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Potassium Carbonate → 2-[4-(6-Methoxy-quinazolin-4-yloxymethyl)-cyclohexylamino]-N-pyridin-2-yl-acetamide

HRID 1354226
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HRID 1354226 반응식
Br[CH2:2][C:3]([NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][N:7]=1)=[O:4].C(=O)([O-])[O-].[K+].[K+].[CH3:18][O:19][C:20]1[CH:21]=[C:22]2[C:27](=[CH:28][CH:29]=1)[N:26]=[CH:25][N:24]=[C:23]2[O:30][CH2:31][CH:32]1[CH2:37][CH2:36][CH:35]([NH2:38])[CH2:34][CH2:33]1>CN(C=O)C>[CH3:18][O:19][C:20]1[CH:21]=[C:22]2[C:27](=[CH:28][CH:29]=1)[N:26]=[CH:25][N:24]=[C:23]2[O:30][CH2:31][CH:32]1[CH2:37][CH2:36][CH:35]([NH:38][CH2:2][C:3]([NH:5][C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][N:7]=2)=[O:4])[CH2:34][CH2:33]1
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 34158372-bromo-N-pyridin-2-yl-acetamideHCID 211046334-(6-Methoxyquinazolin-4-yloxymethyl)-cyclohexylamine

생성물 1

HCID 211045902-[4-(6-Methoxy-quinazolin-4-yloxymethyl)-cyclohexylamino]-N-pyridin-2-yl-acetamide

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2-Bromo-N-pyridin-2-yl-acetamide (0.075 g, 0.35 mmol) and potassium carbonate (0.054 g, 0.39 mmol) were added to a solution of 4-(6-methoxy-quinazolin-4-yloxymethyl)-cyclohexylamine (0.1 g, 0.35 mmol) in DMF (3.5 ml). The reaction mixture was stirred at room temperature for 2 days and then concentrated to dryness by rotary evaporation. The residue was purified by column chromatography on silica gel (dichloromethane/MeOH 19/1 1% NH4OH).

후처리

  1. concentrationconcentrated to dryness by rotary evaporation
  2. customThe residue was purified by column chromatography on silica gel (dichloromethane/MeOH 19/1 1% NH4OH)

출처 및 근거

ORD 기록
ord-8af410ff42844fe3b9e6150895ae0bf7
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07223776B2

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