Methyl Isocyanate → 4-(5-Chloro-3-methylcarbamoylspiro[indan-1,3'-pyrrolidin]-1'-yl)-p-fluorobutyrophenone
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]2[C:24](=[CH:25][CH:26]=1)[C:7]1([CH2:11][CH2:10][N:9]([CH2:12][CH2:13][CH2:14][C:15]([C:17]3[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=3)=[O:16])[CH2:8]1)[CH2:6][CH:5]2O.[CH3:28][N:29]=[C:30]=[O:31].C(O)(=O)/C=C/C([O-])=O>C(Cl)(Cl)Cl>[Cl:1][C:2]1[CH:3]=[C:4]2[C:24](=[CH:25][CH:26]=1)[C:7]1([CH2:11][CH2:10][N:9]([CH2:12][CH2:13][CH2:14][C:15]([C:17]3[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=3)=[O:16])[CH2:8]1)[CH2:6][CH:5]2[C:30](=[O:31])[NH:29][CH3:28]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
4-(5-Chloro-3-hydroxyspiro[indan-1,3'-pyrrolidin]-1'-yl)-p-fluorobutyrophenone is reacted with methyl isocyanate in chloroform in a manner analogous to that described in Example 19. Reaction time 24 hours at the boil. The hydrogen fumarate of the title compound has a M.P. of 151°-153° (from ethanol/ether).
Aufarbeitung
- customReaction time 24 hours at the boil
Quellen und Nachweise
- ORD-Eintrag
- ord-57fbfc9afb22456286dfbd33ea3257ea
- Quelldatensatz
- uspto-grants-1976_05
- Patentnummer
- US03958003
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