ethyl 4-amino-1H-imidazole-5-carboxylate → Ethyl 4-(2-thienyl)imidazo[1,5-a]pyrimidine-8carboxylate

HRID 1758797

반응식

HRID 1758797 반응식
[NH2:1][C:2]1[N:3]=[CH:4][NH:5][C:6]=1[C:7]([O:9][CH2:10][CH3:11])=[O:8].CN(C)[CH:14]=[CH:15][C:16]([C:18]1[S:19][CH:20]=[CH:21][CH:22]=1)=O>C(O)(=O)C>[S:19]1[CH:20]=[CH:21][CH:22]=[C:18]1[C:16]1[N:3]2[CH:4]=[N:5][C:6]([C:7]([O:9][CH2:10][CH3:11])=[O:8])=[C:2]2[N:1]=[CH:14][CH:15]=1

참가 물질

4

반응물 2

HCID 343359ethyl 4-amino-1H-imidazole-5-carboxylateHCID 6023993-(Dimethylamino)-1-(2-thienyl)-2-propen-1-one

생성물 1

HCID 20508943Ethyl 4-(2-thienyl)imidazo[1,5-a]pyrimidine-8carboxylate

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 1.55 g. (0.01 mols) of ethyl 4-amino-5-imidazolecarboxylate and 1.81 g. (0.01 mols) of 3-dimethylamino-1-(2-thienyl)-2-propen-1-one (prepared as described in Example 1, Part A) in 25 ml. of glacial acetic acid can be refluxed for 16 hours, then cooled and evaporated to dryness in vacuo. The residue can be dissolved in dichloromethane and passed through a short column of hydrous magnesium silicate. The effluent can be refluxed on a steam bath with a slow constant addition of n-hexane. At the first appearance of crystallization, heating should be curtailed and the solution allowed to cool. The precipitated material can be collected by filtration to produce ethyl 4-(2-thienyl)imidazo[1,5-a]pyrimidine-8carboxylate.

후처리

  1. additionA mixture of 1.55 g
  2. temperaturecooled
  3. customevaporated to dryness in vacuo
  4. dissolutionThe residue can be dissolved in dichloromethane
  5. temperatureThe effluent can be refluxed on a steam bath with a slow constant addition of n-hexane
  6. customAt the first appearance of crystallization
  7. temperatureheating should
  8. temperatureto cool
  9. filtrationThe precipitated material can be collected by filtration

출처 및 근거

ORD 기록
ord-32b07c49195d4ad6be6067c3e13a9c5c
출처 데이터셋
uspto-grants-1983_02
특허 번호
US04374988

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