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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977861Generated: November 2, 2026

Triethylamine → N-[(9H-Xanthen-9-yl)methyl]-N'-{2-t-butyl-5-[4-cyclohexyl-3-(t-butyldimethylsilyloxy)butyl]phenyl}urea

https://huagongshe.com/reaction/977861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant2-(9H-xanthen-9-yl)acetic acidHCID 834662—
Reactant2-t-Butyl-5-[4-cyclohexyl-3-(t-butyldimethylsilyloxy)butyl]anilineHCID 19966217—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
ProductN-[(9H-Xanthen-9-yl)methyl]-N'-{2-t-butyl-5-[4-cyclohexyl-3-(t-butyldimethylsilyloxy)butyl]phenyl}ureaHCID 1996606065%

Reaction Steps

A solution of 240 mg (1.00 mmol) of 2-(9H-xanthen-9-yl)acetic acid, 275 mg (1.00 mmol) of diphenylphosphoryl azide and 139 μl (1.00 mmol) of triethylamine in 3 ml of benzene was heated under reflux, with stirring, for 2.5 hours, after which a solution of 459 mg (1.10 mmol) of 2-t-butyl-5-[4-cyclohexyl-3-(t-butyldimethylsilyloxy)butyl]aniline in 0.5 ml of benzene was added. The resulting mixture was heated under reflux for 3 hours. At the end of this time, the reaction mixture was diluted with ethyl acetate, and the diluted mixture was washed with dilute aqueous hydrochloric acid, with water, with a saturated aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, in that order. The organic phase was dried over anhydrous sodium sulfate, and the solvent was removed by distillation under reduced pressure. The resulting residue was purified by column chromatography through 25 g of silica gel, using a 95:5 by volume mixture of methylene chloride and ethyl acetate as the eluent, to give 414 mg (yield 65%) of the title compound as a foam-like material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614550
Source datasetuspto-grants-1997_03
ORD IDord-ea2d9747b10a4588992b0769c43859b4
Source noteuspto-grants-1997_03