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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625147Generated: October 26, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis-AminoethylglycolHCID 70248—
ReactantC28H45ClO2HCID 54236888—
SolventDichloromethaneHCID 6344—
Product{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—

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09301990B2
Source datasetuspto-grants-2016_04
ORD IDord-e5566a34280a453092c899a8032a84aa
Source noteuspto-grants-2016_04