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

HRID 62498
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 62498
[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, 4H), 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-50ec0a766cd94d22991785bd4b462b84
Quelldatensatz
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09446034B2

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