반응식
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1Cl.O.[NH2:10][NH2:11]>O1CCOCC1.C(O)(C)C>[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][C:7]=1[NH:10][NH2:11]참가 물질
5
반응 조건
- 온도
- 100 °C
실험 절차
A mixture of 3-bromo-4-chloropyridine (5 g, 0.026 mol) and hydrazine hydrate (80% in water, 80 mL) in dioxane (100 mL) was stirred at 100° C. overnight. After cooling down to RT, the mixture was concentrated. The residue was partitioned between 300 mL of EA and 300 mL of aq. sat. NH4Cl. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated to get crude product which was suspended in 30 mL of cold isopropyl alcohol and filtered. The collected solid was dried in air to get 4.2 g (87%) of 3-bromo-4-hydrazinylpyridine as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 8.18 (s, 1H), 8.07 (d, J=5.6 Hz, 1H), 7.37 (s, 1H), 7.01 (d, J=5.6 Hz, 1H), 4.36 (s, 2H).
후처리
- temperatureAfter cooling down to RT
- concentrationthe mixture was concentrated
- customThe residue was partitioned between 300 mL of EA and 300 mL of aq. sat. NH4Cl
- washThe organic layer was washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customto get crude product which
- filtrationfiltered
- customThe collected solid was dried in air
출처 및 근거
- ORD 기록
- ord-b4eb32e1f20a40b28166e7ceb70a9d5a
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09447106B2
연결된 노트
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