Reaktion #2298631

ord-0a99f9f82b7e47b9a5a2b51cc9c7ed24

Reaktionsgleichung

CCc1nc(C)cc(=O)[nH]1
2-ethyl-4-methyl-1,6-dihydro-6-pyrimidone
O=Cc1ccc(OCCBr)cc1
4-[2-bromoethoxy]benzaldehyde
[H-].[Na+]
NaH
CCc1nc(C)cc(=O)n1CCOc1ccc(C=O)cc1
title compound
Ausbeute 42.0%
CCc1nc(C)cc(=O)n1CCOc1ccc(C=O)cc1
4-[2-[2-Ethyl-4-methyl-6-oxo-1,6-dihydro-1-pyrimidinyl]ethoxy]benzaldehyde
Ausbeute 42.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

The title compound (1.7 g, 42%) was prepared from 2-ethyl-4-methyl-1,6-dihydro-6-pyrimidone (2.0 g, 14.49 mmol), 4-[2-bromoethoxy]benzaldehyde (332 g, 14.19 mmol). LIBr (2.9 g, 33.33 mmol) and NaH (0.45 g, 18.84 mmol) as base, by a similar procedure to that described in preparation 1.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE039266E1uspto-grants-2006_09