Dicyclohexylcarbodiimide → (4R,6R)-6-{2-[(1S,2S,6S,8S,8aR)-1,2,6,7,8,8a-Hexahydro-6-t-butyldimethylsilyloxy-8-(3,3-dimethylbutyryloxy)-2-methyl-1-naphthyl]ethyl}tetrahydro-4-t-butyldimethylsilyloxy-2H-pyran-2-one

0.46 ml (3.6 mmol) of 3,3-dimethylbutyric acid, 741 mg (3.6 mmol) of dicyclohexyl carbodiimide and 13 mg (0.09 mmol) of 4-(1-pyrrolidinyl)pyridine were added to a solution of 1.00 g (1.8 mmol) of (4R,6R)-6-{2-[(1S,2S,6S,8S,8aR)-1,2,6,7,8,8a-hexahydro-6-t-butyldimethylsilyloxy-8-hydroxy-2-methyl-1-naphthyl]ethyl}tetrahydro-4-t-butyldimethylsilyloxy-2H-pyran-2-one [prepared as described in Example B, above] in 15 ml of methylene chloride, whilst ice-cooling. The resulting mixture was stirred at the same temperature for 30 minutes and then stirred at room temperature for a further 19 hours. At the end of this time, the solvent was removed by distillation under reduced pressure and the resulting residue was mixed with 20 ml of diethyl ether. Any insoluble material was removed by filtration and then washed twice with diethyl ether, using 5 ml for each washing. The filtrate and the washings were then combined and the solvent was removed by distillation under reduced pressure. The resulting residue was purified by flash column chromatography through silica gel, using a 4:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 555 mg (47% yield) of the title compound.

1. customprepared
2. stirringstirred at room temperature for a further 19 hours
3. customAt the end of this time, the solvent was removed by distillation under reduced pressure
4. additionthe resulting residue was mixed with 20 ml of diethyl ether
5. customAny insoluble material was removed by filtration
6. washwashed twice with diethyl ether
7. customthe solvent was removed by distillation under reduced pressure
8. customThe resulting residue was purified by flash column chromatography through silica gel
9. additionby volume mixture of hexane and ethyl acetate as the eluent

ORDレコード

ord-898fbef8cfc7426686b02ad7530fd3a1

出典データセット

uspto-grants-1998_10

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US05827855