참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Methyl-2-butene | HCID 10553 | — |
| 반응물 | Monobasic potassium phosphate | HCID 516951 | — |
| 반응물 | 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehyde | HCID 2838253 | — |
| 반응물 | Sodium Chlorite | HCID 23668197 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 용매 | tert-Butanol | HCID 6386 | — |
| 생성물 | 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxylic acid | HCID 58944728 | 101.1% |
반응 단계
To a suspension of 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxaldehyde (Compound 50, 150 mg, 0.51 mmol) in acetonitrile (6 ml), tert-butanol (6 ml) and H2O (6 ml) was added 2-methyl-2-butene (4 ml), potassium phosphate monobasic (1.4 g, 10.2 mmol), sodium chlorite (80%, 1.15 g, 10.2 mmol). The mixture was stirred at room temperature for 20 h, more potassium phosphate monobasic (0.35 g, 2.6 mmol) and sodium chlorite (80%, 0.29 g, 2.6 mmol) were added and stirred at room temperature for 24 h. The solvent was removed under reduced pressure. The residue solid was washed with H2O (×3) and filtered, dissolved in acetone and filtered to yield 1-benzyl-2-methyl-5-nitro-1H-indole-3-carboxylic acid (Compound 51) as a yellow powder (160 mg, 100%). 1H-NMR (ACETONE-d6) δ 2.83 (s, 3 H), 5.68 (s, 2 H), 7.06-7.15 (m, 2 H), 7.25-7.41 (m, 3 H), 7.68 (d, J=9.1 Hz, 1 H), 8.10 (dd, J =9.1, 2.3 Hz, 1 H), 9.11 (d, J=2.3 Hz, 1 H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737173B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-7a744141b8f04f279f740449c088f55b |
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| 출처 메모 | uspto-grants-2010_06 |
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