참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | methyl 3-formyl-1H-indole-6-carboxylate | HCID 735867 | — |
| 반응물 | Sodium cyanoborohydride | HCID 5003444 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Sulfolane | HCID 31347 | — |
| 생성물 | Methyl 3-methyl-1H-indole-6-carboxylate | HCID 21938240 | 91.3% |
반응 단계
A mixture of methyl 3-formyl-1H-indole-6-carboxylate (12.0 g), p-toluenesulphonic acid (2.0 g) and p-toluenesulphonylhydrazide (13.0 g) in a mixture of dimethylformamide (100 ml) and sulpholane (50 ml) was heated at 100° C. for 15 minutes and then cooled to room temperature. The mixture was treated with sodium cyanoborohydride (15.0 g, 5 g portions after 10 minute intervals), then heated at 100° C. for 2 hours. After cooling to ambient temperature the reaction mixture was treated with ice water (500 ml) giving a white precipitate. Water (1000 ml) was added and the mixture stirred for 30 minutes then filtered. The off-white solid was washed with warm water then azeotroped with toluene to yield the title compound (10.2 g) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06800645B1 |
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| 출처 데이터셋 | uspto-grants-2004_10 |
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| ORD ID | ord-bfce7c81643c40b4a05d1623efd7841b |
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| 출처 메모 | uspto-grants-2004_10 |
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