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HRID 625147作成日:2026年10月26日

Bis-Aminoethylglycol → {2-[2-(2-Amino-ethoxy)-ethoxy]-ethyl}-carbamic acid (3S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

https://huagongshe.com/reaction/625147

反応式

関与物質

役割名称HCID仕込み量
反応物Bis-AminoethylglycolHCID 70248—
反応物C28H45ClO2HCID 54236888—
溶媒DichloromethaneHCID 6344—
生成物{2-[2-(2-Amino-ethoxy)-ethoxy]-ethyl}-carbamic acid (3S,8S,9S,10R,13R,14S,17R)-17-((R)-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl esterHCID 67367938—

反応手順

A solution of cholesteryl chloroformate (1 g, 2.23 mmol) in 25 mL dichloromethane was added dropwise under stirring to a solution of 2,2′-(ethylenedioxy)bis-(ethylamine) (495 mg, 3.34 mmol) in 75 mL dichloromethane. The reaction was stirred overnight at room temperature. The reaction was diluted with dichloromethane and extracted with water. The organic extract was dried over anhydrous MgSO4 dihydrate, filtered and evaporated. After purification on amino-modified silica gel (eluent: MeCl2→MeCl2/MeOH=975:25 v/v) the product (615 mg) was obtained as a white, waxy solid. MS (ISP): (M+H) 561.5

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09301990B2
出典データセットuspto-grants-2016_04
ORD IDord-e5566a34280a453092c899a8032a84aa
出典メモuspto-grants-2016_04