2-(Bromomethyl)pyridine → Carbamic acid 1-{3-[4-(pyridin-2-ylmethoxy)-phenyl]-isoxazol-5-yl}-ethyl ester
反応式
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:19]=[C:18]([CH:20]([O:22][C:23](=[O:25])[NH2:24])[CH3:21])[O:17][N:16]=2)=[CH:11][CH:10]=1)[C:2]1C=[CH:6][CH:5]=[CH:4][CH:3]=1.BrCC1C=CC=C[N:29]=1>>[N:29]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:1][O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:19]=[C:18]([CH:20]([O:22][C:23](=[O:25])[NH2:24])[CH3:21])[O:17][N:16]=2)=[CH:11][CH:10]=1参加物
3
実験手順
The compound was synthesized using carbamic acid 1-[3-(4-benzyloxy-phenyl)-isoxazol-5-yl]-ethyl ester of example 117 in the same manner as in Example 10 by debenzylation following reaction with 2-bromomethylpyridine.
後処理
- customThe compound was synthesized
出典と根拠
- ORDレコード
- ord-3cae1a8ecd6e471b98a7d5133f42f89e
- 出典データセット