참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethylamine hydrochloride | HCID 11198 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 반응물 | Ethyl 3-methyl-4-oxopiperidine-1-carboxylate | HCID 15075657 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 1-Carbethoxy-4-ethylamino-3-methylpiperidine | HCID 22278900 | — |
반응 단계
Ethylamine hydrochloride (5 g, 61.34 mmol) was added to the stirred solution of 1-carbethoxy-3-methyl-4-piperidone (3.5 g, 18.9 mmol) obtained as described in Preparation 1, in methanol (30 ml) followed by 3.43 g (61.34 mmol) KOH. Stirring was continued for 3 hr at ambient temperature. The resulting mixture was cooled at 0° C. and sodium cyanoborohydride (1.4 g, 22.22 mmol) was added to it. Cooling was removed after 10 min. and resulting mixture was stirred for 16 hr at ambient temperature. The reaction mixture was concentrated to dryness, triturated with water, acidified with conc. HCl (pH 3˜4) and extracted with ethyl acetate to remove impurities. The aqueous layer was basified with 1 M sodium hydroxide solution (pH˜10) and extracted with ethyl acetate. Ethyl acetate extract was dried (Na2SO4) and, concentrated to dryness to give 1-carbethoxy-4-ethylamino-3-methylpiperidine. Yield 2.3 g (54%), C11H22N2O2, m/z 215 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06878713B2 |
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| 출처 데이터셋 | uspto-grants-2005_04 |
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| ORD ID | ord-a38b431759e645758c14daa8fa0f3cf1 |
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| 출처 메모 | uspto-grants-2005_04 |
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