Methanesulfonyl chloride → HCID 69100720, Verbindung
Reaktionsgleichung
Cl.Cl.[NH2:3][C:4]1[CH:5]=[C:6]([NH:10][C:11](=[O:27])[CH2:12][N:13]2[CH2:18][CH2:17][CH:16]([CH2:19][C:20]3[CH:25]=[CH:24][C:23]([F:26])=[CH:22][CH:21]=3)[CH2:15][CH2:14]2)[CH:7]=[CH:8][CH:9]=1.[CH3:28][S:29]([Cl:32])(=[O:31])=[O:30]>C(OC(=O)C)C.C(OCC)C>[F:26][C:23]1[CH:24]=[CH:25][C:20]([CH2:19][CH:16]2[CH2:15][CH2:14][N:13]([CH2:12][C:11]([NH2:10])=[O:27])[CH2:18][CH2:17]2)=[CH:21][CH:22]=1.[ClH:32].[CH3:28][S:29]([NH:3][C:4]1[CH:5]=[C:6]([NH:10][C:11](=[O:27])[CH3:12])[CH:7]=[CH:8][CH:9]=1)(=[O:31])=[O:30]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The title compound is prepared from N-(3-amino-phenyl)-2-[4-(4-fluoro-benzyl)-piperidin-1-yl]-acetamide dihydrochloride (Example 183) and methanesulfonyl chloride according to the method described in Example 176. Melting Point: 85-90° C. (dec.) (diethylether- ethyl acetate)
Quellen und Nachweise
- ORD-Eintrag
- ord-d7ecd144e5454f7e9c6acb566533a607
- Quelldatensatz
- uspto-grants-2008_10
- Patentnummer
- US07435744B2
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