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Sulfuric Acid → 2-(5-Bromo-1-naphthalenyl)-1,6-dihydro-4-[(1-naphthalenyl)methyl]-6-oxo-5-pyrimidinecarbonitrile

HRID 2232060
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HRID 2232060 반응식
C[O-].[Na+].[Na].[C:5]([CH2:7][C:8]([NH2:10])=[O:9])#[N:6].CO[C:13](=[N:25][C:26]([C:28]1[C:37]2[C:32](=[C:33]([Br:38])[CH:34]=[CH:35][CH:36]=2)[CH:31]=[CH:30][CH:29]=1)=O)[CH2:14][C:15]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:18]=[CH:17][CH:16]=1.OS(O)(=O)=O>CO.O>[Br:38][C:33]1[CH:34]=[CH:35][CH:36]=[C:37]2[C:32]=1[CH:31]=[CH:30][CH:29]=[C:28]2[C:26]1[NH:10][C:8](=[O:9])[C:7]([C:5]#[N:6])=[C:13]([CH2:14][C:15]2[C:24]3[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=3)[CH:18]=[CH:17][CH:16]=2)[N:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 5

HCID 1118Sulfuric AcidHCID 7898CyanoacetamideHCID 5360545SodiumHCID 10942334Sodium MethoxideHCID 19863963Methyl-N-(5-bromo-1-naphthoyl)-2-(1-naphthalenyl)acetimidate

생성물 1

HCID 1358476532-(5-Bromo-1-naphthalenyl)-1,6-dihydro-4-[(1-naphthalenyl)methyl]-6-oxo-5-pyrimidinecarbonitrile
수율 71%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

To a stirred solution of sodium methoxide, freshly prepared from sodium (1.5 g, 0.065 mol) in methanol (75 mL), was added cyanoacetamide (4.2 g, 0.050 mol). After 2 minutes, methyl-N-(5-bromo-1-naphthoyl)-2-(1-naphthalenyl)acetimidate (21.6 g, 0.050 mol) was added. The resulting mixture was stirred at room temperature for 15 hours, then heated to reflux for 4 hours. After cooling to room temperature, the mixture was neutralized with H2SO4 (1.8 mL) and diluted with water. The product was collected by filtration, washed with water, and dried in vacuo to give a yellow solid (16.4 g, 71%), which was used without purification.

후처리

  1. temperatureheated
  2. temperatureto reflux for 4 hours
  3. temperatureAfter cooling to room temperature
  4. filtrationThe product was collected by filtration
  5. washwashed with water
  6. customdried in vacuo

출처 및 근거

ORD 기록
ord-c3cfdf489d0542219c8935832ac1528f
출처 데이터셋
uspto-grants-1988_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04786640

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