Hydrochloric Acid → 3-[(1-Cyano-4-hydroxy-7-phenethyl-isoquinoline-3-carbonyl)-amino]-2,2-dimethyl-propionic acid
Reaktionsgleichung
C[O:2][C:3](=[O:32])[C:4]([CH3:31])([CH3:30])[CH2:5][NH:6][C:7]([C:9]1[N:10]=[C:11]([C:28]#[N:29])[C:12]2[C:17]([C:18]=1[OH:19])=[CH:16][CH:15]=[C:14]([CH2:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[CH:13]=2)=[O:8].[OH-].[Na+].Cl>CO>[C:28]([C:11]1[C:12]2[C:17](=[CH:16][CH:15]=[C:14]([CH2:20][CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[CH:13]=2)[C:18]([OH:19])=[C:9]([C:7]([NH:6][CH2:5][C:4]([CH3:31])([CH3:30])[C:3]([OH:32])=[O:2])=[O:8])[N:10]=1)#[N:29]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 3-[(1-cyano-4-hydroxy-7-phenethyl-isoquinoline-3-carbonyl)-amino]-2,2-dimethyl-propionic acid methyl ester (55 mg, 0.13 mmol), 2 M NaOH (2 mL) and MeOH (2 mL) was stirred at r.t. for 3 h. 1 M HCl was added until pH was ˜2, and the resulting suspension was extracted with EtOAc. The organic layer was dried over MgSO4 and concentrated. The crude product was purified by column chromatography (0-30% EtOAc/hexanes+2% AcOH) to give 38 mg of the title compound. MS: (−) m/z 416.14 (M−1).
Aufarbeitung
- extractionthe resulting suspension was extracted with EtOAc
- dry with materialThe organic layer was dried over MgSO4
- concentrationconcentrated
- customThe crude product was purified by column chromatography (0-30% EtOAc/hexanes+2% AcOH)
Quellen und Nachweise
- ORD-Eintrag
- ord-3b969af328634b3ba330d01803a61fe6
- Quelldatensatz
- uspto-grants-2016_08
- Patentnummer
- US09409892B2
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