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3-(4-benzyloxy-benzyl)-6-(1-methyl-1H-pyrazol-4-yl)-imidazo[1,2-b]pyridazine → HCID 44206066, 화합물

HRID 69159
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HRID 69159 반응식
C([O:8][C:9]1[CH:30]=[CH:29][C:12]([CH2:13][C:14]2[N:18]3[N:19]=[C:20]([C:23]4[CH:24]=[N:25][N:26]([CH3:28])[CH:27]=4)[CH:21]=[CH:22][C:17]3=[N:16][CH:15]=2)=[CH:11][CH:10]=1)C1C=CC=CC=1>[Pd].C(O)C>[CH3:28][N:26]1[CH:27]=[C:23]([C:20]2[CH:21]=[CH:22][C:17]3[N:18]([C:14]([CH2:13][C:12]4[CH:11]=[CH:10][C:9]([OH:8])=[CH:30][CH:29]=4)=[CH:15][N:16]=3)[N:19]=2)[CH:24]=[N:25]1
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참가 물질

4

반응물 1

HCID 686333193-(4-benzyloxy-benzyl)-6-(1-methyl-1H-pyrazol-4-yl)-imidazo[1,2-b]pyridazine

생성물 1

HCID 44206066HCID 44206066, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

10% Palladium on carbon (49 mg) was added to a solution of 3-(4-benzyloxy-benzyl)-6-(1-methyl-1H-pyrazol-4-yl)-imidazo[1,2-b]pyridazine (Stage 5.1, 214 mg, 0.46 mmol) in ethanol and the resulting mixture was stirred under an atmosphere of hydrogen at rt for 24 h. The RM was filtered through Celite and concentrated in vacuo. Purification by HPLC afforded the title compound as a white solid (tR 0.8 min (conditions 2), MH+=306, 1H-NMR in CD3OD: 8.4 (s, 1H), 8.2 (d, 1H), 8.1 (s, 1H), 8.0 (d, 1H), 7.7 (s, 1H), 7.2 (d, 2H), 6.8 (d, 2H), 4.3 (s, 2H), 4.0 (s, 3H)).

후처리

  1. filtrationThe RM was filtered through Celite
  2. concentrationconcentrated in vacuo
  3. customPurification by HPLC

출처 및 근거

ORD 기록
ord-f3b8706cfaca4f5591e80e5db4cc0333
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08822468B2

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