HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Phenethylamine, m-trifluoromethyl- → [4-(1-Methylcyclopropyl)-benzyl]-[2-(3-trifluoromethylphenyl)-ethyl]-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Phenethylamine, m-trifluoromethyl- | HCID 104223 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | (4-Cyclopropylbenzyl)-[2-(4-fluoro-3-trifluoromethylphenyl)-ethyl]-amine | HCID 69342889 | — |
| Edukt | 4-(1-Methylcyclopropyl)benzaldehyde | HCID 86093847 | — |
| Produkt | [4-(1-Methylcyclopropyl)-benzyl]-[2-(3-trifluoromethylphenyl)-ethyl]-amine | HCID 69342738 | 62% |
Reaktionsschritte
The title compound was synthesized in analogy to (4-cyclopropylbenzyl)-[2-(4-fluoro-3-trifluoromethylphenyl)-ethyl]-amine (described in example S53) using 4-(1-methyl-cyclo-propyl)-benzaldehyde (150 mg, 0.94 mmol), 2-(3-trifluoromethylphenyl)-ethylamine (177 mg, 0.94 mmol) and sodium borohydride (53 mg, 1.40 mmol). The isolated residue was purified by flash column chromatography (2%-5% MeOH in EtOAc) to give the desired product (195 mg, 62%) as a colorless oil. MS (ISP) 334.3 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07259183B2 |
| Quelldatensatz | uspto-grants-2007_08 |
| ORD ID | ord-68755597b46146b0a46321230ff37374 |
| Quellennotiz | uspto-grants-2007_08 |