HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1,2-Dichloroethane → 4-(2,2-Difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1,2-Dichloroethane | HCID 11 | — |
| Edukt | Citric Acid | HCID 311 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | HOAt | HCID 181649 | — |
| Edukt | 4-Carboxy-3-fluorophenylboronic acid | HCID 2763201 | — |
| Edukt | 2,2-Difluoro-1-phenylethan-1-amine | HCID 45282641 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-(2,2-Difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acid | HCID 123534983 | — |
Reaktionsschritte
To a solution of 4-borono-2-fluorobenzoic acid (200 mg, 1.087 mmol), 2,2-difluoro-1-phenylethanamine (232 mg, 1.196 mmol), and DIEA (0.570 mL, 3.26 mmol) in THF (3.866 mL) and DMF (0.483 mL) was added HOAt (296 mg, 2.175 mmol) and EDC (521 mg, 2.72 mmol). After 3 h stirring at room temperature, 10% citric acid solution was added (pH ˜3) and extracted with 2-methyl THF and EtOAc (1:1). The organic layers were dried over anhydrous Na2SO4, filtered, and concentrated. The crude 4-(2,2-difluoro-1-phenylethylcarbamoyl)-3-fluorophenylboronic acid was obtained (90%) and used for the next step without purification. LCMS (m/z): 375.3 (MH+), 0.48 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09242996B2 |
| Quelldatensatz | uspto-grants-2016_01 |
| ORD ID | ord-10da6daac0da476486f9959ec4a2ca54 |
| Quellennotiz | uspto-grants-2016_01 |