5-Chloro-1H-indole-2-carboxylic acid → HCID 178523869、化合物
反応式
Cl.[NH2:2][C@@H:3]([CH2:13][C:14]1[N:15]=[CH:16][NH:17][CH:18]=1)[C:4]([N:6]1[CH2:11][CH2:10][CH:9]([OH:12])[CH2:8][CH2:7]1)=[O:5].[Cl:19][C:20]1[CH:21]=[C:22]2[C:26](=[CH:27][CH:28]=1)[NH:25][C:24]([C:29](O)=[O:30])=[CH:23]2>>[OH:12][CH:9]1[CH2:8][CH2:7][N:6]([C:4](=[O:5])[C@@H:3]([NH:2][C:29]([C:24]2[NH:25][C:26]3[C:22]([CH:23]=2)=[CH:21][C:20]([Cl:19])=[CH:28][CH:27]=3)=[O:30])[CH2:13][C:14]2[N:15]=[CH:16][NH:17][CH:18]=2)[CH2:11][CH2:10]1参加物
3
実験手順
(S)-2-Amino-1-(4-hydroxy-piperidin-1-yl)-3-(1H-imidazol-4-yl)-propan-1-one hydrochloride (0.7 mmol) and 5-chloro-1H-indole-2-carboxylic acid (0.7 mmol) were coupled according to Procedure A (120 hour reaction time, acid wash omitted). The crude product was triturated twice with ether, with 1:1 ether-hexanes and the residue purified by chromatography on silica gel eluted with 5-20% ethanol in dichloromethane containing 0.5% ammonium hydroxide. Yield 232 mg, 81%; HPLC (40/60) 2.57 minutes (98%); PBMS 416/418 (MH+, 100%);
後処理
- customThe crude product was triturated twice with ether, with 1:1 ether-hexanes
- customthe residue purified by chromatography on silica gel
- washeluted with 5-20% ethanol in dichloromethane containing 0.5% ammonium hydroxide
- customHPLC (40/60) 2.57 minutes (98%)
出典と根拠
- ORDレコード
- ord-bf6c6a6f40e142de9c8c6f6ccffa719f
- 出典データセット
- uspto-grants-2001_08
- 特許番号
- US06277877B1
反応ノート
読み込み中…