Potassium Carbonate → di(tert-butyl) 1-(4-hydroxybutyl)-2-propyl-2H-pyrazolo[3,4-c]quinolin-4-ylimidodicarbonate

HRID 1360480Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1360480
C(=O)([O-])[O-].[K+].[K+].C([O:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]1[N:16]([CH2:43][CH2:44][CH3:45])[N:17]=[C:18]2[C:27]=1[C:26]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[N:20]=[C:19]2[N:28]([C:36]([O:38][C:39]([CH3:42])([CH3:41])[CH3:40])=[O:37])[C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])(=O)C>CO>[OH:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]1[N:16]([CH2:43][CH2:44][CH3:45])[N:17]=[C:18]2[C:27]=1[C:26]1[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=1[N:20]=[C:19]2[N:28]([C:36]([O:38][C:39]([CH3:42])([CH3:41])[CH3:40])=[O:37])[C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30]

Komponenten

4

Versuchsvorschrift

Potassium carbonate (6 mg, 0.041 mmol) was added to a solution of 4-{4-[bis(tert-butoxycarbonyl)amino]-2-propyl-2H-pyrazolo[3,4-c]quinolin-1-yl}butyl acetate (0.8823 g, 1.632 mmol) in methanol (5 mL). The mixture was stirred at ambient temperature for 1.3 hours. The volatiles were removed under reduced pressure. The resulting oil was purified by flash chromatography (silica gel, eluted with 100% ethyl acetate) to yield 0.1466 g of di(tert-butyl) 1-(4-hydroxybutyl)-2-propyl-2H-pyrazolo[3,4-c]quinolin-4-ylimidodicarbonate in about 87% purity.

Aufarbeitung

  1. customThe volatiles were removed under reduced pressure
  2. customThe resulting oil was purified by flash chromatography (silica gel, eluted with 100% ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-af196d72fbb840d991631e51e625ab2d
Quelldatensatz
uspto-grants-2011_02
Patentnummer
US07879849B2

Notizen zur Reaktion

Wird geladen…