関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Methylamine | HCID 6329 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 1-methyl-1H-indole-5-carbaldehyde | HCID 7537534 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | n-Methyl-1-(1-methyl-1h-indol-5-yl)methanamine | HCID 18525753 | 100% |
反応手順
N-Methylindole-5-carbaldehyde (800 mg, 5.1 mmol) was dissolved in anhydrous methanol (15 mL). Methylamine (7.15 mL of 2M solution in methanol, 15.3 mmol) was added and the reaction was stirred for 3 hr. The solution was concentrated to a yellow oil and then dissolved into anhydrous methanol (15 mL). Sodium borohydride (194 mg, 5.1 mmol) was added and the mixture was stirred overnight. Water (1 mL) was added and the solution was concentrated to an orange oil. Sodium hydroxide (5 mL, 1N) was added and the product was extracted with ethyl acetate (3×20 mL), dried over MgSO4 and concentrated to afford the title compound as an orange oil (885 mg, 100%). 1H NMR (200 MHz, CDCl3) δ 7.57 (s, 1H), 7.35-7.11 (m, 3H), 6.51 (d, J=2.9 Hz, 1H), 3.85 (s, 2H), 3.79 (s, 3H), 2.48 (s, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07879872B2 |
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| 出典データセット | uspto-grants-2011_02 |
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| ORD ID | ord-6822850dad1b4f67aceff249dd8bc064 |
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| 出典メモ | uspto-grants-2011_02 |
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