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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383334Generated: October 31, 2026

Tetrahydrofuran → 4-(4-Methylpiperazin-1yl)indole-2-carboxylic acid

https://huagongshe.com/reaction/1383334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant1-(2-(ethoxycarbonyl)-1H-indol-4-yl)-4-methylpiperazineHCID 15550245—
SolventWaterHCID 962—
Product4-(4-Methylpiperazin-1yl)indole-2-carboxylic acidHCID 2118759049%

Reaction Steps

A solution of 1-(2-(ethoxycarbonyl)-1H-indol-4-yl)-4-methylpiperazine (0.91 g, 3.17 mmol), lithium hydroxide hydrate (0.136 g, 3.17 mmol, 1.0 equivalent), tetrahydrofuran (20 mL), and water (4 mL) was heated at reflux under nitrogen for 16 hours. The resulting reaction mixture was evaporated under reduced pressure, and the residue was chromatographed using silica gel (approximately 30 g) and elution with methylene chloride/methanol/ammonium hydroxide [3:2:0.2] to afford the title compound (0.40 g, 1.54 mmol, 49%) as a white solid: mp, 272-273° C.; R, =0.05 in methylene chloride/methanol/ammonium hydroxide [5:1:0.1]; 13C NMR (D2O) δ169.4, 145.0, 137.5, 132.9, 124.7, 120.7, 108.2, 107.3, 103.7, 58.7, 53.7, 51.0; LRMS (m/z, relative intensity) 260 (18), 259 (M+, 100), 244 (9), 215 (7), 170 (24); HRMS calculated for C14H17N3O2 259.1322, found 259.1325.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255306B1
Source datasetuspto-grants-2001_07
ORD IDord-e5ceba4b334244c2ab903fb48b9be35a
Source noteuspto-grants-2001_07