Hydrochloric Acid → (RS)-3-[4-[1-(4-tert-Butylphenyl)-3-(4-trifluoromethoxyphenyl)ureidomethyl]benzoylamino}-2-hydroxypropionic Acid
反応式
C([O:3][C:4](=[O:43])[CH:5]([OH:42])[CH2:6][NH:7][C:8](=[O:41])[C:9]1[CH:14]=[CH:13][C:12]([CH:15]([NH:26][C:27]([NH:29][C:30]2[CH:35]=[CH:34][C:33]([O:36][C:37]([F:40])([F:39])[F:38])=[CH:32][CH:31]=2)=[O:28])[C:16]2[CH:21]=[CH:20][C:19]([C:22]([CH3:25])([CH3:24])[CH3:23])=[CH:18][CH:17]=2)=[CH:11][CH:10]=1)C.[OH-].[Na+].Cl>C(O)C>[C:22]([C:19]1[CH:18]=[CH:17][C:16]([CH:15]([NH:26][C:27]([NH:29][C:30]2[CH:35]=[CH:34][C:33]([O:36][C:37]([F:38])([F:39])[F:40])=[CH:32][CH:31]=2)=[O:28])[C:12]2[CH:13]=[CH:14][C:9]([C:8]([NH:7][CH2:6][CH:5]([OH:42])[C:4]([OH:43])=[O:3])=[O:41])=[CH:10][CH:11]=2)=[CH:21][CH:20]=1)([CH3:25])([CH3:23])[CH3:24]参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
A solution of 3-{4-[1-(4-tert-butylphenyl)-3-(4-trifluoromethoxyphenyl)ureidomethyl]benzoylamino}-2-hydroxypropionic acid ethyl ester was stirred in absolute ethanol (20 mL) and 1 M sodium hydroxide (6 mL) was added. Stirring was continued for 17 hours and the solution was acidified with aqueous hydrochloric acid. The solvent was decanted and the remaining oil was dissolved in acetonitrile (20 mL) by heating. Water (20 mL) was added dropwise under vigorous stirring and the mixture was allowed to cool to room temperature. The precipitate was filtered off, washed with water and dried to afford 0.51 g (43%) of the title compound as a solid.
後処理
- customThe solvent was decanted
- dissolutionthe remaining oil was dissolved in acetonitrile (20 mL)
- temperatureby heating
- additionWater (20 mL) was added dropwise
- stirringunder vigorous stirring
- filtrationThe precipitate was filtered off
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-d5b4cbd0943243a7b44db2374e93aab5
- 出典データセット
- uspto-grants-2005_10
- 特許番号
- US06953812B2
反応ノート
読み込み中…