Methyl 2-t-butoxycarbonylamino-4-[4-[4-(4-pyridyl)-piperazin-1-yl]phenoxy]butyrat → Methyl 2-amino-4-[4-[4-(4-pyridyl)piperazin-1-yl]-phenoxy]butyrate

HRID 2249Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2249
C(OC([NH:8][CH:9]([CH2:14][CH2:15][O:16][C:17]1[CH:22]=[CH:21][C:20]([N:23]2[CH2:28][CH2:27][N:26]([C:29]3[CH:34]=[CH:33][N:32]=[CH:31][CH:30]=3)[CH2:25][CH2:24]2)=[CH:19][CH:18]=1)[C:10]([O:12][CH3:13])=[O:11])=O)(C)(C)C>C(O)(C(F)(F)F)=O>[NH2:8][CH:9]([CH2:14][CH2:15][O:16][C:17]1[CH:18]=[CH:19][C:20]([N:23]2[CH2:24][CH2:25][N:26]([C:29]3[CH:34]=[CH:33][N:32]=[CH:31][CH:30]=3)[CH2:27][CH2:28]2)=[CH:21][CH:22]=1)[C:10]([O:12][CH3:13])=[O:11]

Komponenten

3

Edukt 1

HCID 18918622Methyl 2-t-butoxycarbonylamino-4-[4-[4-(4-pyridyl)-piperazin-1-yl]phenoxy]butyrat

Produkt 1

HCID 18918214Methyl 2-amino-4-[4-[4-(4-pyridyl)piperazin-1-yl]-phenoxy]butyrateAusbeute 74,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6422Trifluoroacetic acidLösungsmittel

Versuchsvorschrift

The compound of Example 140 (0.96 g) in TFA (10 ml) was kept at room temperature for 2 hours. The solution was evaporated and the residue dissolved in water (15 ml) and the solution basified with sodium carbonate. The mixture was extracted three times with dichloromethane. Evaporation of the combined extracts gave the title compound (0.56 g); m.p. 125°-127° C.; NMR(d6DMSO) δ 8.2(2H,d), 6.92(6H,m), 4.0(2H,m), 3.64(3H,s), 3.46(4H,t), 3.15(4H,t), 2.04(2H,m), 1.84(1H, m); m/e 371(M+H)+. Calculated for C20H26N4 O3. 0.75 H2O: C, 62.5; H, 7.17; N, 14.6. Found: C, 62.8; H, 6.8; N, 14.3%.

Aufarbeitung

  1. customThe solution was evaporated
  2. dissolutionthe residue dissolved in water (15 ml)
  3. extractionThe mixture was extracted three times with dichloromethane
  4. customEvaporation of the combined extracts

Quellen und Nachweise

ORD-Eintrag
ord-bc4c5bfd0a2540ebba7d4dbbdd3411b3
Quelldatensatz
uspto-grants-1998_03
Patentnummer
US05728701

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