5-Azaindole → HCID 54447290、化合物
反応式
[NH:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[CH:2]1.Br[CH2:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13]>>[C:15]([O:14][C:12](=[O:13])[CH2:11][N:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[CH:2]1)([CH3:18])([CH3:17])[CH3:16]参加物
3
実験手順
The title compound is prepared from 1H-pyrrolo[3,2-c]pyridine as described in EXAMPLES 18 and 19, Part A using tert-butyl bromoacetate in place of methyl iodide. The crude product is purified by column chromatography eluting with a gradient of 3% MeOH/CH2Cl2 to 6% MeOH/CH2Cl2 to give the title compound as an oil.
後処理
- customThe crude product is purified by column chromatography
- washeluting with a gradient of 3% MeOH/CH2Cl2 to 6% MeOH/CH2Cl2
出典と根拠
- ORDレコード
- ord-b83882fafd474bdaa10245e91d475de6
- 出典データセット
- uspto-grants-2001_08
- 特許番号
- US06281227B1
反応ノート
読み込み中…