Hydrochloric Acid → Isobutyric acid (1s,2s)-6-fluoro-2-[2-({3-[(2-fluoro-ethyl)-(3-methoxy-2-methoxymethyl-2-methyl-propyl)-amino]-propyl}-methyl-amino)-ethyl]-1-isopropyl-1,2,3,4-tetrahydro-naphthalen-2-yl ester dihydrochloride salt
反応式
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C@H:8]([CH:12]([CH3:14])[CH3:13])[C@@:7]([O:35][C:36](=[O:40])[CH:37]([CH3:39])[CH3:38])([CH2:15][CH2:16][N:17]([CH2:19][CH2:20][CH2:21][N:22]([CH2:32][CH2:33][F:34])[CH2:23][C:24]([CH2:29][O:30][CH3:31])([CH3:28])[CH2:25][O:26][CH3:27])[CH3:18])[CH2:6][CH2:5]2.[ClH:41]>CCOC(C)=O>[ClH:41].[ClH:41].[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C@H:8]([CH:12]([CH3:14])[CH3:13])[C@@:7]([O:35][C:36](=[O:40])[CH:37]([CH3:39])[CH3:38])([CH2:15][CH2:16][N:17]([CH2:19][CH2:20][CH2:21][N:22]([CH2:32][CH2:33][F:34])[CH2:23][C:24]([CH2:29][O:30][CH3:31])([CH3:28])[CH2:25][O:26][CH3:27])[CH3:18])[CH2:6][CH2:5]2参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
411 mg of isobutyric acid (1S,2S)-6-fluoro-2-[2-({3-[(2-fluoro-ethyl)-(3-methoxy-2-methoxymethyl-2-methyl-propyl)-amino]-propyl}-methyl-amino)-ethyl]-1-isopropyl-1,2,3,4-tetrahydro-naphthalen-2-yl ester were dissolved in 10 mL EtOAc, the solution was cooled with an ice bath and 2.4 mL of 3M HCl in EtOAC were added. The reaction mixture was evaporated to dryness without heating to give the desired isobutyric acid (1S,2S)-6-fluoro-2-[2-({3-[(2-fluoro-ethyl)-(3-methoxy-2-methoxymethyl-2-methyl-propyl)-amino]-propyl}-methyl-amino)-ethyl]-1-isopropyl-1,2,3,4-tetrahydro-naphthalen-2-yl ester dihydrochloride salt.
後処理
- temperaturethe solution was cooled with an ice bath
- customThe reaction mixture was evaporated to dryness
- temperaturewithout heating
出典と根拠
- ORDレコード
- ord-8d691f5156da42f4949101d52fe5495e
- 出典データセット
- uspto-grants-2013_05
- 特許番号
- US08436205B2
反応ノート
読み込み中…