Sodium hydride → 4-(4-Chlorophenylsulfonylamino)pyrrolidine

To a solution of (4-carboxy-4-methylpentyl)triphenylphosphonium bromide (3.83 g) in dimethyl sulfoxide (21 ml) was added sodium methylsulfinylmethide [19.5 m mol, prepared from sodium hydride (468 mg) and dimethyl sulfoxide (17 ml)]and the solution was stirred at room temperature for 30 minutes. To the resulting solution was added (2S,4R)-1-t-butoxycarbonyl-4-(4-chlorophenylsulfonylamino)-2-formylpyrrolidine (1.0 g) in dimethyl sulfoxide (3.0 ml) and the mixture was stirred at room temperature for 1 hour. After addition of water (50 ml), the solution was washed with ethyl acetate and the aqueous layer was adjusted to pH 1 with 1N hydrochloric acid. The aqueous solution was extracted with ethyl acetate and the organic phase was washed successively with water and brine. The solution was dried over magnesium sulfate and the solvent was evaporated in vacuo to give (2S,4R)-1-t-butoxycarbonyl-2-[(E and Z)-5-carboxy-5-methyl-1-hexenyl]-4-(4-chlorophenylsulfonylamino)pyrrolidine as an oil.

1. stirringthe mixture was stirred at room temperature for 1 hour
2. washthe solution was washed with ethyl acetate
3. extractionThe aqueous solution was extracted with ethyl acetate
4. washthe organic phase was washed successively with water and brine
5. dry with materialThe solution was dried over magnesium sulfate
6. customthe solvent was evaporated in vacuo

ORDレコード

ord-221c7f04ce9e43ffb8ab60ef971428d6

出典データセット

uspto-grants-1990_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US04916152