Hydrochloric Acid → n-((5s)-3-(4-(2s-(Pyrimidin-2-yl)thiomethyl-2,5-dihydropyrrol-4-yl)phenyl)-2-oxooxazolidin-5-ylmethyl)acetamide
反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[S:7][CH2:8][CH:9]1[CH:13]=[C:12]([C:14]2[CH:19]=[CH:18][C:17]([N:20]3[CH2:24][C@H:23]([CH2:25][NH:26][C:27](=[O:29])[CH3:28])[O:22][C:21]3=[O:30])=[CH:16][CH:15]=2)[CH2:11][N:10]1C(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.Cl.CC(C)=O.Cl>CC(C)=O.O>[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[S:7][CH2:8][CH:9]1[CH:13]=[C:12]([C:14]2[CH:19]=[CH:18][C:17]([N:20]3[CH2:24][C@H:23]([CH2:25][NH:26][C:27](=[O:29])[CH3:28])[O:22][C:21]3=[O:30])=[CH:16][CH:15]=2)[CH2:11][NH:10]1参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
The N-trityl compound (Example 30, 0.528 g, 0.79 mM) in acetone (8 ml) at 0° C. was treated with freshly prepared HCl/acetone (4 ml) and stirred. The mixture was periodically treated with 10% HCl in water until TLC indicated consumption of starting material. The reaction mixture was then diluted with EtOAc (30 ml) and taken to pH 11 with NH4OH solution. The aqueous layer was extracted with EtOAc and the combined organics dried (MgSO4) and evaporated to a residue which was triturated with diethyl ether to give the title amine (0.309 g, 92%) which was used without further purification.
後処理
- customconsumption of starting material
- additionThe reaction mixture was then diluted with EtOAc (30 ml)
- extractionThe aqueous layer was extracted with EtOAc
- dry with materialthe combined organics dried (MgSO4)
- customevaporated to a residue which
- customwas triturated with diethyl ether
出典と根拠
- ORDレコード
- ord-0030985c8ff84c79b30fcf1ac4e763f2
- 出典データセット
- uspto-grants-2003_08
- 特許番号
- US06605630B1
反応ノート
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