関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 4-Methylpiperazine-1-ethylamine | HCID 70284 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 2-Amino-5-bromonicotinaldehyde hydrobromide | HCID 86606146 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 5-Bromo-3-((2-(4-methylpiperazin-1-yl)ethylamino)methyl)pyridin-2-amine | HCID 67154522 | — |
反応手順
Triethylamine (1.0 mL, 7.09 mmol) was added to a solution of 2-amino-5-bromonicotinaldehyde hydrobromide (1.0 g, 3.54 mmol) in methanol (24 mL) at room temperature. The reaction mixture was stirred for 10 minutes prior to the addition of 2-(4-methylpiperazin-1-yl)ethanamine (558 mg, 3.90 mmol). The reaction mixture was then stirred overnight and cooled to 0° C. Sodium borohydride (201 mg, 5.32 mmol) was added portionwise at 0° C. and the reaction mixture was allowed to reach room temperature and stirred for 4 hours. After concentration to dryness, the residue was purified by chromatography on silica gel using dichloromethane/methanol/ammoniac (10:0:0.1 to 9:1:0.1) as eluent. The title product was obtained as a yellow solid (560 mg, 48%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846711B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-39900b3f3ff04ae5b23668af34e3bc84 |
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| 出典メモ | uspto-grants-2014_09 |
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