4-(Quinolin-2-ylmethoxy)benzyl alcohol → 2-(4-Chloromethylphenoxy)methylquinoline
反応式
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][C:13]1[CH:20]=[CH:19][C:16]([CH2:17]O)=[CH:15][CH:14]=1.[Cl:21]C1C=C2C(C=CC(COC3C=CC(CO)=CC=3)=N2)=CC=1>>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][C:13]1[CH:20]=[CH:19][C:16]([CH2:17][Cl:21])=[CH:15][CH:14]=1参加物
3
実験手順
The procedure from Example 6, part B was used except 4-(quinolin-2-ylmethoxy)benzyl alcohol was substituted for 4-(7-chloroquinolin-2-ylmethoxy)benzyl alcohol. The intermediate was obtained in 47% yield.
後処理
- customThe intermediate was obtained in 47% yield
出典と根拠
- ORDレコード
- ord-43a1e498f73c49d4ad930a4bcb5a4155
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05622969
反応ノート
読み込み中…