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HRID 523622作成日:2026年10月26日

Dexamethasone → 2-(2-(2-((8S,9R,10S,11S,16R,17R)-9-fluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[alpha]phenanthren-17-yl)-2-oxoethoxy)-2-oxoethylsulfinyl)ethyl methacrylate methacrylate

https://huagongshe.com/reaction/523622

反応式

関与物質

役割名称HCID仕込み量
反応物DexamethasoneHCID 5743—
反応物Ethyl AcetateHCID 8857—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物2-(2-(Methacryloyloxy)ethylsulfinyl)acetic acidHCID 87170052—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒TetrahydrofuranHCID 8028—
生成物2-(2-(2-((8S,9R,10S,11S,16R,17R)-9-fluoro-11,17-dihydroxy-10,13,16-trimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[alpha]phenanthren-17-yl)-2-oxoethoxy)-2-oxoethylsulfinyl)ethyl methacrylate methacrylateHCID 13173557273%

反応手順

5 (0.54 g, 2.4 mmol, 1.05 eqv.) was dissolved in dry THF (5 mL) and DMAP (0.14 g, 1.2 mmol, 0.5 eqv.) was added to the solution under nitrogen. After cooling on ice, a dexamethasone solution (0.91 g, 2.3 mmol, 1 eqv.) in dry THF (25 mL) and DCC (0.525 g, 2.5 mmol, 1.1 eqv.) were added to the mixture. The reaction mixture was slowly warmed to room temperature and stirred overnight at RT. The completion of the reaction was confirmed by TLC (EtOAc/Hex, 20:1 (v/v), Rf: 0.24). Most of the solvent was evaporated and the remaining solution was purified on a 20 cm silica gel column (EtOAc/Hex, 20:1 (v/v)). 1 g (73% yield) DMSL2 was obtained as a yellow fluffy solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09339554B2
出典データセットuspto-grants-2016_05
ORD IDord-2104005dace845429e12138a9e8602c3
出典メモuspto-grants-2016_05