Reaktion #159610

ord-a40d6ea9459f469596356e90bc537a2c

Reaktionsgleichung

Cl.OC1CNC1
azetidin-3-ol hydrochloride
CCN(CC)CC
trietylamine
COC(=O)c1cccnc1Cl
methyl 2-chloropyridine-3-carboxylate
COC(=O)c1cc(Cl)cnc1N1CC(O)C1
title compound ( D62 )
COC(=O)c1cc(Cl)cnc1N1CC(O)C1
methyl 5-chloro-2-(3-hydroxyazetidin-1-yl)nicotinate

Lösungsmittel

Reaktionsbedingungen

Temperatur
150°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe residue obtained
  2. 2
    Sonstigeafter solvent evaporation
  3. 3
    Sonstigewas purified by SPE-Si cartridge (10 g)
  4. 4
    Wascheneluting with a mixture cyclohexane/ethylacetate from 90/10 to 60/40
  5. 5
    SonstigeCollected fractions after solvent evaporation

Vorschrift

To a solution of azetidin-3-ol hydrochloride (637 mg, 5.82 mmol, commercially available from Matrix Scientific #011272) and trietylamine (1.69 ml, 12.11 mmol) in methanol (10 ml), methyl 2-chloropyridine-3-carboxylate (1 g, 4.84 mmol) was added and the mixture stirred at 150° C. under microwave irradiation 10 min (2 cycles of 5 min each). The residue obtained after solvent evaporation was purified by SPE-Si cartridge (10 g) eluting with a mixture cyclohexane/ethylacetate from 90/10 to 60/40. Collected fractions after solvent evaporation afforded the title compound (D62) (D004/099/1) (800 mg)

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08828987B2uspto-grants-2014_09