Diethyl Pyrocarbonate → 2-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-methoxy-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]prop-2-enamide

HRID 1479870

Reaktionsgleichung

Reaktionsgleichung von HRID 1479870
[CH2:1]([N:3]([S:9]([C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=1)(=[O:11])=[O:10])[C:4](=[CH2:8])[C:5]([OH:7])=O)[CH3:2].CCOC(OC(OCC)=O)=O.[CH3:30][O:31][C:32]1[CH:37]=[C:36]([CH2:38][NH2:39])[CH:35]=[C:34]([C:40]2[CH:45]=[CH:44][C:43]([C:46]([F:49])([F:48])[F:47])=[CH:42][CH:41]=2)[N:33]=1>C1COCC1>[CH2:1]([N:3]([S:9]([C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][CH:13]=1)(=[O:11])=[O:10])[C:4](=[CH2:8])[C:5]([NH:39][CH2:38][C:36]1[CH:35]=[C:34]([C:40]2[CH:41]=[CH:42][C:43]([C:46]([F:47])([F:48])[F:49])=[CH:44][CH:45]=2)[N:33]=[C:32]([O:31][CH3:30])[CH:37]=1)=[O:7])[CH3:2]

Komponenten

5

Edukt 3

HCID 3051Diethyl PyrocarbonateHCID 903842012-[Ethyl-(4-fluorophenyl)sulfonyl-amino]prop-2-enoic acidHCID 90390870[2-Methoxy-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamine

Produkt 1

HCID 903902042-[ethyl-(4-fluorophenyl)sulfonyl-amino]-N-[[2-methoxy-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methyl]prop-2-enamideAusbeute 30,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

A solution of acid 4B (0.31 g, 1.1 mmol) in THF (20 mL) was added with DEPC (0.22 mL, 1.3 mol eq) and the mixture was stirred at room temperature several minutes. Then [2-methoxy-6-[4-(trifluoromethyl)phenyl]-4-pyridyl]methanamine 27I (0.36 g, 1.1 mol eq) and a catalytic amount of TEA were added, then the reaction mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure, water was added to the residue that is extracted with EtOAc (3×30 mL) and washed with brine (1×40 mL). The separated organic phase was dried over Na2SO4, evaporated to dryness and the residue was purified by flash chromatography (1/1 EtOAc/Petroleum ether) to afford a white solid (180 mg) after crystallization from ethyl ether. Yield=30%. 1HNMR (DMSO, 200 MHz) δ 1.08 (t, 3H, J=6), 3.39 (m, 2H), 3.95 (s, 3H), 4.45 (d, 2H, J=6.2), 5.14 (s, 1H), 6.13 (s, 1H), 6.79 (s, 1H), 7.47 (t, 2H, J=8.2), 7.64 (s, 1H), 7.85 (m, 4H), 8.31 (d, 2H, J=7.8), 8.84 (bt, 1H). [M+1] 537.05 (C25H23F4N3O4S requires 537.53).

Aufarbeitung

  1. stirringthe reaction mixture was stirred at room temperature overnight
  2. customThe solvent was removed under reduced pressure, water
  3. additionwas added to the residue that
  4. extractionis extracted with EtOAc (3×30 mL)
  5. washwashed with brine (1×40 mL)
  6. dry with materialThe separated organic phase was dried over Na2SO4
  7. customevaporated to dryness
  8. customthe residue was purified by flash chromatography (1/1 EtOAc/Petroleum ether)

Quellen und Nachweise

ORD-Eintrag
ord-eab68d159d5a473a933d14e597d40578
Quelldatensatz
uspto-grants-2016_08
Patentnummer
US09409864B2

Verknüpfte Notizen

Wird geladen…