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Formaldehyde → 6-(Ethoxymethyl-amino)-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide

HRID 2080216
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HRID 2080216 반응식
[NH2:1][C:2]1[CH:23]=[CH:22][C:5]([C:6]([NH:8][CH2:9][C:10]2[S:11][C:12]([O:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[CH:13][CH:14]=2)=[O:7])=[CH:4][N:3]=1.C=O.O.[C:27]([O:30][CH2:31]C)(=O)[CH3:28]>C(O)C>[CH2:27]([O:30][CH2:31][NH:1][C:2]1[CH:23]=[CH:22][C:5]([C:6]([NH:8][CH2:9][C:10]2[S:11][C:12]([O:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[CH:13][CH:14]=2)=[O:7])=[CH:4][N:3]=1)[CH3:28]
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참가 물질

6

반응물 4

HCID 712FormaldehydeHCID 962WaterHCID 8857Ethyl AcetateHCID 231305396-Amino-N-(5-phenoxy thiophen-2-ylmethyl)-nicotinamide

생성물 1

HCID 231303456-(Ethoxymethyl-amino)-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide수율 66.1%

시약·촉매·용매 1

HCID 702
Ethanol
용매

실험 절차

To a solution of 6-amino-N-(5-phenoxy-thiophen-2-ylmethyl)-nicotinamide described in Example A-138 (600 mg, 1.8 mmol) in ethanol (40 mL) were added 5,5-dimethylimidazo phospho-2,4-dione (260 mg, 2.0 mmol) and 37% formaldehyde aqueous solution (3 mL), and the solution was stirred under reflux for 30 minutes. Water and ethyl acetate were added to the reaction solution, which was then partitioned, and the organic layer was washed with water twice. NH silica gel was added to the organic layer, the solvent was evaporated in vacuo for adsorption, purification was carried out by NH silica gel column chromatography (ethyl acetate), and the title compound (457 mg, 1.19 mmol, 66.1%) was obtained as a white solid.

후처리

  1. temperatureunder reflux for 30 minutes
  2. customwas then partitioned
  3. washthe organic layer was washed with water twice
  4. additionNH silica gel was added to the organic layer
  5. customthe solvent was evaporated in vacuo for adsorption, purification

출처 및 근거

ORD 기록
ord-11150e20e3e34ac6920922d18ceb38d8
출처 데이터셋
uspto-grants-2011_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07932272B2

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