Réaction #1063

Équation de réaction

acetonitrile

compound ( 8 )

5-(2-bromoacetylamino)-2,3,4,5-tetrahydro-1-benzoxepine

compound ( 4 )

4-(4-phenoxyphenyl)piperidine

→

compound ( 28 )

Rendement 98.0%

5-[2-(4-(4-phenoxyphenyl)piperidin-1-yl)acetylamino]-2,3,4,5-tetrahydro-1-benzoxepine

Rendement 98.0%

Solvants

triethylamine

Conditions de réaction

Traitement

1. 1
   TempératureThis was heated
2. 2
   Températureat reflux for 3 hours
3. 3
   Extractionextraction
4. 4
   AutreThe extract was dried
5. 5
   Filtrationfiltered
6. 6
   Concentrationconcentrated under reduced pressure
7. 7
   Autreto obtain a residue which
8. 8
   Autrewas then purified by silica gel column chromatography (methylene chloride:methanol=25:1)

Mode opératoire

To a 5 ml acetonitrile solution of 190 mg of the compound (8) synthesized in Reference Example 8 were added 184 mg of the compound (4) synthesized in Reference Example 4 and 0.14 ml of triethylamine. This was heated at reflux for 3 hours. To the reaction was added 10 ml of ice water, then extraction was performed with ethyl acetate. The extract was dried, filtered, then concentrated under reduced pressure to obtain a residue which was then purified by silica gel column chromatography (methylene chloride:methanol=25:1) to obtain the above-identified compound (28) in an amount of 300 mg (yield of 98%).

Source