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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 2-Tert-butoxycarbonylamino-5-[(3-carboxyphenyl)thio]thiazole | HCID 22170420 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Amino-5-[(3-carbomethoxyphenyl)thio]thiazole | HCID 22288371 | 100.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06958336B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-91836e50768442dd81257eedc01a7dac |
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| Source note | uspto-grants-2005_10 |
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