Sodium Methoxide → Methyl 3-{4-hydroxy-6-oxo-2-[(E)-2-phenylethenyl]-1,6-dihydro-5-pyrimidinyl}propanoate

HRID 657111노트

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HRID 657111 반응식
[CH:1]([C:13]([O:15]C)=O)([C:9]([O:11]C)=O)[CH2:2][CH2:3][C:4]([O:6][CH2:7]C)=[O:5].[C:17]1(/[CH:23]=[CH:24]/[C:25](=[NH:27])[NH2:26])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.C[O-].[Na+]>CO>[OH:15][C:13]1[N:26]=[C:25](/[CH:24]=[CH:23]/[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[NH:27][C:9](=[O:11])[C:1]=1[CH2:2][CH2:3][C:4]([O:6][CH3:7])=[O:5]

참가 물질

5

실험 절차

3-Ethyl 1,1-dimethyl 1,1,3-propanetricarboxylate (23.8 g; 103 mmol) and (2E)-3-phenyl-2-propenimidamide (10.0 g; 68.4 mmol) were combined in MeOH (400 mL), treated with NaOMe in MeOH (31.0 g; 143 mmol) and the solution was stirred at room temperature for 2 days. The solution turned dark, and a dark green solid was filtered off. The solution was concentrated under vacuum, diluted with water, acidified to pH 2 with 6N HCl and the resulting yellow precipitate was filtered off. The aqueous mother liquor was extracted with EtOAc. During the extraction more yellow precipitate formed and was collected. The combined yellow solids were dried under vacuum and used without further purification (12.1 g, 59%).

후처리

  1. filtrationa dark green solid was filtered off
  2. concentrationThe solution was concentrated under vacuum
  3. additiondiluted with water
  4. filtrationthe resulting yellow precipitate was filtered off
  5. extractionThe aqueous mother liquor was extracted with EtOAc
  6. extractionDuring the extraction more yellow precipitate
  7. customformed
  8. customwas collected
  9. customThe combined yellow solids were dried under vacuum
  10. customused without further purification (12.1 g, 59%)

출처 및 근거

ORD 기록
ord-71e87ad73dd84ac9a75668d9799b6a0f
출처 데이터셋
uspto-grants-2011_12
특허 번호
US08071592B2

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