反应详情

A solution of 2,5-dichloro-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-pyridine-4-carboxamide (0.50 g, Example 1a) and 1-t-butoxycarbonylhomopiperazine (0.76 g) in dimethylsulfoxide (5 ml) was heated at 100-120° C. for 24 hours. The solution was cooled and partitioned between saturated aqueous sodium bicarbonate solution and dichloromethane and the organic layer dried over magnesium sulphate. Concentration in vacuo and chromatography on silica gave a colourless solid. This was redissolved in methanol (10 ml) and treated with 4M HCl in dioxan (2 ml). Once deprotection was complete (14 hours) the solution was partially concentrated in vacuo then diluted slowly with diethyl ether with rapid stirring. The resulting white precipitate was filtered, washed with diethyl ether and dried to afford the title compound (0.51 g).

1. temperatureThe solution was cooled
2. custompartitioned between saturated aqueous sodium bicarbonate solution and dichloromethane
3. dry with materialthe organic layer dried over magnesium sulphate
4. concentrationConcentration in vacuo and chromatography on silica
5. customgave a colourless solid
6. custom(14 hours)
7. concentrationwas partially concentrated in vacuo
8. additionthen diluted slowly with diethyl ether with rapid stirring
9. filtrationThe resulting white precipitate was filtered
10. washwashed with diethyl ether
11. customdried