3-Methylisoxazole-5-carboxylic acid → HCID 178427116, Verbindung
Reaktionsgleichung
Cl.Cl.[O:3]1[C:7]2[CH:8]=[CH:9][CH:10]=[C:11]([CH:12]3[CH2:17][CH2:16][N:15]([CH2:18][CH2:19][C@H:20]4[CH2:25][CH2:24][C@H:23]([NH2:26])[CH2:22][CH2:21]4)[CH2:14][CH2:13]3)[C:6]=2[CH2:5][CH2:4]1.[CH3:27][C:28]1[CH:32]=[C:31]([C:33](O)=[O:34])[O:30][N:29]=1>>[O:3]1[C:7]2[CH:8]=[CH:9][CH:10]=[C:11]([CH:12]3[CH2:17][CH2:16][N:15]([CH2:18][CH2:19][C@H:20]4[CH2:21][CH2:22][C@H:23]([NH:26][C:33]([C:31]5[O:30][N:29]=[C:28]([CH3:27])[CH:32]=5)=[O:34])[CH2:24][CH2:25]4)[CH2:14][CH2:13]3)[C:6]=2[CH2:5][CH2:4]1Komponenten
3
Versuchsvorschrift
The title compound, off-white solid (89 mg, 82%), MS (ISP) m/z=438.3 [(M+H)+], mp 215° C., was prepared in accordance with the general method of example 1 from trans-4-{2-[4-(2,3-dihydro-benzofuran-4-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine dihydrochloride (intermediate B) (100 mg, 0.25 mmol) and 3-methyl-isoxazole-5-carboxylic acid.
Quellen und Nachweise
- ORD-Eintrag
- ord-192dfa1c0e0c446fa3ecfae7fe6cfdb1
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08877778B2
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