Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:11]=[C:10]([S:12]([Cl:15])(=[O:14])=[O:13])[CH:9]=[CH:8][C:4]=1[C:5](O)=O.[NH2:16][C:17]1[C:22]([NH2:23])=[CH:21][N:20]=[CH:19][N:18]=1>>[ClH:15].[CH3:1][O:2][C:3]1[CH:11]=[C:10]([S:12]([Cl:15])(=[O:14])=[O:13])[CH:9]=[CH:8][C:4]=1[C:5]1[N:16]=[C:17]2[C:22]([NH:23][CH:19]=[N:18]2)=[CH:21][N:20]=1Komponenten
3
Versuchsvorschrift
Prepared analogously to Example C from 2.5 gm of 2-methoxy-4-chlorosulfonyl benzoic acid and 2.4 gm of 4,5-diamino-pyrimidine (crystalline product obtained from dihydrochloride and 1 mol of common salt) by refluxing for eight hours. The solid crude product was processed further without any purification.
Aufarbeitung
- temperatureby refluxing for eight hours
- customThe solid crude product was processed further without any purification
Quellen und Nachweise
- ORD-Eintrag
- ord-960828db7cb74670a598895fc7b94ba4
- Quelldatensatz
- uspto-grants-1987_09
- Patentnummer
- US04696931
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