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2-(5-(Benzyloxy)-3H-imidazo[4,5-b]pyridin-3-yl)cyclohexanone → HCID 178515950, 화합물

HRID 1890290
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HRID 1890290 반응식
C([O:8][C:9]1[N:14]=[C:13]2[N:15]([CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][C:19]3=[O:24])[CH:16]=[N:17][C:12]2=[CH:11][CH:10]=1)C1C=CC=CC=1>C(O)C.[Pd]>[OH:8][C:9]1[N:14]=[C:13]2[N:15]([CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][C:19]3=[O:24])[CH:16]=[N:17][C:12]2=[CH:11][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 673135802-(5-(Benzyloxy)-3H-imidazo[4,5-b]pyridin-3-yl)cyclohexanone

생성물 1

HCID 178515950HCID 178515950, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

2-(5-(Benzyloxy)-3H-imidazo[4,5-b]pyridin-3-yl)cyclohexanone (0.400 g, 1.25 mmol), was taken up in ethanol (5 mL). Catalytic palladium on carbon was added, and the solution was placed under an atmosphere of hydrogen and stirred at room temperature for 2 days. The solution was then filtered through Celite®. The solvent was removed under reduced pressure and the residue was purified by preparative HPLC to give the title compound. LCMS m/z=232.1 [M+H]+; 1H NMR (400 MHz, CDCl3) δ ppm 1.80-1.95 (m, 1H), 1.95-2.10 (m, 1H), 2.15-2.35 (m, 4H), 2.70-2.50 (m, 2H), 4.50 (dd, J1=13.2 Hz, J2=5.7 Hz, 1H), 6.89 (d, J=8.9 Hz, 1H), 8.16 (d, J=8.9 Hz, 1H), 8.74 (s, 1H).

후처리

  1. filtrationThe solution was then filtered through Celite®
  2. customThe solvent was removed under reduced pressure
  3. customthe residue was purified by preparative HPLC

출처 및 근거

ORD 기록
ord-073f4f72ca4f4296a8c5d2ca80d5f62c
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507473B2

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