関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine | HCID 18541030 | — |
| 反応物 | 3-(4-Cyanoanilino)propyl 4-methylbenzenesulfonate | HCID 21867652 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-({3-[3-Azabicyclo[3.2.1]oct-8-yl(methyl)amino]propyl}amino)benzonitrile | HCID 18540907 | 65.5% |
反応手順
A mixture of 3-benzyl-N-methyl-3-azabicyclo[3.2.1]octan-8-amine (Preparation B; 4.0 g, 17.4 mmol), 3-(4-cyanoanilino)propyl 4-methyl-benzenesulfonate (Preparation G(ii); 5.74 g, 17.4 mmol), and potassium carbonate (2.40 g, 17.4 mmol) in DMF (85 mL) was heated at 90° C. under nitrogen overnight. The mixture was partitioned with water (200 mL) and diethyl ether (150 mL). The aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic extracts were washed with brine (2×30 mL), dried (Na2SO4), filtered and then concentrated in vacuo. The residue was chromatographed on silica gel, eluting with dichloromethane:methanol (98:2), to afford 3.40 g (50%) of the sub-title compound as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06559162B2 |
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| 出典データセット | uspto-grants-2003_05 |
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| ORD ID | ord-159d2fdcc8c34753ace01f967dbd9955 |
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| 出典メモ | uspto-grants-2003_05 |
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