Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 5-(2-Bromoacetyl)pyrazole-3-carboxylic acid ethyl ester | HCID 178469076 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178468667 | HCID 178468667 | 71.9% |
Reaction Steps
A mixture of 5-(2-bromoacetyl)pyrazole-3-carboxylic acid ethyl ester (6.2 g), thiourea (1.8 g), and ethanol (100 ml) was stirred at 60° C. for 30 minutes and concentrated. The residue was dissolved in 100 ml of 1N HCl solution, and washed with ethyl ether (2×100 ml). The aqueous solution was neutralized with NaHCO3. The resulting precipitates were collected through a filtration to afford 4.05 g of 5-(2-aminothiazol-4-yl)pyrazole-3-carboxylic acid ethyl ester as brown solids, mp 205°-207° C. NMR: 1.40 (t, 3H), 4.39 (q, 2H), 5.8 (bs, 2H), 6.85 (s, 1H), 7.03 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05470862 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-2011c5952d114905b28b6c34b1407d30 |
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| Source note | uspto-grants-1995_11 |
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