Reaktion #62158

ord-5e86205749a6458a80277b4e27cc3a64

Reaktionsgleichung

O=C(Cc1ccncc1)c1ccc(OCc2ccc3ccccc3n2)cc1
2-pyridin-4-yl-1-[4-(quinolin-2-ylmethoxy)-phenyl]-ethanone
CON(C)C(=O)c1ccc(OCc2ccc3ccccc3n2)c(Cl)c1
3-Chloro-N-methoxy-N-methyl-4-(quinolin-2-ylmethoxy)-benzamide
→
O=C(Cc1ccncc1)c1ccc(OCc2ccc3ccccc3n2)c(Cl)c1
title compound
O=C(Cc1ccncc1)c1ccc(OCc2ccc3ccccc3n2)c(Cl)c1
1-[3-Chloro-4-(quinolin-2-ylmethoxy)-phenyl]-2-pyridin-4-yl-ethanone

Edukte

O=C(Cc1ccncc1)c1ccc(OCc2ccc3ccccc3n2)cc1
2-pyridin-4-yl-1-[4-(quinolin-2-ylmethoxy)-phenyl]-ethanone
CON(C)C(=O)c1ccc(OCc2ccc3ccccc3n2)c(Cl)c1
3-Chloro-N-methoxy-N-methyl-4-(quinolin-2-ylmethoxy)-benzamide

Reagenzien

Keine

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

Following the procedure for the preparation of 2-pyridin-4-yl-1-[4-(quinolin-2-ylmethoxy)-phenyl]-ethanone but substituting 3-Chloro-N-methoxy-N-methyl-4-(quinolin-2-ylmethoxy)-benzamide provided the title compound. (M+H m/z=389.0).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07429665B2uspto-grants-2008_09