Potassium Carbonate → (S)-3-(2-Amino-7-isopropyl-4-methyl-benzothiazol-6-ylsulfanyl)-4-hydroxy-6-[2-(4-hydroxyl-phenyl)-ethyl]-6-isopropyl-5,6-dihydro-pyran-2-one
反応式
[NH2:1][C:2]1[S:3][C:4]2[C:10]([CH:11]([CH3:13])[CH3:12])=[C:9]([S:14]S(C3C=CC(C)=CC=3)(=O)=O)[CH:8]=[C:7]([CH3:25])[C:5]=2[N:6]=1.[OH:26][C:27]1[CH2:32][C@@:31]([CH2:36][CH2:37][C:38]2[CH:43]=[CH:42][C:41]([OH:44])=[CH:40][CH:39]=2)([CH:33]([CH3:35])[CH3:34])[O:30][C:29](=[O:45])[CH:28]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[NH2:1][C:2]1[S:3][C:4]2[C:10]([CH:11]([CH3:12])[CH3:13])=[C:9]([S:14][C:28]3[C:29](=[O:45])[O:30][C@:31]([CH2:36][CH2:37][C:38]4[CH:43]=[CH:42][C:41]([OH:44])=[CH:40][CH:39]=4)([CH:33]([CH3:35])[CH3:34])[CH2:32][C:27]=3[OH:26])[CH:8]=[C:7]([CH3:25])[C:5]=2[N:6]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
The title compound was prepared according to General Method 16a using toluene-4-thiosulfonic acid S-(2-amino-7-isopropyl-4-methyl-benzothiazol-6-yl)ester (Example BB-5; 0.35 g, 1.27 mmol), (S)-4-hydroxy-6-[2-(4-hydroxy-phenyl)-ethyl]-6-isopropyl-5,6-dihydro-pyran-2-one (Example J-10; 0.35 g. 1.27 mmol), potassium carbonate (0.7 g), and DMF (5 mL). The crude reaction mixture was purified by flash chromatography (20% EtOAc in hexanes to 50% EtOAc in hexanes to 5% MeOH in EtOAc as eluents), mp 232-234° C. MS (APCI): 513 (M+H).
後処理
- customThe crude reaction mixture
- customwas purified by flash chromatography (20% EtOAc in hexanes to 50% EtOAc in hexanes to 5% MeOH in EtOAc as eluents), mp 232-234° C
出典と根拠
- ORDレコード
- ord-59d822f8a46140da8edcf4e033b9238c
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06852711B2
反応ノート
読み込み中…