HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822877Generated: November 1, 2026
Triethylamine → N-(5-isopropyl-1,3-thiazol-2-yl)-butanamide
https://huagongshe.com/reaction/1822877
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | 5-(Propan-2-yl)-1,3-thiazol-2-amine | HCID 10486954 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(5-isopropyl-1,3-thiazol-2-yl)-butanamide | HCID 22170554 | 50.1% |
Reaction Steps
Triethylamine (0.97 ml; 6.34 mmol) and butanoyl chloride (0.52 ml; 5.07 mmol) were added in this order to a solution of 2-amino-5-isopropyl-1,3-thiazole (0.6 g; 4.23 mmol) in dichloromethane (8 ml), cooled to −5° C. The reaction mixture was stirred at −5° C. for 2 hours and then warmed to room temperature. After additional 4 hours, the organic layer was washed with water, saturated sodium bicarbonate, 1N hydrochloric acid, brine, dried over sodium sulfate and evaporated. The residue was recrystallized from cyclohexane to yield 0.45 g (50%) of the title compound as a colourless solid (m.p. 95–97° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07037929B1 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-147b18c32f1741f389eb071fac135d61 |
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| Source note | uspto-grants-2006_05 |
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