참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | Ethyl 4-methoxy-1H-pyrrolo[2,3-b]pyridine-2-carboxylate | HCID 11736140 | — |
| 반응물 | 1-benzyl-2-methyl-1H-pyrrole | HCID 12643084 | — |
| 반응물 | 1-benzyl-5-methyl-1H-pyrrole-2-carbaldehyde | HCID 59170380 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (4-methoxy-1H-pyrrolo[2,3-b]pyridin-2-yl)methanol | HCID 15885418 | — |
| 생성물 | 1-benzyl-5-methyl-1H-pyrrole-2-carbaldehyde | HCID 59170380 | — |
반응 단계
1-Benzyl-5-methyl-1H-pyrrole-2-carbaldehyde, 4: POCl3 (23.46 mL, 246 mmol) was added dropwise to a stirred N,N-dimethyformamide (204 mL) at 0° C. After addition the mixture was stirred for additional 90 minutes. To the mixture was added dropwise the solution of 1-benzyl-2-methyl-1H-pyrrole, 3 (2.71 g, 45 mmol) in tetrahydrofuran (1150 mL). The reaction mixture was allowed to be stirred for 18 h from 0° C. to room temperature. The mixture was concentrated and redissolved in ethyl acetate (2 L). The mixture was washed with saturated Na2CO3 (2×500 mL). The Na2CO3 solution was extracted with ethyl acetate (7×1 L). The organic layers were combined and concentrated. The crude product was purified by silica gel chromatography (hexane to hexane:ethyl acetate, 7:1) to afford 1-benzyl-5-methyl-1H-pyrrole-2-carbaldehyde, 4 as a light yellow liquid. Yield: 30.8 g (81%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07666898B2 |
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| 출처 데이터셋 | uspto-grants-2010_02 |
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| ORD ID | ord-156d251a788a494ea4ce7d0095a8794d |
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| 출처 메모 | uspto-grants-2010_02 |
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