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[CH:1]([C:3]1[CH:8]=[CH:7][C:6](OS(C2C=CC(C)=CC=2)(=O)=O)=[CH:5][CH:4]=1)=[O:2].[C:20]([C:22]1[CH2:27][CH2:26][CH2:25][CH2:24][CH:23]=1)#[CH:21]>CCCCCCC.C(Cl)Cl>[C:22]1([C:20]#[C:21][C:6]2[CH:5]=[CH:4][C:3]([CH:1]=[O:2])=[CH:8][CH:7]=2)[CH2:27][CH2:26][CH2:25][CH2:24][CH:23]=1참가 물질
4
실험 절차
This product was prepared from toluene-4-sulfonic acid 4-formyl-phenyl ester and 1-ethynyl-cyclohexene following the general procedure for the Sonogashira cross-coupling process described above. Chromatography eluent: heptane/DCM 1:1; yield (71 mg, 68%); 1H NMR δ (CDCl3): 9.99 (s, 1H), 8.02 (d, J=8.51 Hz, 2H), 7.52 (d, J=8.60 Hz, 2H), 6.31-6.27 (m, 1H), 2.14-2.22 (m, 4H), 1.58-1.73 (m, 4H); LCMS m/z: 210.
후처리
- customyield (71 mg, 68%)
출처 및 근거
- ORD 기록
- ord-160872d07e834ee496b7f5f4013d03b5
- 출처 데이터셋
- uspto-grants-2013_07
- 특허 번호
- US08487109B2
연결된 노트
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