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Ethanol → 2-Isopropyl-5-phenyl-3H-thieno[2,3-d]pyrimidin-4-one

HRID 910184
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인쇄 미리보기

반응식

HRID 910184 반응식
C(O[C:4]([C:6]1[C:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:9][S:8][C:7]=1[NH2:17])=[O:5])C.Cl.[CH:19]([CH2:22][C:23]([NH2:25])=N)(C)C.[CH2:26](O)C>>[CH:22]([C:23]1[NH:25][C:4](=[O:5])[C:6]2[C:10]([C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=3)=[CH:9][S:8][C:7]=2[N:17]=1)([CH3:19])[CH3:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 73242Ethyl 2-amino-4-phenylthiophene-3-carboxylateHCID 189679323-Methylbutanimidamide hydrochloride

생성물 1

HCID 288680672-Isopropyl-5-phenyl-3H-thieno[2,3-d]pyrimidin-4-one

실험 절차

A stirred mixture of 2-amino-4-phenylthiophene-3-carboxylic acid ethyl ester (350.43 g, 1.54 mol), isopropylacetamidine hydrochloride (958.75 g, 7.7 mol) and ethanol (1500 ml) was heated under reflux for 18 hours then allowed to cool to ambient temperature. The resulting solid was collected by filtration, washed with a little cold ethanol, then crystallised from ethanol to give 2-Isopropyl-5-phenyl-3H-thieno[2,3-d]pyrimidin-4-one as a yellow solid which was used without further purification.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 18 hours
  3. filtrationThe resulting solid was collected by filtration
  4. washwashed with a little cold ethanol
  5. customcrystallised from ethanol

출처 및 근거

ORD 기록
ord-f133ed69a02a4fd199475b57d66357f8
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08022076B2

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