4-Cyanophenylboronic acid → 1-[2-(4-Cyanophenyl)cyclopenten-1-yl]-4-(methylthio)benzene
反応式
Br[C:2]1[CH2:6][CH2:5][CH2:4][C:3]=1[C:7]1[CH:12]=[CH:11][C:10]([S:13][CH3:14])=[CH:9][CH:8]=1.[C:15]([C:17]1[CH:22]=[CH:21][C:20](B(O)O)=[CH:19][CH:18]=1)#[N:16]>>[C:15]([C:17]1[CH:22]=[CH:21][C:20]([C:2]2[CH2:6][CH2:5][CH2:4][C:3]=2[C:7]2[CH:12]=[CH:11][C:10]([S:13][CH3:14])=[CH:9][CH:8]=2)=[CH:19][CH:18]=1)#[N:16]参加物
3
実験手順
Following the synthetic procedure outlined in Step 3 of Example 1, 500 mg (1.9 mmol) of 1-bromocyclopenten-1-yl)-4-methylthio) benzene (Example 1, Step 2) was reacted with 540 mg 3.7 mmol) of 4-cyanophenylboronic acid (Step 1 Purification by silica gel chromatography (MPLC) with hexane ethyl acetate (19:1) gave 480 mg (89%) of 1-[2-(4-cyanophenyl)cyclopenten-1-yl]-4-(methylthio)benzene as an oil: NMR (CDCl3) d 2.07 (m, J=7 Hz, 2H), 2.42 (s, 3H), 2.89 (t, J=7 Hz, 4H), 7.05 (d, J=8 Hz, 2H), 7.11 (d, J=8 Hz, 2H), 7.26 (d, J=8 Hz, 2H), 7.48 (d, J=8 Hz, 2H).
後処理
- customStep 1 Purification by silica gel chromatography (MPLC) with hexane ethyl acetate (19:1)