Hydrochloric Acid → ((S)-1-{(S)-2-[4-(4'-{[6-((2R,5S)-2,5-Dimethyl-piperazin-1-yl)-pyridine-3-carbonyl]-amino}-2'-trifluoromethoxy-biphenyl-4-yl)-1H-imidazol-2-yl]-pyrrolidine-1-carbonyl}-2-methyl-propyl)-carbamic acid methyl ester
Reaktionsgleichung
C(Cl)(=O)C.Cl.C(OC([N:13]1[CH2:18][C@@H:17]([CH3:19])[N:16]([C:20]2[CH:25]=[CH:24][C:23]([C:26](=[O:66])[NH:27][C:28]3[CH:33]=[CH:32][C:31]([C:34]4[CH:39]=[CH:38][C:37]([C:40]5[N:41]=[C:42]([C@@H:45]6[CH2:49][CH2:48][CH2:47][N:46]6[C:50](=[O:60])[C@@H:51]([NH:55][C:56]([O:58][CH3:59])=[O:57])[CH:52]([CH3:54])[CH3:53])[NH:43][CH:44]=5)=[CH:36][CH:35]=4)=[C:30]([O:61][C:62]([F:65])([F:64])[F:63])[CH:29]=3)=[CH:22][N:21]=2)[CH2:15][C@@H:14]1[CH3:67])=O)(C)(C)C>C(O)C>[CH3:59][O:58][C:56](=[O:57])[NH:55][C@H:51]([C:50]([N:46]1[CH2:47][CH2:48][CH2:49][C@H:45]1[C:42]1[NH:43][CH:44]=[C:40]([C:37]2[CH:38]=[CH:39][C:34]([C:31]3[CH:32]=[CH:33][C:28]([NH:27][C:26]([C:23]4[CH:22]=[N:21][C:20]([N:16]5[CH2:15][C@H:14]([CH3:67])[NH:13][CH2:18][C@H:17]5[CH3:19])=[CH:25][CH:24]=4)=[O:66])=[CH:29][C:30]=3[O:61][C:62]([F:65])([F:63])[F:64])=[CH:35][CH:36]=2)[N:41]=1)=[O:60])[CH:52]([CH3:53])[CH3:54]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Acetyl chloride (63.2 mL, 888 mmol) was added to ethanol (360 mL) and stirred at RT for 1 h. To the resulting HCl solution was added a solution of (2S,5R)-4-[5-(4′-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methyl-butyryl)-pyrrolidin-2-yl]-1H-imidazol-4-yl}-2-trifluoromethoxy-biphenyl-4-ylcarbamoyl)-pyridin-2-yl]-2,5-dimethyl-piperazine-1-carboxylic acid tert-butyl ester (73 g, 84 mmol) in ethanol (360 mL). The reaction mixture was stirred at RT overnight.
Aufarbeitung
- stirringThe reaction mixture was stirred at RT overnight
Quellen und Nachweise
- ORD-Eintrag
- ord-6246fbc25cae491dae68fa83c68292a1
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08883135B2
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