Reaktion #45522

ord-5daccee6f7804a778a610f894b45d86c

Reaktionsgleichung

CCOC(=O)/C=C(/CCNC(=O)OCc1ccccc1)N1CCCC1
ethyl (Z)-5-{[(benzyloxy)carbonyl]amino}-3-tetrahydro-1H-1-pyrrolyl-2-pentenoate
[Cl-]
chloride
Cc1noc2cc[nH]c(=O)c12
3-methyl-4,5-dihydroisoxazolo[4,5-c]pyridin-4-one
O=c1[nH]ccc2onc(-c3ccc(Oc4ccccc4)cc3)c12
title compound
O=c1[nH]ccc2onc(-c3ccc(Oc4ccccc4)cc3)c12
3-(4-phenoxyphenyl)isoxazolo[4,5-c]pyridin-4(5H)-one

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeprepared

Vorschrift

The title compound was prepared from 4-phenoxybenzohydroxyiminoyl chloride, prepared using the procedure described in Jones, Raymond C. F. et al, J. Med. Chem. 2003, 46, 87-96, and ethyl (Z)-5-{[(benzyloxy)carbonyl]amino}-3-tetrahydro-1H-1-pyrrolyl-2-pentenoate, prepared using the procedure described in Natale, Nicholas, R. et al, J. Chem. Soc. Perkins Trans. I, 1999, 765-776, using a manner similar to that described in Natale, Nicholas, R. et al, J. Chem. Soc. Perkins Trans. I, 1999, 765-776 for the preparation of 3-methyl-4,5-dihydroisoxazolo[4,5-c]pyridin-4-one. 1H NMR (DMSO-d6, 400 MHz) δ8.31 (d, 2H), 7.66 (d, 1H), 7.46 (t, 2H), 7.22 (t, 1H), 7.1-7.15 (m, 5H), 6.82 (d, 1H); Rt=3.03 min (Conditions a), MS m/e: 303 (M−H)−.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07737160B2uspto-grants-2010_06