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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273860Generated: November 1, 2026

Water → 1-benzoyl-5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamide

https://huagongshe.com/reaction/273860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamideHCID 20094348—
SolventDichloromethaneHCID 6344—
Product1-benzoyl-5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamideHCID 20094374—

Reaction Steps

To a solution of 5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamide (113 mg) in dry methylene chloride (1 ml) were added triethylamine (42 μl) and benzoyl chloride (26 μl) with stirring under ice cooling, and the mixture was stirred at room temperature for 2.5 hours. To the reaction mixture was added water, 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 by using a mixture of chloroform and methanol (20/1) as eluent to give 108 mg of 1-benzoyl-5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamide as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387603
Source datasetuspto-grants-1995_02
ORD IDord-1c35eecbb23d4b529bb9ca1cae4e925a
Source noteuspto-grants-1995_02