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Methanol → N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-4-(4-fluorophenoxy)benzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methanol | HCID 887 | — |
| 反応物 | Diphenyl chlorophosphate | HCID 75654 | — |
| 反応物 | (3R)-1-Azabicyclo(2.2.2)octan-3-amine | HCID 719215 | — |
| 反応物 | 4-(4-Fluorophenoxy)benzoic acid | HCID 5005163 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-[(3R)-1-azabicyclo[2.2.2]oct-3-yl]-4-(4-fluorophenoxy)benzamide | HCID 9924044 | 85.2% |
反応手順
TEA (50 μL, 0.35 mmol) is added to a suspension of the acid from Step F (81 mg, 0.35 mmol) in CH2Cl2 (1 mL). Diphenylchlorophosphate (62 μL, 0.3 mmol) is added and the resulting solution is stirred at room temperature for 30 minutes. A solution of (R)-3-aminoquinuclidine (1.0M in CH3CN, 0.2 mL, 0.2 mmol) is added and the resulting solution is shaken overnight at room temperature. MeOH is added and the mixture is poured through a column of AG50W×2 ion exchange resin (H+ form). The resin is washed with MeOH and then the product is eluted with 5% TEA in MeOH. The eluent is evaporated to dryness to yield the desired product (58 mg, 85%). MS for C20H21FN2O2 (ESI) (M+H)+ m/z 341.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06479510B2 |
| 出典データセット | uspto-grants-2002_11 |
| ORD ID | ord-7083cc2633834f7ba5f83c5c9cf1f6a5 |
| 出典メモ | uspto-grants-2002_11 |