4-Isoxazolecarboxylic acid, 3-(2,6-dichlorophenyl)-5-methyl- → 3-(2,6-Dichlorophenyl)-5-methyl-N-[3-[4-[2-(2,2,2-trifluoroethoxy)phenyl]-1-piperazinyl]pro-pyl]isoxazole-4-carboxamide
Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:13]([C:14]([OH:16])=O)=[C:12]([CH3:17])[O:11][N:10]=1.[NH2:18][CH2:19][CH2:20][CH2:21][N:22]1[CH2:27][CH2:26][N:25]([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=2[O:34][CH2:35][C:36]([F:39])([F:38])[F:37])[CH2:24][CH2:23]1>>[Cl:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[C:3]=1[C:9]1[C:13]([C:14]([NH:18][CH2:19][CH2:20][CH2:21][N:22]2[CH2:23][CH2:24][N:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[O:34][CH2:35][C:36]([F:38])([F:39])[F:37])[CH2:26][CH2:27]2)=[O:16])=[C:12]([CH3:17])[O:11][N:10]=1Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
The title compound was synthesised according to the procedure described in Example 1 but using 3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxylic acid instead of 3-phenyl-5-methyliso-xazole-4-carboxylic acid and Compound 12B instead of Compound 1B. Extraction with diethyl ether followed by purification by flash chromatography (chloroform-2 N ammonia in methanol 100:3) afforded the title compound (75%) as an oil.
Aufarbeitung
- customThe title compound was synthesised
- extractionExtraction with diethyl ether
- customfollowed by purification by flash chromatography (chloroform-2 N ammonia in methanol 100:3)
Quellen und Nachweise
- ORD-Eintrag
- ord-3d450bbece5e49838d63b4b72ec67029
- Quelldatensatz
- uspto-grants-2004_01
- Patentnummer
- US06680319B2
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