HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1385188Generated: October 31, 2026
Triethylamine → [[2-(acetylamino)-5-thiazolyl]thio]-N-(2-oxobutyl)acetamide
https://huagongshe.com/reaction/1385188
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | [[2-(Acetylamino)-5-thiazolyl]thio]acetic acid | HCID 5329677 | — |
| Reactant | 1-aminobutan-2-one Hydrochloride | HCID 11607912 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [[2-(acetylamino)-5-thiazolyl]thio]-N-(2-oxobutyl)acetamide | HCID 10946551 | 90% |
Reaction Steps
A mixture of [[2-(acetylamino)-5-thiazolyl]thio]acetic acid (9.0 g, 38.8 mmol), HOBT (5.94 g, 38.8 mmol) and ethyldimethylaminopropylcarbodiimide hydrochloride salt (11.16 g, 58.2 mmol) in DMF (50 mL) was stirred at 0° C. for 0.5 h. To this mixture was added 1-amino-2-butanone hydrochloride (5.27 g, 42.7 mmol) followed by triethylamine (15 mL, 107.5 mmol). The mixture was stirred at 0° C. for 0.5 h and at rt for 1 h. Water (200 mL) was added to the mixture and the product was extracted with methylene chloride containing 10% MeOH (5×100 mL). The methylene chloride extract was dried over Na2SO4 and concentrated. The residue was triturated with water and the precipitated solid product was collected by filtration. It was dried to obtain the desired product (10.5 g, 90%), mp 195-196° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06262096B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-6aa4e51b9eb349bbab4f57ade73f04a4 |
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| Source note | uspto-grants-2001_07 |
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