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Potassium tert-butoxide → HCID 178499450, Verbindung

HRID 1852482
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1852482
[C:1]([C:4]1[C:5]([NH:25][C:26]2[CH:31]=[CH:30][C:29]([CH2:32][C:33]([O:35][CH3:36])=[O:34])=[CH:28][CH:27]=2)=[N:6][N:7](C2(CC#N)CCN(C(OC(C)(C)C)=O)CC2)[CH:8]=1)(=[O:3])[NH2:2].CC([O-])(C)C.[K+]>C1COCC1.[NH4+].[Cl-]>[C:1]([C:4]1[C:5]([NH:25][C:26]2[CH:27]=[CH:28][C:29]([CH2:32][C:33]([O:35][CH3:36])=[O:34])=[CH:30][CH:31]=2)=[N:6][NH:7][CH:8]=1)(=[O:3])[NH2:2]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 23665647Potassium tert-butoxideHCID 86729389tert-butyl 4-(4-carbamoyl-3-{[4-(2-methoxy-2-oxoethyl)phenyl]amino}-1H-pyrazol-1-yl)-4-(cyanomethyl)piperidine-1-carboxylate

Produkt 1

HCID 178499450HCID 178499450, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028TetrahydrofuranLösungsmittelHCID 25517Ammonium Chloride
Lösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of tert-Butyl 4-(4-carbamoyl-3-{[4-(2-methoxy-2-oxoethyl)phenyl]amino}-1H-pyrazol-1-yl)-4-(cyanomethyl)piperidine-1-carboxylate (226 mg, 0.46 mmol) in THF (2.3 mL) at 0° C. was added KOtBu (0.68 mL, 0.68 mmol, 1.0M in THF), and the mixture was stirred at 0° C. for 20 minutes, then ambient temperature for 20 minutes. The mixture was diluted with saturated aqueous NH4Cl, and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous MgSO4, and concentrated in vacuo. Et2O (5 mL) was added to the resulting oily residue and a solid precipitated out. This solid was collected by decant, and washed with Et2O to afford the title compound. LRMS (ESI) calc'd for C13H15N4O3 [M+H]+: 275. Found: 275.

Aufarbeitung

  1. waitambient temperature for 20 minutes
  2. extractionextracted with EtOAc
  3. washThe organic layer was washed with brine
  4. dry with materialdried over anhydrous MgSO4
  5. concentrationconcentrated in vacuo
  6. additionEt2O (5 mL) was added to the resulting oily residue
  7. customa solid precipitated out
  8. customThis solid was collected
  9. customby decant
  10. washwashed with Et2O

Quellen und Nachweise

ORD-Eintrag
ord-8ed422a1a7504791a16650a0c06fc589
Quelldatensatz
uspto-grants-2015_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08962608B2

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