Indole-3-Butyric Acid → 3-Indolyl-butyramide
反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[CH2:10][CH2:11][C:12]([NH2:14])=[O:13].N1C2C(=CC=CC=2)C(CCCC(O)=O)=[CH:16]1.C(N1C=CN=C1)(N1C=CN=C1)=O>>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[CH:10]([CH3:16])[CH2:11][C:12]([NH2:14])=[O:13]参加物
4
実験手順
This compound was prepared in the manner described above for (18a), using 3-indolebutyric acid and 1,1'-carbonyldimidazole. A 96% yield was obtained as a off-white solid: mp 86-87° C.
後処理
- customThis compound was prepared in the manner
- customA 96% yield was obtained as a off-white solid
出典と根拠
- ORDレコード
- ord-249859463c734e24ac4a0f36d77fc5ed
- 出典データセット
- uspto-grants-2000_09
- 特許番号
- US06121307
反応ノート
読み込み中…