HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062677Generated: October 26, 2026
Thiourea → 2-Amino-4-(3-cyanophenyl)-5-carboethoxythiazole
https://huagongshe.com/reaction/1062677
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate | HCID 22282470 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-4-(3-cyanophenyl)-5-carboethoxythiazole | HCID 22282485 | 84% |
Reaction Steps
To a solution of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (2.0 g, 6.75 mmol) in 100 mL of absolute ethanol was added thiourea (0.51 g, 6.75 mmol). The resulting mixture was stirred at 80° C. for 3 h. The reaction was allowed to cool and the solvent was evaporated in vacuo. The residue was taken up in ethyl acetate, washed with saturated aq NaHCO3 and brine, dried (MgSO4) and concentrated in vacuo to yield a solid. Trituration with hexanes/ethyl ether left the title compound as an off-white solid (1.55 g, 65%). 1H NMR (DMSO-d6) δ: 8.03 (s, 1H); 7.93 (s, 2H) ; 7.91 (d, 1H); 7.82 (d, 1H); 7.58 (t, 1H); 4.05 (q, 2H); 1.10 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06962935B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-b93404e3693540fba539d7881408544d |
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| Source note | uspto-grants-2005_11 |
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