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(S)-2-(2-isopropoxy-3-methylphenyl)-1-(4-pyridinyl)ethanol → (S)-2-(2-isopropoxy-3-methylphenyl)-1-(4-piperidinyl)ethanol

HRID 2074415
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인쇄 미리보기

반응식

HRID 2074415 반응식
[CH:1]([O:4][C:5]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:6]=1[CH2:12][C@@H:13]([C:15]1[CH:20]=[CH:19][N:18]=[CH:17][CH:16]=1)[OH:14])([CH3:3])[CH3:2]>O=[Pt]=O.CC(O)=O>[CH:1]([O:4][C:5]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:6]=1[CH2:12][C@@H:13]([CH:15]1[CH2:16][CH2:17][NH:18][CH2:19][CH2:20]1)[OH:14])([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 58870080(S)-2-(2-isopropoxy-3-methylphenyl)-1-(4-pyridinyl)ethanol

생성물 1

HCID 58870110(S)-2-(2-isopropoxy-3-methylphenyl)-1-(4-piperidinyl)ethanol

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 176Acetic Acid용매

실험 절차

Shake a mixture of (S)-2-(2-isopropoxy-3-methylphenyl)-1-(4-pyridinyl)ethanol (21.1 g, 78 mmol), HOAc (400 mL) and PtO2 (370 mg) with H2 (50 psi) for 15 hr. Filter the mixture through celite and evaporate the solvent to give (S)-2-(2-isopropoxy-3-methylphenyl)-1-(4-piperidinyl)ethanol as the acetate salt; 1H-NMR (CDCl3) δ 7.1-6.9 (m, 2H), 4.2 (m, 1H), 3.6 (m, 1H), 3.4 (m, 2H), 2.9-2.7 (m, 4H), 2.3 (s, 3H), 2.0 (s, 3H), 2.1-1.5 (m, 5H), 1.3 (d, 6H).

후처리

  1. filtrationFilter the mixture through celite
  2. customevaporate the solvent

출처 및 근거

ORD 기록
ord-3131b9ce416f45ffab58679eb0ab5474
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07919508B2

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