참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | 1-Heptanamine | HCID 8127 | — |
| 반응물 | 1-Methylindole-2-carboxaldehyde | HCID 267164 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | N-heptyl-N-[(1-methylindol-2-yl)methyl]amine | HCID 68855834 | 61% |
반응 단계
To a solution of 1-methylindole-2-carbaldehyde (1.59 g, 10.0 mmol) and heptylamine (1.49 mL, 10.0 mmol) in ethanol (50 mL) were added acetic acid (2.3 mL, 40 mmol) and sodium cyanoborohydride (0.75 g, 12.0 mmol) and the reaction mixture was stirred at room temperature overnight. Water (5 mL) was added and the mixture was concentrated in vacuo. The residue was taken up in ethyl acetate (75 mL) and aqueous 1 M KOH (75 mL) and the phases were separated. The aqueous layer was extracted with ethyl acetate (2×75 mL) and the combined organic phase was washed with brine (75 mL), dried over Na2SO4, and concentrated in vacuo. Purification on a column of silica gel (130 g) with ethyl acetate (17-33% gradient) in heptane as the eluent yielded 1.57 g (61%) of a yellow oil, which solidified upon standing.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07488844B2 |
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| 출처 데이터셋 | uspto-grants-2009_02 |
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| ORD ID | ord-184d1136bece4a75ba16d8502b7d67e2 |
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| 출처 메모 | uspto-grants-2009_02 |
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