Hydrochloric Acid → (E)-2-{4-[2-(-tert-Butoxycarbonylamino-phenylcarbamoyl)-vinyl]-phenyl}-5-chloro-pentanoic acid
反応式
C[O:2][C:3](=[O:34])[CH:4]([C:9]1[CH:14]=[CH:13][C:12](/[CH:15]=[CH:16]/[C:17](=[O:33])[NH:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=2NC(OC(C)(C)C)=O)=[CH:11][CH:10]=1)[CH2:5][CH2:6][CH2:7][Cl:8].[Li+].[OH-:36].Cl>CO.O>[C:4]([O:36][C:17]([NH:18][N:18]([C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[C:17](/[CH:16]=[CH:15]/[C:12]1[CH:13]=[CH:14][C:9]([CH:4]([CH2:5][CH2:6][CH2:7][Cl:8])[C:3]([OH:2])=[O:34])=[CH:10][CH:11]=1)=[O:33])=[O:33])([CH3:9])([CH3:5])[CH3:3]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of (E)-2-{4-[2-(2-tert-butoxycarbonylamino-phenylcarbamoyl)-vinyl]-phenyl}-5-chloro-pentanoic acid methyl ester (48.7 mg, 10 mmol) in MeOH/H2O (4:1) (2 mL), LiOH (24 mg, 100 mmol) was added. After the solution was stirred at room temperature for 5 h, the solution was neutralized with 2N HCl to pH 5-6. The mixture was evaporated to dryness under reduced pressure, then EtOAc (10 mL) was added. The organic layer was washed with brine, dried with Na2SO4, filtered, and evaporated to obtain of a yellow solid product without further purification. MS: calc'd 473 (MH+), exp 473 (MH+). 1H NMR (400 MHz, DMSO-d6) 12.50 (s, 1H), 9.73 (s, 1H), 8.50 (s, 1H), 6.89-7.64 (m, 10H), 3.61 (m, 3H), 1.55-2.10 (m, 4H), 1.46 (s, 9H).
後処理
- customThe mixture was evaporated to dryness under reduced pressure
- additionEtOAc (10 mL) was added
- washThe organic layer was washed with brine
- dry with materialdried with Na2SO4
- filtrationfiltered
- customevaporated
- customto obtain of a yellow solid product without further purification
出典と根拠
- ORDレコード
- ord-06f672c9f4084e9a9fa90d1f6068ff3b
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08202866B2
反応ノート
読み込み中…