1-(2-Chloroethyl)-2,6-dimethylpiperidine → alpha-(o-Fluorophenyl)-alpha-[2-(diisopropylamino)ethyl]-alpha-[2-(2,6-dimethyl-1-piperidinyl)ethyl]acetonitrile
反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]([CH2:11][CH2:12][N:13]([CH:17]([CH3:19])[CH3:18])[CH:14]([CH3:16])[CH3:15])[C:9]#[N:10].Cl[CH2:21][CH2:22][N:23]1[CH:28]([CH3:29])[CH2:27][CH2:26][CH2:25][CH:24]1[CH3:30]>>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]([CH2:11][CH2:12][N:13]([CH:17]([CH3:19])[CH3:18])[CH:14]([CH3:15])[CH3:16])([CH2:21][CH2:22][N:23]1[CH:28]([CH3:29])[CH2:27][CH2:26][CH2:25][CH:24]1[CH3:30])[C:9]#[N:10]参加物
3
実験手順
Substitution of equivalent quantities of α-(o-fluorophenyl)-α-[2-(diisopropylamino)ethyl]acetonitrile and 1-(2-chloroethyl)-2,6-dimethylpiperidine in the procedure of Example 2, Method B, and substantial repetition of the procedure detailed therein, affords α-(o-fluorophenyl)-α-[2-(diisopropylamino)ethyl]-α-[2-(2,6-dimethyl-1-piperidinyl)ethyl]acetonitrile, as an oil boiling at about 170°-175° C. at 0.3 mm. pressure.
出典と根拠
- ORDレコード