Reaktionsgleichung
[CH3:1][O:2][C:3]([C@@H:5]1[CH2:9][C@@H:8]([S:10]([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][C:14]=2[C:20]([F:23])([F:22])[F:21])(=[O:12])=[O:11])[CH2:7][N:6]1[C:24](=S)[CH2:25][C:26](=O)[CH3:27])=[O:4].Cl.[O:31]1[CH2:36][CH2:35][CH:34]([NH:37][NH2:38])[CH2:33][CH2:32]1>>[CH3:1][O:2][C:3]([C@@H:5]1[CH2:9][C@@H:8]([S:10]([C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][C:14]=2[C:20]([F:23])([F:21])[F:22])(=[O:11])=[O:12])[CH2:7][N:6]1[C:24]1[N:37]([CH:34]2[CH2:35][CH2:36][O:31][CH2:32][CH2:33]2)[N:38]=[C:26]([CH3:27])[CH:25]=1)=[O:4]Komponenten
3
Versuchsvorschrift
In analogy to the procedure described in example 192 h, (2S,4R)-4-(4-fluoro-2-trifluoromethyl-benzenesulfonyl)-1-(3-oxo-thiobutyryl)-pyrrolidine-2-carboxylic acid methyl ester (example 388 d) was reacted with (tetrahydro-pyran-4-yl)-hydrazine hydrochloride (CAS Reg. No. 116312-69-7) to give the title compound as brown solid. MS (ESI): m/z=520.3 [M+H]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-8dfdf928a1d948a1963c4d24d4e862fb
- Quelldatensatz
- uspto-grants-2012_04
- Patentnummer
- US08163793B2
Verknüpfte Notizen
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