4-Fluorobenzenesulfonyl isocyanate → 1-{3-(7-Cyclopentyl-5-methyl-4-oxo-3,4-dihydroimidazo[5,1-f][1,2,4]-triazin-2-yl)-4-propoxyphenyl}-3-(4-fluorophenylsulfonyl)-urea
Reaktionsgleichung
[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([O:24][CH2:25][CH2:26][CH3:27])=[C:6]([C:8]2[NH:13][C:12](=[O:14])[C:11]3=[C:15]([CH3:23])[N:16]=[C:17]([CH:18]4[CH2:22][CH2:21][CH2:20][CH2:19]4)[N:10]3[N:9]=2)[CH:7]=1.[F:28][C:29]1[CH:34]=[CH:33][C:32]([S:35]([N:38]=[C:39]=[O:40])(=[O:37])=[O:36])=[CH:31][CH:30]=1>O1CCCC1>[CH:18]1([C:17]2[N:10]3[C:11]([C:12](=[O:14])[NH:13][C:8]([C:6]4[CH:7]=[C:2]([NH:1][C:39]([NH:38][S:35]([C:32]5[CH:33]=[CH:34][C:29]([F:28])=[CH:30][CH:31]=5)(=[O:36])=[O:37])=[O:40])[CH:3]=[CH:4][C:5]=4[O:24][CH2:25][CH2:26][CH3:27])=[N:9]3)=[C:15]([CH3:23])[N:16]=2)[CH2:22][CH2:21][CH2:20][CH2:19]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The preparation is carried out analogously to the procedure of example 54 using 150 mg (0.408 mmol) of the amino compound from example 44A and 411 mg (2.04 mmol) of 4-fluorobenzenesulfonyl isocyanate in 12 ml of tetrahydrofuran, which are reacted overnight.
Aufarbeitung
- customare reacted overnight
Quellen und Nachweise
- ORD-Eintrag
- ord-9b6acc6d97074603b60437d04dd0503a
- Quelldatensatz
- uspto-grants-2006_08
- Patentnummer
- US07098207B2
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