Réaction #417968

ord-d9c152a8d2914cc79373a2b96b41a6d5

Équation de réaction

CC(=O)Nc1ccc(Cl)c(O)c1
17a
CC(=O)Nc1ccc(Cl)c(O)c1
N-(4-chloro-3-hydroxyphenyl)acetamide
CN(C)CCCl.Cl
2-dimethylamino ethyl chloride hydrochloride
→
CC(=O)Nc1ccc(Cl)c(OCCN(C)C)c1
compound 24a
Rendement 80.0%
CC(=O)Nc1ccc(Cl)c(OCCN(C)C)c1
N-[4-chloro-3-(2-dimethylamino-ethoxy)-phenyl]-acetamide
Rendement 80.0%

Réactifs

CC(=O)Nc1ccc(Cl)c(O)c1
17a
CC(=O)Nc1ccc(Cl)c(O)c1
N-(4-chloro-3-hydroxyphenyl)acetamide
CN(C)CCCl.Cl
2-dimethylamino ethyl chloride hydrochloride

Réactifs

Aucun

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

The compound 24a was prepared starting from 17a and 2-dimethylamino ethyl chloride hydrochloride, following the general procedure H, as given in Example 9, in 80% yield.

Source

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