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Pyridine → N-{1-Ethyl-3-[2-oxo-2(1-pyrrolidinyl)ethyl]-1H-pyrazol-5-yl}-2,2,2-trifluoroacetamide

HRID 1472543
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1472543
[F:1][C:2]([F:18])([F:17])[C:3]([O:5]C1C(F)=C(F)C(F)=C(F)C=1F)=O.[NH2:19][C:20]1[N:24]([CH2:25][CH3:26])[N:23]=[C:22]([CH2:27][C:28]([OH:30])=O)[CH:21]=1.[N:31]1[CH:36]=[CH:35][CH:34]=[CH:33]C=1.N1CCCC1>CN(C=O)C>[CH2:25]([N:24]1[C:20]([NH:19][C:3](=[O:5])[C:2]([F:1])([F:17])[F:18])=[CH:21][C:22]([CH2:27][C:28](=[O:30])[N:31]2[CH2:33][CH2:34][CH2:35][CH2:36]2)=[N:23]1)[CH3:26]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 1049PyridineHCID 31268PyrrolidineHCID 4327891Pentafluorophenyl TrifluoroacetateHCID 23332107(5-amino-1-ethyl-1H-pyrazol-3-yl)acetic acid

Produkt 1

HCID 59314454N-{1-Ethyl-3-[2-oxo-2(1-pyrrolidinyl)ethyl]-1H-pyrazol-5-yl}-2,2,2-trifluoroacetamideAusbeute 44,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

Pentafluorophenyl trifluoroacetate (497 mg, 1.773 mmol) was added dropwise to a stirred solution of (5-amino-1-ethyl-1H-pyrazol-3-yl) acetic acid (150 mg, 0.887 mmol) and pyridine (0.143 mL, 1.773 mmol) in DMF (3 mL). The reaction mixture was stirred for 15 min and pyrrolidine (0.220 mL, 2.66 mmol) was added. The reaction mixture was stirred at 65° C. for 40 min. The mixture was cooled and quenched with water (5 mL) and extracted with EtOAc (3×). The extract was dried over Na2SO4, filtered and concentrated. The residue was purified using RP-HPLC to give product (125 mg). MS: (M+H)+=318.8. 1H NMR (400 MHz, CHLOROFORM-d) ppm 1.32 (t, J=7.2 Hz, 3H), 1.87-2.06 (m, 4 H), 3.46 (t, J=6.8 Hz, 2H), 3.53 (t, J=6.8 Hz, 2H), 3.66 (s, 2H), 4.07 (q, J=7.2 Hz, 2H), 5.30 (s, 1H).

Aufarbeitung

  1. stirringThe reaction mixture was stirred at 65° C. for 40 min
  2. temperatureThe mixture was cooled
  3. customquenched with water (5 mL)
  4. extractionextracted with EtOAc (3×)
  5. dry with materialThe extract was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue was purified

Quellen und Nachweise

ORD-Eintrag
ord-0091b883ce26491caa6049c18b98384f
Quelldatensatz
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09012479B2

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