Triethylsilane → 4-benzyl-6-[(5-bromo-2-chloro-phenyl)methyl]spiro[3H-1,4-benzoxazine-2,1'-cyclopropane]
반응식
[CH2:1]([N:8]1[C:15]2[CH:16]=[C:17]([CH:20]([C:22]3[CH:27]=[C:26]([Br:28])[CH:25]=[CH:24][C:23]=3[Cl:29])O)[CH:18]=[CH:19][C:14]=2[O:13][C:10]2([CH2:12][CH2:11]2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([SiH](CC)CC)C.OS(C(F)(F)F)(=O)=O>FC(F)(F)C(O)=O>[CH2:1]([N:8]1[C:15]2[CH:16]=[C:17]([CH2:20][C:22]3[CH:27]=[C:26]([Br:28])[CH:25]=[CH:24][C:23]=3[Cl:29])[CH:18]=[CH:19][C:14]=2[O:13][C:10]2([CH2:12][CH2:11]2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 50 °C
실험 절차
To an ice cold solution of (4-benzylspiro[3H-1,4-benzoxazine-2,1′-cyclopropane]-6-yl)-(5-bromo-2-chloro-phenyl)methanol (780 mg, 1.7 mmol) in trifluoroacetic acid (4 mL) was added triethylsilane (1.32 mL, 8.3 mmol) followed by triflic acid (0.15 mL, 1.7 mmol). After heating the mixture for 15 min at 50° C., the reaction was cooled to room temperature. Trifluoroacetic acid was evaporated under reduced pressure, and the resulting residue was taken in saturated aq. sodium bicarbonate solution and extracted with ethyl acetate. The organic layer was washed with water, brine, dried over sodium sulfate, and concentrated. The resulting residue was purified by silica gel column chromatography to furnish 4-benzyl-6-[(5-bromo-2-chloro-phenyl)methyl]spiro[3H-1,4-benzoxazine-2,1-cyclopropane] (715 mg).
후처리
- temperaturethe reaction was cooled to room temperature
- customTrifluoroacetic acid was evaporated under reduced pressure
- extractionextracted with ethyl acetate
- washThe organic layer was washed with water, brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated
- customThe resulting residue was purified by silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-ecc8d4ab3956491c9793b0c23cf6af61
- 출처 데이터셋
- uspto-grants-2012_04
- 특허 번호
- US08163704B2
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