Toluene → HCID 19738050、化合物
反応式
Cl[CH2:2][CH2:3][CH2:4][N:5]1[CH2:10][CH:9]([CH3:11])[O:8][CH:7]([CH3:12])[CH2:6]1.[H-].[Na+].[Cl:15][C:16]1[CH:24]=[CH:23][C:19]([CH2:20][C:21]#[N:22])=[CH:18][CH:17]=1.C1(C)C=CC=CC=1>CN(C=O)C>[Cl:15][C:16]1[CH:24]=[CH:23][C:19]([CH:20]([CH2:2][CH2:3][CH2:4][N:5]2[CH2:10][CH:9]([CH3:11])[O:8][CH:7]([CH3:12])[CH2:6]2)[C:21]#[N:22])=[CH:18][CH:17]=1参加物
6
実験手順
This intermediate (2.0 g.) was prepared using the procedure described in Example 2a except using 2.3 g. (11 moles) of 4-(3-chloropropyl)-2,6-dimethylmorpholine, 0.48 g. of sodium hydride, and 1.69 g. (11 mmoles) of 4-chlorobenzyl cyanide in 15 ml. of a 2 to 1 mixture of toluene and DMF and was isolated as a pale yellow oil.
後処理
- customThis intermediate (2.0 g.) was prepared
- customwas isolated as a pale yellow oil
出典と根拠
- ORDレコード
- ord-78d7f8d414b24a0c95ca254035ff6810
- 出典データセット
- uspto-grants-1993_08
- 特許番号
- US05240925
反応ノート
読み込み中…