Acetic Acid → HCID 89545047、化合物
反応式
[C:1]([C:9]1[C:10]([F:18])=[C:11]([CH:14]=[CH:15][C:16]=1[Cl:17])[CH:12]=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[CH2:20]([O:22][C:23](=[O:28])[CH2:24][C@@H:25]([NH2:27])[CH3:26])[CH3:21].C(N(CC)CC)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(O)(=O)C.C(=O)(O)[O-].[Na+]>ClC(Cl)C>[CH2:20]([O:22][C:23](=[O:28])[CH2:24][C@@H:25]([NH:27][CH2:12][C:11]1[CH:14]=[CH:15][C:16]([Cl:17])=[C:9]([C:1](=[O:8])[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:10]=1[F:18])[CH3:26])[CH3:21]参加物
反応物 6
生成物 1
試薬・触媒・溶媒 1
実験手順
Step 1 To a solution of 3-benzoyl-4-chloro-2-fluoro-benzaldehyde (Intermediate 10, 337 mg, 1.29 mmol) in dichloroethane (5 ml) was sequentially added (S)-3-amino-butyric acid ethyl ester hydrochloride (237 mg, 1.41 mmol), triethylamine (0.196 ml, 1.41 mmol), sodium triacetoxyborohydride (818 mg, 3.86 mmol) and glacial acetic acid (0.159 ml 2.57 mmol). The mixture was stirred for 2 days then dilute sodium bicarbonate was added. After stirring for 10 minutes, the mixture was extracted with ethyl acetate. The organic liquors were washed with water and brine, dried (MgSO4) and concentrated. The residue was purified by silica chromatography eluting with 20-100% ethyl acetate/petroleum ether furnishing (3S)-3-(3-benzoyl-4-chloro-2-fluoro-benzylamino)-butyric acid ethyl ester as a colourless oil (203 mg). MS: [M+H] 378
後処理
- stirringAfter stirring for 10 minutes
- extractionthe mixture was extracted with ethyl acetate
- washThe organic liquors were washed with water and brine
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customThe residue was purified by silica chromatography
- washeluting with 20-100% ethyl acetate/petroleum ether
出典と根拠
- ORDレコード
- ord-a0064b92e7794a21989a6ec430afecfc
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09145354B2
反応ノート
読み込み中…