Hydrochloric Acid → (R)-3-amino-4-(3'-chloro-biphenyl-4-yl)-2-hydroxy-butyric acid methyl ester hydrochloride
反応式
[CH3:1][O:2][C:3](=[O:29])[C@H:4]([OH:28])[CH:5]([NH:20]C(OC(C)(C)C)=O)[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[CH:14]=2)=[CH:9][CH:8]=1.Cl>O1CCOCC1>[ClH:19].[CH3:1][O:2][C:3](=[O:29])[C@H:4]([OH:28])[CH:5]([NH2:20])[CH2:6][C:7]1[CH:8]=[CH:9][C:10]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([Cl:19])[CH:14]=2)=[CH:11][CH:12]=1参加物
4
実験手順
(R)-3-tert-butoxycarbonylamino-4-(3′-chloro-biphenyl-4-yl)-2-hydroxy-butyric acid methyl ester (113 mg, 0.269 mmol) is treated with 4M HCl in dioxane (2 mL). After being stirred at room temperature for 1 h, the reaction mixture is concentrated. The residue is used for a next step without further purification. HPLC retention time=1.22, 1.29 minutes (condition A): MS (m+1)=320.
後処理
- concentrationthe reaction mixture is concentrated
- customThe residue is used for a next step without further purification
- customHPLC retention time=1.22, 1.29 minutes
出典と根拠
- ORDレコード
- ord-9c8c26279df84bdcb181ad4bca6170be
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08993631B2
反応ノート
読み込み中…