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1-Methylpiperazine → (2-Methoxy-3-nitro-phenyl)-(4-methyl-piperazin-1-yl)-methanone

HRID 1262309
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HRID 1262309 반응식
[CH3:1][O:2][C:3]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][CH:9]=[CH:8][C:4]=1[C:5]([OH:7])=O.[CH3:15][N:16]1[CH2:21][CH2:20][NH:19][CH2:18][CH2:17]1.O.ON1C2C=CC=CC=2N=N1.C([O-])(O)=O.[Na+]>CN(C)C=O>[CH3:1][O:2][C:3]1[C:11]([N+:12]([O-:14])=[O:13])=[CH:10][CH:9]=[CH:8][C:4]=1[C:5]([N:19]1[CH2:20][CH2:21][N:16]([CH3:15])[CH2:17][CH2:18]1)=[O:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 531671-MethylpiperazineHCID 516892Sodium BicarbonateHCID 27960291-Hydroxybenzotriazole hydrateHCID 120151952-Methoxy-3-nitrobenzoic acid

생성물 1

HCID 66712414(2-Methoxy-3-nitro-phenyl)-(4-methyl-piperazin-1-yl)-methanone수율 44%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

2-Methoxy-3-nitro-benzoic acid (1.20 g, 6.09 mmol), 1-Methylpiperazine (1.01 mL, 9.13 mmol) N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (1750 mg, 9.13 mmol, 1-hydroxybenzotriazole hydrate (1.45 g, 9.13 mmole) and N,N-Dimethylformamide (40.4 mL) were combined into a vial and stirred at room temperature for 1 hour. LCMS showed complete conversion to product. Diluted reaction mixture with saturated NaHCO3 and filtered off resulting ppt. The solid was filtered and washed with water. The solid was dried under vacuum overnight to give (2-Methoxy-3-nitro-phenyl)-(4-methyl-piperazin-1-yl)-methanone as a white solid (0.70 g, 44%)

후처리

  1. additionDiluted
  2. filtrationfiltered off
  3. customresulting ppt
  4. filtrationThe solid was filtered
  5. washwashed with water
  6. customThe solid was dried under vacuum overnight

출처 및 근거

ORD 기록
ord-c0a62e1f49304c1ea7042b99df886f66
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08471005B2

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