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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960313Generated: October 26, 2026

Tetrahydrofuran → {4-[(2-{7-[methyl(2-thienylsulfonyl)amino]-1H-indol-2-yl)-1,3-thiazol-5-yl)methyl]piperazin-1-yl}acetic acid

https://huagongshe.com/reaction/1960313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
Reactantethyl{4-[(2-{7-[methyl(2-thienylsulfonyl)amino]-1H-indol-2-yl}-1,3-thiazol-5-yl)methyl]piperazin-1-yl)acetateHCID 59303517—
SolventMethanolHCID 887—
Product{4-[(2-{7-[methyl(2-thienylsulfonyl)amino]-1H-indol-2-yl)-1,3-thiazol-5-yl)methyl]piperazin-1-yl}acetic acidHCID 5913561777.3%

Reaction Steps

To a solution of ethyl{4-[(2-{7-[methyl(2-thienylsulfonyl)amino]-1H-indol-2-yl}-1,3-thiazol-5-yl)methyl]piperazin-1-yl}acetate (0.490 g) in a mixed solvent of tetrahydrofuran (10 ml) and methanol (5 ml) was added 8N aqueous sodium hydroxide solution (1.5 ml), and the mixture was stirred at room temperature for 16 hr. Saturated aqueous ammonium chloride solution was added to the reaction solution, and the precipitated crystals were collected by filtration, washed with ethyl acetate and water, and dried to give the title compound (0.360 g, yield 57%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410087B2
Source datasetuspto-grants-2013_04
ORD IDord-f0a465d1768e4ee792c474b3fa28b3f8
Source noteuspto-grants-2013_04