反应 #40378

ord-4ed08f9c2c624361bf82204397ccf5ba

反应方程式

CCOC(O)C(=O)c1cccc2c1OC(OCc1ccccc1)C(=O)N2
benzyloxy-8-(2-ethoxy-2-hydroxyacetyl)-4H-benzo[1,4]oxazin-3-one
Cc1cc(CC(C)(C)N)ccc1F
2-(4-fluoro-3-methylphenyl)-1,1-dimethylethylamine
Cl
hydrochloride
Cc1cc(CC(C)(C)NCC(O)c2cc(OCc3ccccc3)cc3c2OCC(=O)N3)ccc1F
6-benzyloxy-8-{2-[2-(4-fluoro-3-methylphenyl)-1,1-dimethylethylamino]-1-hydroxyethyl}-4H-benzo[1,4]oxazin-3-one

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

1.10 g (3.1 mmol) of benzyloxy-8-(2-ethoxy-2-hydroxyacetyl)-4H-benzo[1,4]oxazin-3-one and 0.50 g (2.8 mmol) of 2-(4-fluoro-3-methylphenyl)-1,1-dimethylethylamine are reacted and worked up analogously to the method for Example 8(d). White solid. Yield: 0.75 g (47%, hydrochloride); melting point 228° C.-230° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07727984B2uspto-grants-2010_06