Tributyltin Chloride → N,N-dimethyl-3-(6-methyl-3-(tributylstannyl)-1H-indazol-1-yl)propan-1-amine
반응식
I[C:2]1[C:10]2[C:5](=[CH:6][C:7]([CH3:11])=[CH:8][CH:9]=2)[N:4]([CH2:12][CH2:13][CH2:14][N:15]([CH3:17])[CH3:16])[N:3]=1.C([Mg]Cl)(C)C.[CH2:23]([Sn:27]([CH2:33][CH2:34][CH2:35][CH3:36])([CH2:29][CH2:30][CH2:31][CH3:32])Cl)[CH2:24][CH2:25][CH3:26]>C1COCC1>[CH3:16][N:15]([CH3:17])[CH2:14][CH2:13][CH2:12][N:4]1[C:5]2[C:10](=[CH:9][CH:8]=[C:7]([CH3:11])[CH:6]=2)[C:2]([Sn:27]([CH2:29][CH2:30][CH2:31][CH3:32])([CH2:33][CH2:34][CH2:35][CH3:36])[CH2:23][CH2:24][CH2:25][CH3:26])=[N:3]1참가 물질
반응 조건
- 온도
- -20 °C
실험 절차
A solution of 3-(3-iodo-6-methyl-1H-indazol1-yl)-N,N-dimethylpropan-1-amine (400 mg, 1.2 mmol) in 20 mL of dry THF was cooled to −20° C. under nitrogen atmosphere, then isopropylmagnesium chloride (1.2 mL, 2.4 mmol, 2M in THF) was added and stirred for 15 min at −20° C. Then tributylchlorostannane (0.7 mL, 2.4 mmol) was added and allowed to warm to room temperature. The reaction was cooled in an ice bath and quenched with saturated ammonium chloride solution, product extracted with ethyl acetate (3×50 mL), combined organics dried with sodium sulfate and concentrated to give N,N-dimethyl-3-(6-methyl-3-(tributylstannyl)-1H-indazol-1-yl)propan-1-amine (1.2 g, crude) as an oil which was used in the next step directly without further purification.
후처리
- temperatureto warm to room temperature
- temperatureThe reaction was cooled in an ice bath
- customquenched with saturated ammonium chloride solution, product
- extractionextracted with ethyl acetate (3×50 mL)
- dry with materialcombined organics dried with sodium sulfate
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-8b6c18f1c09b490093d1001231401444
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08658646B2
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