Hydrochloric Acid → 3-Benzyloxy-4-(1-tert-butoxycarbonylmethyl-2,2-diethyoxy-ethylsulfamoyl-)benzoic acid
Reaktionsgleichung
C[O:2][C:3](=[O:38])[C:4]1[CH:9]=[CH:8][C:7]([S:10](=[O:29])(=[O:28])[NH:11][CH:12]([CH2:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH:13]([O:17][CH2:18][CH3:19])[O:14][CH2:15][CH3:16])=[C:6]([O:30][CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH:5]=1.[OH-].[Li+].Cl>C(OCC)(=O)C>[CH2:31]([O:30][C:6]1[CH:5]=[C:4]([CH:9]=[CH:8][C:7]=1[S:10](=[O:28])(=[O:29])[NH:11][CH:12]([CH2:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH:13]([O:17][CH2:18][CH3:19])[O:14][CH2:15][CH3:16])[C:3]([OH:38])=[O:2])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3-Benzyloxy-4-(1-tert-butoxycarbonylmethyl-2,2-diethoxy-ethylsulfamoyl)-benzoic acid methyl ester (6.82 g, 12.4 mmol) was combined and stirred with 1M lithium hydroxide (26 mL, 26 mmol) in tetrohydrofuran (250 mL) at room temperature overnight. The reaction mixture was diluted with ethyl acetate and acidified with 1M HCl (26 mL). The organic layer was collected and extracted with water, brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to give 3-benzyloxy-4-(1-tert-butoxycarbonylmethyl-2,2-diethyoxy-ethylsulfamoyl-)benzoic acid (4.32 g, 8.0 mmol, 65%). MS (APCI) m/z 536.3 (M−1).
Aufarbeitung
- customThe organic layer was collected
- extractionextracted with water, brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-b2824492aa2a4b70be01d1cda49bc815
- Quelldatensatz
- uspto-grants-2005_04
- Patentnummer
- US06875765B2
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