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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968197Generated: October 25, 2026

Diisopropylethylamine → 2-Amino-5-[(3-carbomethoxyphenyl)thio]thiazole

https://huagongshe.com/reaction/968197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-AcetylpiperazineHCID 83795—
ReactantHOAtHCID 181649—
Reactant2-Tert-butoxycarbonylamino-5-[(3-carboxyphenyl)thio]thiazoleHCID 22170420—
SolventTetrahydrofuranHCID 8028—
Product2-Amino-5-[(3-carbomethoxyphenyl)thio]thiazoleHCID 22288371100.1%

Reaction Conditions

Temperature55 °C

Reaction Steps

A suspension of 2-tert-butoxycarbonylamino-5-[(3-carboxyphenyl)thio]thiazole (528 mg, 1.5 mmol), N-acetylpiperazine (239 mg, 1.87 mmol), ethyl-3-(3-dimethylamino)propyl carbodiimide hydrochloride (400 mg, 2 mmol), 1-hydroxy-7-azabenzotriazole (272 mg, 2 mmol) and diisopropylethylamine (560 μL, 4 mmol) in THF (20 mL) was heated to 55° C. for 2 h. The mixture was cooled to rt. and concentrated. The residue was purified using column chromatography on silica gel eluted with 2% methanol in dichloromethane followed by 5% methanol in dichloromethane to obtain the titled compound (400 mg, 58%) as a white foam. E. 4-Acetyl-1-[3-[(2-aminothiazol-5-yl)thio]benzoyl]piperazine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06958336B2
Source datasetuspto-grants-2005_10
ORD IDord-91836e50768442dd81257eedc01a7dac
Source noteuspto-grants-2005_10