5-Aminoimidazole-4-carboxamide hydrochloride → 4-(3,4-Dimethoxyphenyl)imidazo[1,5-a]pyrimidine-8-carboxamide

HRID 1199946Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1199946
C[N:2]([CH3:17])[CH:3]=[CH:4][C:5]([C:7]1[CH:12]=[CH:11][C:10]([O:13][CH3:14])=[C:9]([O:15][CH3:16])[CH:8]=1)=O.Cl.NC1[N:21]=[CH:22][NH:23][C:24]=1[C:25]([NH2:27])=[O:26].C(=O)(O)[O-].[Na+]>C(O)(=O)C>[CH3:16][O:15][C:9]1[CH:8]=[C:7]([C:5]2[N:21]3[CH:22]=[N:23][C:24]([C:25]([NH2:27])=[O:26])=[C:17]3[N:2]=[CH:3][CH:4]=2)[CH:12]=[CH:11][C:10]=1[O:13][CH3:14]

Komponenten

5

Versuchsvorschrift

A stirred mixture of 15.0 g of 3-dimethylamino-3',4'-dimethoxyacrylophenone (prepared as described in Example 6) and 8.0 g of 4-amino-5-imidazolecarboxamide hydrochloride in 150 ml of glacial acetic acid was heated at reflux for 24 hours. The solvent was evaporated in vacuo to give an oil. The oil solidified on standing at room temperature. The solid was treated with 200 ml of saturated sodium bicarbonate solution and then filtered to collect the crystals. The material was treated by boiling with 700 ml of ethanol and then was filtered. The solid was recrystallized from methanol-chloroform to give 7.9 g of the desired product, mp 262°-265° C.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureat reflux for 24 hours
  3. customThe solvent was evaporated in vacuo
  4. customto give an oil
  5. customon standing at room temperature
  6. filtrationfiltered
  7. customto collect the crystals
  8. additionThe material was treated
  9. filtrationwas filtered
  10. customThe solid was recrystallized from methanol-chloroform

Quellen und Nachweise

ORD-Eintrag
ord-64ed4a5eceae4ba185a46e65de2291fa
Quelldatensatz
uspto-grants-1990_02
Patentnummer
US04904658

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