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Phenyl isocyanate → 4-[N-methyl-N-(2-phenylethyl)amino]-1-anilinocarbonylpiperidine

HRID 962780
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인쇄 미리보기

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HRID 962780 반응식
[C:1]1([N:7]=[C:8]=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:10][N:11]([CH:20]1[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]1)[CH2:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C(Cl)(Cl)Cl>[CH3:10][N:11]([CH:20]1[CH2:21][CH2:22][N:23]([C:8]([NH:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[O:9])[CH2:24][CH2:25]1)[CH2:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7672Phenyl isocyanateHCID 10856966Methyl-phenethyl-piperidin-4-YL-amine

생성물 1

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

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

1.0 ml of phenyl 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-30ff3204a0b64769914115a267d09c51
출처 데이터셋
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05760058

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