Réaction #417967

ord-b7ec9259fc1742a1a147474dad6ba6dd

Équation de réaction

CC(=O)Nc1ccc(Cl)c(O)c1
17a
CC(=O)Nc1ccc(Cl)c(O)c1
N-(4-chloro-3-hydroxyphenyl)acetamide
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
Cl.ClCCN1CCOCC1
4-(2-chloroethyl) morpholine hydrochloride
CC(=O)Nc1ccc(Cl)c(OCCN2CCOCC2)c1
compound 23a
Rendement 69.0%
CC(=O)Nc1ccc(Cl)c(OCCN2CCOCC2)c1
N-[4-chloro-3-(2-morpholin-4-yl-ethoxy)-phenyl]-acetamide
Rendement 69.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

The compound 23a was prepared by using the general procedure H, as given in Example 9, in 69% yield starting from 17a, with 2.5 eq of cesium carbonate and 1.1 eq of 4-(2-chloroethyl) morpholine hydrochloride.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08877752B2uspto-grants-2014_11