Reaktion #159988

ord-f5e3b4d898c04fed87046d3ce1e0178b

Reaktionsgleichung

CC(C)(C)OC(=O)N1CCc2nc(N3CCS(=O)(=O)CC3)nc(OS(=O)(=O)C(F)(F)F)c2CC1
2-(1,1-dioxo-1λ6-thiomorpholin-4-yl)-4 trifluoromethanesulfonyloxy-5,6,8,9-tetrahydro-pyrimido[4,5-d]azepine-7-carboxylic acid tert-butyl ester
Cc1ccc(B(O)O)cc1
(4-methylphenyl)-boronic acid
O=C([O-])[O-].[K+].[K+]
K2CO3
Cc1ccc(-c2nc(N3CCS(=O)(=O)CC3)nc3c2CCNCC3)cc1
title compound
Ausbeute 64.0%
Cc1ccc(-c2nc(N3CCS(=O)(=O)CC3)nc3c2CCNCC3)cc1
2-(1,1-Dioxo-1λ6-thiomorpholin-4-yl)-4-p-tolyl-6,7,8,9-tetrahydro-5H-pyrimido[4,5-d]azepine
Ausbeute 64.0%

Reaktionsbedingungen

Temperatur
130°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe separated organic layer was filtered over silica gel
  2. 2
    Einengenthe filtrate was concentrated
  3. 3
    SonstigeThe residue was purified by FCC (petroleum ether/Et2O)
  4. 4
    SonstigeThe product fractions were collected
  5. 5
    Sonstigethe solvent was evaporated
  6. 6
    workup.DISSOLUTIONThis residue was dissolved in TFA/DCM/water (5:12:1, 12 mL)
  7. 7
    workup.STIRRINGstirred at rt for 90 min
  8. 8
    EinengenThe mixture was concentrated
  9. 9
    workup.ADDITIONresidue was diluted with 1 M NaOH
  10. 10
    Extraktionextracted with DCM (2×)
  11. 11
    WaschenThe combined organic layers were washed with satd
  12. 12
    TrocknenNaCl, dried
  13. 13
    Einengenconcentrated
  14. 14
    SonstigeThe residue was recrystallized from 2-propanol

Vorschrift

A mixture of 2-(1,1-dioxo-1λ6-thiomorpholin-4-yl)-4 trifluoromethanesulfonyloxy-5,6,8,9-tetrahydro-pyrimido[4,5-d]azepine-7-carboxylic acid tert-butyl ester (0.0008 mol), (4-methylphenyl)-boronic acid (0.0008 mol), Pd(dppf)Cl2 (0.00008 mol) and K2CO3 (0.0016 mol) in 2-propanone/toluene/water (4:4:1, 8 mL) was stirred in a microwave for 30 min at 130° C. The separated organic layer was filtered over silica gel and the filtrate was concentrated. The residue was purified by FCC (petroleum ether/Et2O). The product fractions were collected and the solvent was evaporated. This residue was dissolved in TFA/DCM/water (5:12:1, 12 mL) and stirred at rt for 90 min. The mixture was concentrated and residue was diluted with 1 M NaOH and extracted with DCM (2×). The combined organic layers were washed with satd. NaCl, dried, and concentrated. The residue was recrystallized from 2-propanol to give 0.190 g (64%) of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08829011B2uspto-grants-2014_09