HCID 22253953、化合物 → HCID 86593960、化合物
反応式
[C:1]([NH:6][C@H:7]([C:29]([OH:31])=O)[CH2:8][S:9][C:10]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)(=[O:5])[CH:2]([CH3:4])[CH3:3].Cl.[C:33]([S:38][CH2:39][CH2:40][NH2:41])(=[O:37])[CH:34]([CH3:36])[CH3:35]>>[C:1]([NH:6][C@H:7]([C:29]([NH:41][CH2:40][CH2:39][S:38][C:33](=[O:37])[CH:34]([CH3:36])[CH3:35])=[O:31])[CH2:8][S:9][C:10]([C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1)([C:17]1[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=1)[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1)(=[O:5])[CH:2]([CH3:4])[CH3:3]参加物
3
実験手順
The coupling reaction of 13 (3.93 mmol) with S-isobutyrylcysteamine hydrochloride is carried out according to method B described in the first synthetic route (example 1). After the various treatments, the expected compound is isolated by flash chromatography on a silica gel column (eluent: AcOEt/petroleum ether 65%). 15 is collected in the form of a colorless foam with a yield of 75%. Rf (AcOEt/petroleum ether, 5/5): 0.6. [α]D20=+7.9° (c 1.27, CHCl3).
出典と根拠
- ORDレコード
- ord-f885f31b8cb64c25a9c3a7bf6f6a1810
- 出典データセット
- uspto-grants-2005_12
- 特許番号
- US06979747B2
反応ノート
読み込み中…