HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062670Generated: October 26, 2026
Methylthiourea → 2-(Methylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole
https://huagongshe.com/reaction/1062670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylthiourea | HCID 2723704 | — |
| Reactant | Ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate | HCID 22282470 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Methylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole | HCID 22282463 | 73% |
Reaction Steps
To a solution of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (0.65 g, 2.2 mmol) in 20 mL of tetrahydrofuran was added N-methylthiourea (0.20 g, 2.2 mmol). The resulting mixture was stirred at 65° C. for 16 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 (0.46 g, 73%). MS (ESI) 288.3 (M+H)+.
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-8d02aa7c04fe4e08bf4cbdbd2d5fb687 |
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| Source note | uspto-grants-2005_11 |
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