Reaktion #85892

ord-748e2ead300e489bbc91e6741afdf325

Reaktionsgleichung

CC(C)(C)OC(=O)N1CC(CNc2nc(Cl)cc3nccnc23)CC(F)(F)C1
tert-butyl 5-((7-chloropyrido[4,3-b]pyrazin-5-ylamino)methyl)-3,3-difluoropiperidine-1-carboxylate
OB(O)c1ccc(N2CCOCC2)cc1
4-morpholinophenylboronic acid
C1CCC(P(C2CCCCC2)C2CCCCC2)CC1
tri(cyclohexyl)phosphine
O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
CC(C)(C)OC(=O)N1CC(CNc2nc(-c3ccc(N4CCOCC4)cc3)cc3nccnc23)CC(F)(F)C1
title compound
CC(C)(C)OC(=O)N1CC(CNc2nc(-c3ccc(N4CCOCC4)cc3)cc3nccnc23)CC(F)(F)C1
tert-butyl 3,3-difluoro-5-((7-(4-morpholinophenyl)pyrido[4,3-b]pyrazin-5-ylamino)methyl)piperidine-1-carboxylate

Lösungsmittel

Reaktionsbedingungen

Temperatur
160°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas sealed in a microwave reaction tube
  2. 2
    TemperaturThe mixture was cooled to room temperature
  3. 3
    Einengenconcentrated under reduced pressure
  4. 4
    Sonstigethe residue was purified by chromatography

Vorschrift

A mixture of tert-butyl 5-((7-chloropyrido[4,3-b]pyrazin-5-ylamino)methyl)-3,3-difluoropiperidine-1-carboxylate (206 mg, 0.5 mmol), 4-morpholinophenylboronic acid (207 mg, 1.0 mmol), tri(cyclohexyl)phosphine (56 mg, 0.2 mmol), Pd2(dba)3 (91 mg, 0.1 mmol) and Cs2CO3 (325 mg, 2.0 mmol) in dimethoxyethane/H2O was sealed in a microwave reaction tube and stirred at 160° C. for 80 minutes in a microwave reactor. The mixture was cooled to room temperature, concentrated under reduced pressure, and the residue was purified by chromatography to give the title compound. MS (m/z): 541 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09434726B2uspto-grants-2016_09