6-Methoxyisoquinoline-3-carboxylic acid → 3-Isoquinolinecarboxylic acid, 7-methoxy-
反応式
CO[C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[N:8][C:7]([C:13]([OH:15])=[O:14])=[CH:6]2.[C:16](C1(C(O)=O)C2C(=CC=C(O)C=2)CCN1)(OC(C)(C)C)=[O:17]>>[CH3:16][O:17][C:12]1[CH:11]=[C:10]2[C:5]([CH:6]=[C:7]([C:13]([OH:15])=[O:14])[N:8]=[CH:9]2)=[CH:4][CH:3]=1参加物
3
実験手順
0.25 g (17% in 4 steps) 7-methoxy-isoquinoline-3-carboxylic acid was prepared according to procedure described for the synthesis of 6-methoxy-isoquinoline-3-carboxylic acid (in Example 294) starting from 2.0 g (6.8 mmol) of boc-7-hydroxy-tetrahydroisoquinoline carboxylic acid using 179 mg (0.824 mmol). LCMS: 204 (M+1)+.
出典と根拠
- ORDレコード
- ord-20822131d2f14539801c82758d84a190
- 出典データセット
- uspto-grants-2011_02
- 特許番号
- US07893267B2
反応ノート
読み込み中…