HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1062669Erstellt: 27. Oktober 2026
N-(Phenylmethyl)thiourea → 2-(Benzylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole
https://huagongshe.com/reaction/1062669
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-(Phenylmethyl)thiourea | HCID 737375 | — |
| Edukt | Ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate | HCID 22282470 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 2-(Benzylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole | HCID 22282455 | 49% |
Reaktionsschritte
To a solution of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (0.60 g, 2.03 mmol) in 20 mL of absolute ethanol was added N-benzylthiourea (0.34 g, 2.03 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 (0.36 g, 49%). MS (ESI) 364.1 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06962935B2 |
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| Quelldatensatz | uspto-grants-2005_11 |
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| ORD ID | ord-29e6df5669b54eaba1676aa57785b3be |
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| Quellennotiz | uspto-grants-2005_11 |
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