HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Trichloroacetonitrile → 3-chloro-4-[(3,4-dimethoxyphenyl)methoxy]-N-methyl-N-[2-[[(1-methylethyl)amino]carbonyl]-4-phenoxyphenyl]-benzamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Trichloroacetonitrile | HCID 11011 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | N-isopropyl-2-(methylamino)-5-phenoxybenzamide | HCID 57796896 | — |
| Edukt | 4-(3,4-Dimethoxybenzyloxy)-3-chlorobenzoic acid | HCID 57796897 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-chloro-4-[(3,4-dimethoxyphenyl)methoxy]-N-methyl-N-[2-[[(1-methylethyl)amino]carbonyl]-4-phenoxyphenyl]-benzamide | HCID 57796888 | 87,7% |
Reaktionsschritte
A slurry of 1B (28 mg, 0.09 mmol) and trichloroacetonitrile (0.009 mL, 0.09 mmol) in CH2Cl2 (1 mL) at room temperature was treated with a solution of triphenylphosphine (22 mg, 0.09 mmol) in THF (0.25 mL). The reaction mixture was stirred for 30 minutes and additional trichloroacetonitrile (0.009 mL, 0.09 mmol) and triphenylphosphine (22 mg, 0.09 mmol) were added. The resulting solution was treated with 44B (16 mg, 0.06 mmol) in CH2Cl2 (0.5 mL). The stirring was continued for 2 hours, and then the reaction concentrated to dryness. The residue was purified by chromatography (SiO2, 50% to 75% EtOAc in hexanes) to afford 44C (31 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07569725B2 |
| Quelldatensatz | uspto-grants-2009_08 |
| ORD ID | ord-2c90fc973cc74432bb313e260acb7af5 |
| Quellennotiz | uspto-grants-2009_08 |