90.3 mg, 0.35 mmol), 2-amino-4-[(1,1-dimethyl)ethyl]-5-piperidinothiazole (80.7 mg, 0.34 mmol), pyridine (0.1 mL) and tetrahydrofuran (3 mL), and the mixture was stirred at room temperature for 2 hours. The reaction mixture was poured into 2N hydrochloric acid and extracted with ethyl acetate. After the organic layer was washed with water and brine, dried over anhydrous sodium sulfate, the residue obtained by evaporation under reduced pressure was purified by chromatography on silica gel (n-hexane:ethyl acetate=3:1) to give the title compound (84.3 mg) as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700655B2
Source datasetuspto-grants-2010_04
ORD IDord-b96fdc81fcec48e99a12c3cef1141f15
Source noteuspto-grants-2010_04