Trifluoroacetic acid methylene chloride → cis(+/-)-{(5Z)-5-[2-(4-{[(4-Chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-methoxypiperidin-1-yl)-2-oxoethylidene]-2,4-dioxo-1,3-thiazolidin-3-yl}acetic acid

HRID 43758ノート

反応式

HRID 43758 の反応式
[Cl:1][C:2]1[N:3]=[C:4]([C:9]([NH:11][C@H:12]2[CH2:17][CH2:16][N:15]([C:18](=[O:35])/[CH:19]=[C:20]3/[C:21](=[O:34])[N:22]([CH2:26][C:27]([O:29]C(C)(C)C)=[O:28])[C:23](=[O:25])[S:24]/3)[CH2:14][C@H:13]2[O:36][CH3:37])=[O:10])[NH:5][C:6]=1[CH2:7][CH3:8].FC(F)(F)C(O)=O.ClCCl>CO>[Cl:1][C:2]1[N:3]=[C:4]([C:9]([NH:11][C@H:12]2[CH2:17][CH2:16][N:15]([C:18](=[O:35])/[CH:19]=[C:20]3/[C:21](=[O:34])[N:22]([CH2:26][C:27]([OH:29])=[O:28])[C:23](=[O:25])[S:24]/3)[CH2:14][C@H:13]2[O:36][CH3:37])=[O:10])[NH:5][C:6]=1[CH2:7][CH3:8]

参加物

4

実験手順

tert-Butyl cis(±)-{(5Z)-5-[2-(4-{[(4-chloro-5-ethyl-1H-imidazol-2-yl)carbonyl]amino}-3-methoxypiperidin-1-yl)-2-oxoethylidene]-2,4-dioxo-1,3-thiazolidin-3-yl}acetate obtained in Example (163a) (20.4 mg, 0.04 mmol) was dissolved in methanol (4 mL). A 20% trifluoroacetic acid-dichloromethane solution (5 ml) was added, and the mixture was stirred at room temperature. The organic solvent was evaporated under reduced pressure, and then the residue was washed with ether. The solid was collected by filtration to obtain 7.79 mg of the title compound as a white solid (43%).

後処理

  1. customThe organic solvent was evaporated under reduced pressure
  2. washthe residue was washed with ether
  3. filtrationThe solid was collected by filtration

出典と根拠

ORDレコード
ord-8a46873355bd4fe596100f9b93b7f1d5
出典データセット
uspto-grants-2013_09
特許番号
US08536197B2

反応ノート

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