4-(2-chloroethoxy)-1H-indole → HCID 21703085、化合物
反応式
[NH:1]1[C:9]2[C:4](=[C:5]([O:10][CH2:11][CH2:12]Cl)[CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[NH:14]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[C:15]1C(C)CCN>>[NH:14]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[C:16]([CH:4]([CH3:5])[CH2:3][CH2:2][NH:1][CH2:12][CH2:11][O:10][C:5]2[CH:6]=[CH:7][CH:8]=[C:9]3[C:4]=2[CH:3]=[CH:2][NH:1]3)=[CH:15]1参加物
3
実験手順
This compound was prepared in the manner described above for Example 5 using 2-(1H-indol-4-yloxy)ethylchloride and 3-indolyl-butylamine in 43% yield as an off-white solid: mp 70-73° C.
後処理
- customThis compound was prepared in the manner
出典と根拠
- ORDレコード
- ord-fa8eacfc4c9a45cd8d65440c3722ea3a
- 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…