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4-(4-Methylbenzyl)-piperidin-4-ol → (RS)-1-(6-methoxy-2,3-dihydro-benzofuran-2-ylmethyl)-4-(4-methyl-benzyl)-piperidin-4-ol

HRID 278446
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인쇄 미리보기

반응식

HRID 278446 반응식
[CH3:1][O:2][C:3]1[CH:23]=[CH:22][C:6]2[CH2:7][CH:8]([CH2:10]OS(C3C=CC(C)=CC=3)(=O)=O)[O:9][C:5]=2[CH:4]=1.[CH3:24][C:25]1[CH:38]=[CH:37][C:28]([CH2:29][C:30]2([OH:36])[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]2)=[CH:27][CH:26]=1>CN(C=O)C>[CH3:1][O:2][C:3]1[CH:23]=[CH:22][C:6]2[CH2:7][CH:8]([CH2:10][N:33]3[CH2:34][CH2:35][C:30]([CH2:29][C:28]4[CH:27]=[CH:26][C:25]([CH3:24])=[CH:38][CH:37]=4)([OH:36])[CH2:31][CH2:32]3)[O:9][C:5]=2[CH:4]=1
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참가 물질

4

반응물 2

HCID 105362424-(4-Methylbenzyl)-piperidin-4-olHCID 54378120(RS)-toluene-4-sulfonic acid 6-methoxy-2,3-dihydro-benzofuran-2-ylmethyl ester

생성물 1

HCID 22628365(RS)-1-(6-methoxy-2,3-dihydro-benzofuran-2-ylmethyl)-4-(4-methyl-benzyl)-piperidin-4-ol수율 66%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
130 °C

실험 절차

(RS)-toluene-4-sulfonic acid 6-methoxy-2,3-dihydro-benzofuran-2-ylmethyl ester (110 mg, 0.33 mmol) and 4-(4-methyl-benzyl)-piperidin-4-ol (148 mg, 0.72 mmol) were dissolved in DMF (3 ml) and heated at 130° C. for 1 h. DMF was then evaporated, the residue was dissolved in CH2Cl2 (5 ml) and washed with H2O (5 ml). Organic phase was dried over Na2SO4, and concentrated. The residue was chromatographed over SiO2 (Merck 230-400 mesh) eluting with CH2Cl2-MeOH(19:1) to provide (RS)-1-(6-methoxy-2,3-dihydro-benzofuran-2-ylmethyl)-4-(4-methyl-benzyl)-piperidin-4-ol (80 mg, 66%) as a yellow oil, MS:m/e=368.4 (M+H+).

후처리

  1. customDMF was then evaporated
  2. dissolutionthe residue was dissolved in CH2Cl2 (5 ml)
  3. washwashed with H2O (5 ml)
  4. dry with materialOrganic phase was dried over Na2SO4
  5. concentrationconcentrated
  6. customThe residue was chromatographed over SiO2 (Merck 230-400 mesh)
  7. washeluting with CH2Cl2-MeOH(19:1)

출처 및 근거

ORD 기록
ord-8c4f294590064ef89c266db3166a678a
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06359138B1

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