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4-Nitrobenzaldehyde → (3R,5S)-1-[(4-Nitrophenyl)methyl]-3,5-dimethylpiperazine

HRID 2424631
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HRID 2424631 반응식
[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[CH3:12][C@@H:13]1[CH2:18][NH:17][CH2:16][C@H:15]([CH3:19])[NH:14]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCCl.C(Cl)Cl>[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH2:8][N:17]2[CH2:16][C@H:15]([CH3:19])[NH:14][C@H:13]([CH3:12])[CH2:18]2)=[CH:6][CH:5]=1)([O-:3])=[O:2]
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참가 물질

6

반응물 3

HCID 5414-NitrobenzaldehydeHCID 5049666Sodium triacetoxyborohydrideHCID 6950261rel-(2R,6S)-2,6-dimethylpiperazine

생성물 1

HCID 59262210(3R,5S)-1-[(4-Nitrophenyl)methyl]-3,5-dimethylpiperazine수율 39.2%

시약·촉매·용매 2

HCID 111,2-Dichloroethane용매
HCID 6344
Dichloromethane
용매

실험 절차

A mixture of 4-nitrobenzaldehyde (6.612 g, 43.8 mmol) and (2R,6S)-2,6-dimethylpiperazine (5 g, 43.8 mmol) in 1,2-DCE (100 mL) was stirred at room temperature for 2 h. Sodium tri(acetoxy)borohydride (13.92 g, 65.7 mmol) was added and the reaction was stirred at room temperature over-weekend. The reaction mixture was diluted with DCM and washed with saturated aqueous NaHCO3 solution. The aqueous wash was extracted with 10% MeOH/DCM and the combined organics were dried and concentrated. Column chromatography eluting with 0-10% MeOH/DCM gave the title compound as a cream solid (4.278 g). δH (CDCl3, 400 MHz) 8.18 (2H, d), 7.51 (2H, d), 3.57 (2H, s), 2.97 (2H, m), 2.72 (2H, m), 1.72 (2H, m), 1.06 (6H, d). MS (ES+): MH+ 250.2.

후처리

  1. stirringthe reaction was stirred at room temperature over-weekend
  2. washwashed with saturated aqueous NaHCO3 solution
  3. washThe aqueous wash
  4. extractionwas extracted with 10% MeOH/DCM
  5. customthe combined organics were dried
  6. concentrationconcentrated
  7. washColumn chromatography eluting with 0-10% MeOH/DCM

출처 및 근거

ORD 기록
ord-429f271f18754f0ab5a3677a0b751574
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07964597B2

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