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4-Chlorobenzaldehyde → HCID 67230285, 화합물

HRID 386481
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HRID 386481 반응식
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([F:14])=[C:6]([N:8]2[CH2:12][CH2:11][CH2:10][C:9]2=[O:13])[CH:7]=1.[Cl:15][C:16]1[CH:23]=[CH:22][C:19]([CH:20]=O)=[CH:18][CH:17]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl>[Cl:15][C:16]1[CH:23]=[CH:22][C:19]([CH2:20][NH:1][C:2]2[CH:3]=[CH:4][C:5]([F:14])=[C:6]([N:8]3[CH2:12][CH2:11][CH2:10][C:9]3=[O:13])[CH:7]=2)=[CH:18][CH:17]=1
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참가 물질

5

반응물 3

HCID 77264-ChlorobenzaldehydeHCID 5049666Sodium triacetoxyborohydrideHCID 167718851-(5-Amino-2-fluorophenyl)-2-pyrrolidinone

생성물 1

HCID 67230285HCID 67230285, 화합물수율 44.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 1-(5-amino-2-fluoro-phenyl)-pyrrolidin-2-one (0.34 g, 1.8 mmol), 4-chlorobenzaldehyde (0.25 g, 1.8 mmol) and sodium triacetoxyborohydride (0.75 g 3.6 mmol) was stirred in dry dichloromethane (25 ml) overnight. The reaction was quenched with water (25 ml) and the dichloromethane layer separated, dried (magnesium sulphate) and concentrated in vacuo. The residue was purified by flash column chromatography (SiO2) eluting with ethyl acetate/dichloromethane (1:10) to afford the title compound as a yellow oil (253 mg, 44%). HPLC retention time 4.4 min, Mass spectrum (ES+) m/z 319 (M+H).

후처리

  1. customThe reaction was quenched with water (25 ml)
  2. customthe dichloromethane layer separated
  3. dry with materialdried (magnesium sulphate)
  4. concentrationconcentrated in vacuo
  5. customThe residue was purified by flash column chromatography (SiO2)
  6. washeluting with ethyl acetate/dichloromethane (1:10)

출처 및 근거

ORD 기록
ord-274504934bfd4e96aa26c34146dfd17d
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08372840B2

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