Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | Ethyl 2,4-dimethylthiazole-5-carboxylate | HCID 603810 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18712270 | HCID 18712270 | 50.3% |
Reaction Steps
3.0 g of ethyl 2,4-dimethylthiazole-5-carboxylate, 7.0 g of ethylamine hydrochloride, 6.0 g of triethylamine, and 100 mL of ethanol were added into a 250 mL of high-pressure reactor. And the reaction mixture was heated to 120-160° C. and stirred for 20 to 30 hours, and then extracted with ethyl acetate, the organic layer was separated while the aqueous layer was extracted with ethyl acetate twice. The organic phases were combined, and dried over anhydrous sodium sulfate after washed with an iced aqueous sodium chloride solution twice, then remove the solvent under reduced pressure to obtain 1.5 g N-ethyl-2,4-dimethylthiazole-5-carboxamide which was used in the next step directly without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09386769B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-ad7988916cd4472db2bcdd322c9dc517 |
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| Source note | uspto-grants-2016_07 |
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