Acetic Acid → HCID 89545047, 화합물

HRID 2283439노트

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HRID 2283439 반응식
[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]

참가 물질

8

실험 절차

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

후처리

  1. stirringAfter stirring for 10 minutes
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe organic liquors were washed with water and brine
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated
  6. customThe residue was purified by silica chromatography
  7. washeluting with 20-100% ethyl acetate/petroleum ether

출처 및 근거

ORD 기록
ord-a0064b92e7794a21989a6ec430afecfc
출처 데이터셋
uspto-grants-2015_09
특허 번호
US09145354B2

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