Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 401493생성일: 2026년 10월 26일
Potassium Carbonate → Tert-butyl 4-(6-(2-amino-5-bromonicotinoyl)pyridin-2-yl)-1,4-diazepane-1-carboxylate
https://huagongshe.com/reaction/401493
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Tert-butyl 1,4-diazepane-1-carboxylate | HCID 2756058 | — |
| 반응물 | (2-Amino-5-bromopyridin-3-yl)(6-fluoropyridin-2-yl)methanone | HCID 57690795 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Tert-butyl 4-(6-(2-amino-5-bromonicotinoyl)pyridin-2-yl)-1,4-diazepane-1-carboxylate | HCID 57690601 | 59% |
반응 단계
A mixture of (2-amino-5-bromopyridin-3-yl)(6-fluoropyridin-2-yl)methanone (190 mg, 0.64 mmol), 1-Boc-homopiperazine (0.14 ml, 0.70 mmol) and potassium carbonate (310 mg, 2.24 mmol) in dimethylformamide (4 ml) was heated at 95° C. for 48 hours. The reaction mixture was cooled down to room temperature and concentrated in vacuo. The residue was slurried in EtOAc and K2CO3 was filtered off. The mother liquors were concentrated in vacuo. The resulting residue was purified on silica gel by flash column chromatography (ISCO Companion|, 12 g column, 0-20% EtOAc/Petrol) to give the title compound as a yellow solid (180 mg, 59% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08741931B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-776fe7358e5843018ec47bbae2422edb |
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| 출처 메모 | uspto-grants-2014_06 |
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