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(4aS,8aS)-1-benzyl-4-(phenylamino)octahydroquinolin-4a(2H)-ol → HCID 68154084, 화합물

HRID 73614
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인쇄 미리보기

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HRID 73614 반응식
C([N:8]1[C@@H:17]2[C@:12]([OH:18])([CH2:13][CH2:14][CH2:15][CH2:16]2)[CH:11]([NH:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH2:10][CH2:9]1)C1C=CC=CC=1>CO.[Pd]>[C:20]1([NH:19][CH:11]2[C@:12]3([OH:18])[C@H:17]([CH2:16][CH2:15][CH2:14][CH2:13]3)[NH:8][CH2:9][CH2:10]2)[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 52911548(4aS,8aS)-1-benzyl-4-(phenylamino)octahydroquinolin-4a(2H)-ol

생성물 1

HCID 68154084HCID 68154084, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

반응 조건

온도
60 °C

실험 절차

To a mixture of (4aS,8aS)-1-benzyl-4-(phenylamino)octahydroquinolin-4a(2H)-ol (0.280 g, 0.832 mmol) in MeOH (5 mL) was added NH4COOH (0.840 g, 13.3 mmol) and 10% Pd/C (0.280 g). The resulting mixture was heated at 60° C. for several hours. The reaction was cooled to rt, filtered through a syringe filter, washed with EtOH, and concentrated to give the title compound. LRMS M+H calc'd: 247.34. found 247.34

후처리

  1. temperatureThe reaction was cooled to rt
  2. filtrationfiltered through a syringe
  3. filtrationfilter
  4. washwashed with EtOH
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-4f198c0a3a474dfe812baf3eda919d30
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08829196B2

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