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Methyl-phenethyl-piperidin-4-YL-amine → 4-[N-methyl-N-(2-phenylethyl)amino]-1-anilinocarbonylpiperidine

HRID 2257142
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HRID 2257142 반응식
[N-:1]=[C:2]=[O:3].[C:4]1(O)[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:11][N:12]([CH:21]1[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]1)[CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C(Cl)(Cl)Cl>[CH3:11][N:12]([CH:21]1[CH2:22][CH2:23][N:24]([C:2]([NH:1][C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=2)=[O:3])[CH2:25][CH2:26]1)[CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 10856966Methyl-phenethyl-piperidin-4-YL-amineHCID 18798726Phenol isocyanate

생성물 1

HCID 232850024-[N-methyl-N-(2-phenylethyl)amino]-1-anilinocarbonylpiperidine

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

1.0 ml of phenol isocyanate was added to a solution of 1.0 g of 4-[N-methyl-N-(2-phenylethyl)amino]piperidine in 15 ml of chloroform. The mixture was stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure. To the residue was added diethyl ether for crystallization. The resulting crystals were collected by filtration and recrystallized from ethyl acetate to obtain 0.7 g of 4-[N-methyl-N-(2-phenylethyl)amino]-1-anilinocarbonylpiperidine as colorless prism-like crystals.

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionTo the residue was added diethyl ether
  3. customfor crystallization
  4. filtrationThe resulting crystals were collected by filtration
  5. customrecrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-02c573fccbbc4127a963d6a2ea3d8016
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05656642

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