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Ethanol → 2-(2-methoxyphenyl)thieno[3,2-d]pyrimidin-4(3H)-one

HRID 333701
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HRID 333701 반응식
[CH3:1][O:2][C:3]1[CH:19]=[CH:18][CH:17]=[CH:16][C:4]=1[C:5]([NH:7][C:8]1[CH:12]=[CH:11][S:10][C:9]=1[C:13]([NH2:15])=[O:14])=O.[OH-].[Na+].CCO>O>[CH3:1][O:2][C:3]1[CH:19]=[CH:18][CH:17]=[CH:16][C:4]=1[C:5]1[NH:15][C:13](=[O:14])[C:9]2[S:10][CH:11]=[CH:12][C:8]=2[N:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 590266413-(2-Methoxybenzamido)thiophene-2-carboxamide

생성물 1

HCID 1359915042-(2-methoxyphenyl)thieno[3,2-d]pyrimidin-4(3H)-one수율 62%

시약·촉매·용매 1

HCID 962Water용매

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온도
120 °C

실험 절차

A mixture of 3-(2-methoxybenzamido)thiophene-2-carboxamide (1.4 g, 5.0 mmol), 6 N aqueous NaOH (8 mL), and EtOH (8 mL) was heated at 120° C. for 16 h. The reaction was cooled, diluted with water, and extracted with CH2Cl2. The combined extracts were washed with water, dried over Na2SO4, and concentrated under vacuum to give 2-(2-methoxyphenyl)thieno[3,2-d]pyrimidin-4(3H)-one (0.80 g, 62% yield). LC/MS: m/z 259.3 (M+H)+ at 2.32 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).

후처리

  1. temperatureThe reaction was cooled
  2. extractionextracted with CH2Cl2
  3. washThe combined extracts were washed with water
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-a86392b889cb4a84acbf55a44e2eda64
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08883781B2

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