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HRID 36497作成日:2026年10月25日

Phosphate → (1R,5S,6S)-2-[(4R)-pyrrolidine-2-thion-4-ylthio]-6-[(1R)-1-t-butyldimethylsilyloxyethyl]-1-methylcarbapen-2-em-3-carboxylic acid isobutyryloxymethyl ester

https://huagongshe.com/reaction/36497

反応式

関与物質

役割名称HCID仕込み量
反応物PhosphateHCID 1061—
反応物TriphenylphosphineHCID 11776—
反応物Diphenyl chlorophosphateHCID 75654—
反応物DiisopropylethylamineHCID 81531—
反応物(4S)-4-mercaptopyrrolidin-2-thioneHCID 11051701—
反応物Potassium tert-butoxideHCID 23665647—
反応物isobutyryloxymethyl (5R,6S,7S)-7-[(R)-1-tert-butyldimethylsilyloxymethyl]-5-methyl-4,8-dioxo-1-aza-3-thia-bicyclo-[4.2.0]octan-2-carboxylateHCID 131718995—
溶媒TolueneHCID 1140—
溶媒AcetonitrileHCID 6342—
生成物(1R,5S,6S)-2-[(4R)-pyrrolidine-2-thion-4-ylthio]-6-[(1R)-1-t-butyldimethylsilyloxyethyl]-1-methylcarbapen-2-em-3-carboxylic acid isobutyryloxymethyl esterHCID 1110366542.2%

反応条件

温度-40 °C

反応手順

In 10 ml of toluene were dissolved 500 mg of isobutyryloxymethyl (5R,6S,7S)-7-[(R)-1-tert-butyldimethylsilyloxymethyl]-5-methyl-4,8-dioxo-1-aza-3-thia-bicyclo-[4.2.0]octan-2-carboxylate and 277 mg of triphenylphosphine, 130 mg of potassium tert-butoxide was added thereto under nitrogen gas at -40° C. while stirring, and the mixture was stirred at the same temperature for 50 minutes. To the reaction mixture was added dropwise 10 ml of acetonitrile solution containing 312 mg of diphenyl chlorophosphate at -40° C., and the mixture was stirred for 40 minutes. To the reaction mixture were added 155 mg of (4S)-4-mercaptopyrrolidin-2-thione and 148 mg of diisopropylethylamine, and the mixture was stirred at -20° C. for 80 minutes, and then at -5° C. for 1.5 hours. The reaction mixture was poured into a 0.1M phosphate buffer (pH 7.0) and extracted with ethyl acetate. After the extract was washed and dried, the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (solvent; n-hexane:ethyl acetate:chloroform=5:5:1) to obtain 248 mg of isobutyryloxymethyl (1R,5S,6S)-6-[(R)-1-tert-butyldimethylsilyloxyethyl]-2-[(4R)-pyrrolidin-2-thion-4-ylthio]-1-methylcarbapen-2-em-3-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05414081
出典データセットuspto-grants-1995_05
ORD IDord-aecf9b53f27947c0b6ec1f7fbcb48698
出典メモuspto-grants-1995_05