反応式
[CH3:1][C:2]1[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=1[C:9]1[O:10][CH2:11][C:12]([CH3:15])([CH3:14])[N:13]=1.[CH3:16][O:17][C:18]1[CH:19]=[C:20]([CH:23]=[CH:24][CH:25]=1)[CH2:21]Cl>>[CH3:16][O:17][C:18]1[CH:19]=[C:20]([CH2:21][CH2:1][C:2]2[CH:7]=[C:6]([CH3:8])[CH:5]=[CH:4][C:3]=2[C:9]2[O:10][CH2:11][C:12]([CH3:15])([CH3:14])[N:13]=2)[CH:23]=[CH:24][CH:25]=1参加物
3
実験手順
The subtitle compound was prepared from the product of example 15 step (iii) (20 g) and 3-methoxybenzyl chloride (17.4 ml) by the method of example 15 step (iv). Purification was by chromatography eluting with 5-10% ethyl acetate in isohexane. Yield 20.53 g. MS: APCI(+ve): 324 (M+1).
後処理
- customPurification
- washeluting with 5-10% ethyl acetate in isohexane
出典と根拠
- ORDレコード
- ord-bc4350c96f7f451a94aa710a435535ca
- 出典データセット
- uspto-grants-2000_08
- 特許番号
- US06107297
関連ノート
読み込み中…