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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937720Generated: November 1, 2026

Cholesterol → Cholesterol TREN methylphosphonamidate

https://huagongshe.com/reaction/1937720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCholesterolHCID 5997—
ReactantMethyl phosphonic dichlorideHCID 12671—
ReactantAmmonium HydroxideHCID 14923—
ReactantTris(2-aminoethyl)amineHCID 77731—
ReactantN2,N4-dimethylpyridine-2,4-diamineHCID 54550167—
SolventDichloromethaneHCID 6344—
SolventDichloromethane methanolHCID 21226129—
ProductCholesterol TREN methylphosphonamidateHCID 131723226—

Reaction Steps

Refering to FIG. 6, 4-Dimethylaminopyridine (DMAP) (0.31 g, 2.5 mmol) was added to a solution of methylphosphonic dichloride (0.332 g, 2.5 mmol, 31P NMR s, 43.93 ppm) stirring at room temperature under positive pressure argon gas. The resulting clear, colorless solution was cooled to −70° C. and a solution of cholesterol (0.97 g, 2.5 mmol) in anhydrous dichloromethane (20 ml) was added via syringe with vigorous stirring over a period of one hour. The reaction mixture was allowed to warm to room temperature and was maintained for 18 hours at which time 31P NMR analysis of a small aliquot of the reaction mixture indicated complete reaction (d, 39.08 ppm). Crude (13) was treated with additional DMAP (0.31 g, 2.5 mmol) and the reaction mixture cooled to −70° C. while stirring under positive pressure argon. Tris(2-aminoethyl)amine (TREN) (0.37 ml, 2.5 mmol) in anhydrous dichloromethane (20 ml) was added dropwise via syringe over a period of two hours. The reaction mixture was warmed to room temperature and stirred for an additional 18 hours (reaction complete by 31P NMR). Direct loading onto flash silica followed by a gradient of 10 to 20% MeOH/dichloromethane with 1 to 4% NH4OH gave 0.442 g of (18) as a white foam: (yield,28% over two steps), 31P NMR (d, 32.57 ppm), mass spec. calcd=592.89, found=593.49.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395713B1
Source datasetuspto-grants-2002_05
ORD IDord-2ba341af7e4941129d00bb0965f215eb
Source noteuspto-grants-2002_05