Tributyltin Chloride → HCID 178448230, 화합물
반응식
[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6](I)=[N:7][NH:8]2)=[C:4]([F:12])[CH:3]=1.[H-].[Na+].C([Mg]Cl)(C)C.[CH2:20]([Sn:24](Cl)([CH2:29][CH2:30][CH2:31][CH3:32])[CH2:25][CH2:26][CH2:27][CH3:28])[CH2:21][CH2:22][CH3:23].[Cl-].[NH4+]>C1COCC1.C(OCC)(=O)C>[Cl:1][C:2]1[CH:10]=[C:9]2[C:5]([C:6]([Sn:24]([CH2:25][CH2:26][CH2:27][CH3:28])([CH2:29][CH2:30][CH2:31][CH3:32])[CH2:20][CH2:21][CH2:22][CH3:23])=[N:7][NH:8]2)=[C:4]([F:12])[CH:3]=1참가 물질
반응 조건
- 온도
- -15 °C
실험 절차
6-Chloro-4-fluoro-3-iodo-1H-indazole (10.1 g, 34.1 mmol) was dissolved in THF (170 ml). The reaction flask was stirred in a water bath and sodium hydride (60% dispersion, 1.64 g, 40.9 mmol) was added. The mixture was stirred for 15 min then cooled in an ice/salt bath to −15° C. Isopropylmagnesium chloride (2.0 M in THF, 20.6 ml, 41.2 mmol) was added dropwise. After 40 min, tributyltin chloride (11.6 ml, 42.6 mmol) was slowly added and the reaction was allowed to warm to room temperature. After an additional 2 h stirring, ammonium chloride solution and ethyl acetate were added. The layers were separated and the aqueous layer was extracted once more with ethyl acetate. The combined organic layers were washed with sodium chloride solution and dried over sodium sulfate. Evaporation of the solvent provided 6-chloro-4-fluoro-3-tributylstannanyl-1H-indazole as an oil which was used directly in the next step.
후처리
- stirringThe mixture was stirred for 15 min
- temperatureto warm to room temperature
- stirringAfter an additional 2 h stirring
- customThe layers were separated
- extractionthe aqueous layer was extracted once more with ethyl acetate
- washThe combined organic layers were washed with sodium chloride solution
- dry with materialdried over sodium sulfate
- customEvaporation of the solvent
출처 및 근거
- ORD 기록
- ord-093b8c6b071e431c99b8100cffdcde51
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08658646B2
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