Реакция #1063

Уравнение реакции

acetonitrile

compound ( 8 )

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

compound ( 4 )

4-(4-phenoxyphenyl)piperidine

→

compound ( 28 )

Выход 98.0%

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

Выход 98.0%

Растворители

triethylamine

Условия реакции

Обработка

1. 1
   ТемператураThis was heated
2. 2
   Температураat reflux for 3 hours
3. 3
   Экстракцияextraction
4. 4
   ДругоеThe extract was dried
5. 5
   Фильтрацияfiltered
6. 6
   Концентрированиеconcentrated under reduced pressure
7. 7
   Другоеto obtain a residue which
8. 8
   Другоеwas then purified by silica gel column chromatography (methylene chloride:methanol=25:1)

Методика

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%).

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