反应详情

A solution of 22.5 g (0.0318 mole) 4-amino-1-hydroxy-N,N-dioctadecyl-2-naphthamide and 4.0 g (0.5 mole) pyridine in 300 ml tetrahydrofuran (THF) under nitrogen was stirred at room temperature and a solution of 9.0 g (0.036 mole) 2,3-dichloropyridine-5-sulfonyl chloride in 50 ml THF was added. The mixture was stirred 2 hours at room temperature. A thin-layer Chromogram on silica gel sheets indicated unreacted amine, so an additional 1.0 g of the sulfonyl chloride was added followed by 0.5 ml pyridine and stirring for an additional hour. Since a thin-layer chromatogram indicated no more amine, the mixture was concentrated to a small volume on a rotary evaporator, slurried in water several times with the water layer decanted off each time. The oil was dissolved in ether, water was separated, and the extract was dried with anhydrous Na2SO4. The ether layer was removed to leave a reddish oil which solidified on standing. The oil was extracted several times with boiling acetonitrile to leave a purplish black residue. The extracts were chilled and the precipitate was reextracted; chilling the extracts gave 25.7 g (88 percent) of product as a beige powder with a m.p. 88°-9° C.

1. stirringstirring for an additional hour
2. concentrationthe mixture was concentrated to a small volume on a rotary evaporator
3. customdecanted off each time
4. dissolutionThe oil was dissolved in ether
5. customwater was separated
6. dry with materialthe extract was dried with anhydrous Na2SO4
7. customThe ether layer was removed
8. customto leave a reddish oil which
9. extractionThe oil was extracted several times with boiling acetonitrile
10. customto leave a purplish black residue
11. temperatureThe extracts were chilled
12. temperaturechilling the extracts