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HRID 326183作成日:2026年10月25日

Pyridine 4-methylbenzene-1-sulfonate → (5Z,13E)-(8R,9S,11R,12R,15S,16RS)-9-Chloro-11,15-dihydroxy-16,19-dimethyl-5,13,18-prostatrienoic Acid

https://huagongshe.com/reaction/326183

反応式

関与物質

役割名称HCID仕込み量
反応物Pyridine 4-methylbenzene-1-sulfonateHCID 161440—
反応物(5Z,13E)-(8R,9S,11R,-12R,15S,16RS)-9-chloro-11,15-bis(tetrahydropyran-2-yloxy)-16,19-dimethyl-5,13,18-prostatrienoic acidHCID 67859606—
溶媒EthanolHCID 702—
溶媒DichloromethaneHCID 6344—
生成物(5Z,13E)-(8R,9S,11R,12R,15S,16RS)-9-Chloro-11,15-dihydroxy-16,19-dimethyl-5,13,18-prostatrienoic AcidHCID 6785958842%

反応手順

A solution of 144 mg of (5Z,13E)-(8R,9S,11R,12R,15S,16RS)-9-chloro-11,15-bis(tetrahydropyran-2-yloxy)-16,19-dimethyl-5,13,18-prostatrienoic acid in 2 ml of absolute ethanol was combined with 6.4 mg of pyridine p-toluenesulfonate and agitated for 5 days at room temperature under argon. The reaction mixture was then diluted with 100 ml of methylene chloride, washed twice with saturated sodium chloride solution, dried over magnesium sulfate, and evaporated to dryness under vacuum. The residue was purified by column chromatography on silica gel with hexane/50-100% ethyl acetate as the eluent, thus obtaining 42.5 mg of the desired carboxylic acid as a highly viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04444788
出典データセットuspto-grants-1984_04
ORD IDord-c98d9cf42f884f8caf14e63d9f3ac74f
出典メモuspto-grants-1984_04