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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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Tert-butyl 1,4-diazepane-1-carboxylateHCID 2756058—
반응물(2-Amino-5-bromopyridin-3-yl)(6-fluoropyridin-2-yl)methanoneHCID 57690795—
용매DimethylformamideHCID 6228—
생성물Tert-butyl 4-(6-(2-amino-5-bromonicotinoyl)pyridin-2-yl)-1,4-diazepane-1-carboxylateHCID 5769060159%

반응 조건

온도95 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741931B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-776fe7358e5843018ec47bbae2422edb
출처 메모uspto-grants-2014_06