Реакция #345473

Уравнение реакции

water

isopropanol

sodium hydride

N,N-dimethylformamide

2-chloro-9-[4-(bromoacetamido)piperidinomethyl]methanoanthracene

→

title compound

Выход 48.0%

N-(1-[2-Chloro-9,10-dihydro-9,10-methanoanthracen-9-ylmethyl]-4-piperidyl)-2-(isopropoxy)acetamide

Выход 48.0%

Растворители

methylene chloride

Условия реакции

Обработка

1. 1
   ТемператураTo a cooled (ice bath)
2. 2
   workup.STIRRINGAfter stirring for 0.5 h at 0° C.
3. 3
   workup.STIRRINGstirred for an additional 18 h
4. 4
   Фильтрацияfiltered through celite with methylene chloride (3×50 mL) washes
5. 5
   ДругоеAfter separating the aqueous layer from the filtrate
6. 6
   Промывкаthe organic layer was washed with brine (50 mL)
7. 7
   Сушкаdried (sodium sulfate)
8. 8
   Фильтрацияfiltered
9. 9
   Концентрированиеconcentrated
10. 10
    Другоеto give a yellow syrup

Методика

To a cooled (ice bath) stirred suspension of 97% sodium hydride (180 mg, 7.5 mmol) in N,N-dimethylformamide (3 mL) was added isopropanol (0.58 mL, 7.5 mmol). After stirring for 0.5 h at 0° C., the reaction was added 2-chloro-9-[4-(bromoacetamido)piperidinomethyl]methanoanthracene (575 mg, 1.25 mmol) and silver tetrafluoroborate (243 mg, 1.25 mmol). The reaction was allowed to warm to ambient temperature and stirred for an additional 18 h. The mixture was treated with water (50 mL) and methylene chloride (100 mL) and filtered through celite with methylene chloride (3×50 mL) washes. After separating the aqueous layer from the filtrate, the organic layer was washed with brine (50 mL), dried (sodium sulfate), filtered, and concentrated to give a yellow syrup. Chromatography of this material over silica gel (eluant: 9:1 methylene chloride/ether) gave the title compound as a light yellow glass (265 mg, 48%), mp 50.0°-3.0° C.; MS(CI): 439 (M+H); NMR (300 MHz,DMSO-d6): 1.10(d, 6H, J=6.0 Hz), 1.51-1.61(br m, 4H), 2.26(br m, 2H), 2.47(m, 2H), 2.93(br m, 2H), 3.29(d, part.submerged by H2O, 1H), 3.38(d, 1H, J=14.1 Hz), 3.57(septet, 1H, J=6.2 Hz), 3.62(br m, 1H), 3.78(s, 1H), 4.34(s, 1H), 6.96(br m, 3H), 7.20(br d, 2H, J=8.9 Hz), 7.27(d, 2H, J=7.7 Hz), 7.34(d, 1H, J=8.0 Hz).

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