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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273858Generated: November 3, 2026

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

https://huagongshe.com/reaction/273858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamideHCID 20094348—
SolventDichloromethaneHCID 6344—
Product1-acetyl-5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamideHCID 1522520473.6%

Reaction Steps

To a solution of 5-[2-[N-tert-butoxycarbonyl-2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamide (50 mg) in dry methylene chloride (1 ml) were added triethylamine (21 mg) and acetic anhydride (21 mg), and the mixture was stirred at room temperature for 3.5 hours. To the reaction mixture was added water, and the mixture was extracted with methylene chloride. The extract was washed with water and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give 40 mg of 1-acetyl-5-[2-[N-tert-butoxycarbonyl- 2-(2-ethoxyphenoxy)ethylamino]propyl]indoline-7-carboxamide as an amorphous powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387603
Source datasetuspto-grants-1995_02
ORD IDord-b6d001e2b73b4d1a827928f77121cfce
Source noteuspto-grants-1995_02