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Triethylamine → 4-Benzyl-1-[2-(2-fluorophenyl)propanoyl]piperazine

HRID 1600837
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HRID 1600837 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]([CH3:12])[C:9]([OH:11])=O.[CH2:13]([N:20]1[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C(N(CC)CC)C.Cl.CN(C)CCCN=C=NCC>ClCCl>[CH2:13]([N:20]1[CH2:25][CH2:24][N:23]([C:9](=[O:11])[CH:8]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[F:1])[CH3:12])[CH2:22][CH2:21]1)[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
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참가 물질

6

반응물 4

HCID 8471TriethylamineHCID 759941-BenzylpiperazineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 184215882-(2-Fluoro-phenyl)-propionic acid

생성물 1

HCID 218308564-Benzyl-1-[2-(2-fluorophenyl)propanoyl]piperazine수율 38%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

2-(2-Fluorophenyl)propanoic acid (7.7 g, 0.046 mol), 1-benzylpiperazine (8.0 g, 0.045 mol), triethylamine (4.6 g, 0.046 mol) and 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride (9.6 g, 0.050 mol) were dissolved in dichloromethane (150 ml) and stirred at room temperature for 18 h. The solution was evaporated and the residue diluted with water and extracted with brine, dried and evaporated. Chromatography on silica gel with dichloromethane-methanol (97:3) yielded 4-benzyl-1-[2-(2-fluorophenyl)propanoyl]piperazine (5.54 g, 38%) as an oil.

후처리

  1. customThe solution was evaporated
  2. additionthe residue diluted with water
  3. extractionextracted with brine
  4. customdried
  5. customevaporated

출처 및 근거

ORD 기록
ord-170de012ad3c4b81969daf35188024b9
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05977116

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