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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273859Generated: November 1, 2026

Phosphate → 5-[5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]-7-carbamoylindolin-1-yl]-5-oxopentanoic acid

https://huagongshe.com/reaction/273859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphateHCID 1061—
ReactantGlutaric anhydrideHCID 7940—
Reactant5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamideHCID 20094348—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product5-[5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]-7-carbamoylindolin-1-yl]-5-oxopentanoic acidHCID 2009434385.9%

Reaction Steps

To a solution of 5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamide (145 mg) in pyridine (0.5 ml) were added 4-dimethylaminopyridine (4 mg) and glutaric anhydride (51 mg), and the mixture was stirred at room temperature for 72 hours. The pH of the reaction mixture was adjusted to pH 7 with phosphate buffer solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by medium pressure liquid column chromatography on silica gel using a mixture of chloroform and methanol (9/1) as eluent to give 154 mg of 5-[5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]-7-carbamoylindolin- 1-yl]-5-oxopentanoic acid as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387603
Source datasetuspto-grants-1995_02
ORD IDord-439f562608704768943b474f471d9b53
Source noteuspto-grants-1995_02