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HCID 20207293, 화합물 → HCID 20207297, 화합물

HRID 542202
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HRID 542202 반응식
C([N:8](CC1C=CC=CC=1)[CH2:9][CH:10]([OH:25])[CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([CH2:18][N:19]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)[CH:13]=1)C1C=CC=CC=1>C(O)C.O.[Pd]>[NH3:8].[NH2:8][CH2:9][CH:10]([OH:25])[CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[C:14]([CH2:18][N:19]2[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24]2)[CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 1

HCID 20207293HCID 20207293, 화합물

생성물 2

HCID 222AmmoniaHCID 20207297HCID 20207297, 화합물수율 104.4%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 702Ethanol용매HCID 962Water용매

실험 절차

11.5 g (0.027 mol) of 1-dibenzylamino-3-[3-(1-piperidylmethyl)phenyl]-2-propanol in 90 ml of ethanol and 10 ml of water are hydrogenated at 35° C. and atmospheric pressure in the presence of 0.5 g of palladium/active charcoal (10% Pd). After removal of the catalyst by filtration and evaporation of the solvent, the residue consists of 5.8 g of a colourless oil which, after chromatographic purification with methanol/conc. ammonia (95:5), yields 3.5 g (52%) of the title compound in the form of a colourless oil. ##STR5##

후처리

  1. customare hydrogenated at 35° C.
  2. customAfter removal of the catalyst
  3. filtrationby filtration and evaporation of the solvent
  4. customafter chromatographic purification with methanol/conc

출처 및 근거

ORD 기록
ord-15f36f416fa14336a0512e96da173e26
출처 데이터셋
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04656180

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