反応式
CC1C=CN=CC=1.N1C=CC([C:14]2[CH:18]=[CH:17][O:16][C:15]=2[C:19]([O:21][CH2:22][CH3:23])=[O:20])=CC=1>>[O:16]1[CH:17]=[CH:18][CH:14]=[C:15]1[C:19]([O:21][CH2:22][CH3:23])=[O:20]参加物
3
実験手順
In a manner similar to that in Reference Example 13, by using 4-methylpyridine in place of 3,4-dimethylpyridine and using ethyl 3-(4-pyridyl)furan-2-carboxylate (133 mg, 0.612 mmol) obtained in Step 1, in place of ethyl furan-2-carboxylate, the entitled Compound ad (35.3 mg, 18%) was obtained.
出典と根拠
- ORDレコード
- ord-0a9cf6d669a9439d8ae342e165398303
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08889718B2
関連ノート
読み込み中…