참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | N-[4-(2-amino-5-nitro-pyridin-3-ylethynyl)-phenyl]-acetamide | HCID 68462435 | — |
| 생성물 | N-(3-(5-Nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)phenyl)acetamide | HCID 68462732 | 68% |
반응 단계
Potassium tert-butoxide (2.25 g, 20 mmol) was added to a solution of N-[4-(2-amino-5-nitro-pyridin-3-ylethynyl)-phenyl]-acetamide (1.48 g, 5 mmol) in a 2:1 mixture of tetrahydrofuran and dimethylformamide (75 mL). The mixture was heated at 70° C. for 16 hours then the tetrahydrofuran was removed in vacuo. The mixture was poured onto a pad of silica and eluted with 10% methanol in ethyl acetate. The organics were concentrated in vacuo to 5% of their original volume and water (30 mL) was added. The resultant orange solid was filtered and dried to afford N-[3-(5-Nitro-1H-pyrrolo[2,3-b]pyridin-2-yl)-phenyl]-acetamide (1.01 g, 68%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07618964B2 |
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| 출처 데이터셋 | uspto-grants-2009_11 |
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| ORD ID | ord-0a838b86e4f04e1d88506577eea423fd |
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| 출처 메모 | uspto-grants-2009_11 |
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