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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641686Generated: November 3, 2026

Ethanolamine → HCID 57736474, compound

https://huagongshe.com/reaction/1641686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant5-[(2,5-Difluorophenyl)[(4-fluorophenyl)sulfonyl]methyl]-4-methylpyridine-2-carboxylic acidHCID 57736439—
SolventDichloromethaneHCID 6344—
ProductHCID 57736474HCID 5773647492%

Reaction Steps

To a solution of 5-[(2,5-difluorophenyl)[(4-fluorophenyl)sulfonyl]methyl]-4-methylpyridine-2-carboxylic acid (421 mg, 1.00 mmol) obtained in Example 12 in methylene chloride (10 ml), 2-aminoethanol (0.067 ml, 1.10 mmol), 1-hydroxybenzotriazole (149 mg, 1.10 mmol) 4-methylmorpholine (0.12 ml, 1.10 mmol), and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (211 mg, 1.10 mmol) were added at room temperature. After stirring for 7 days at room temperature, the reaction mixture was washed with saturated aqueous sodium hydrogencarbonate. The organic layer was dried over anhydrous sodium sulfate and filtered, then the filtrate was concentrated under reduced pressure, and the resulting residue was subjected to flash silica gel chromatography. The fraction obtained from an elution with hexane:ethyl acetate=2:3 was concentrated under reduced pressure, and the resulting residue was washed with a mixed solvent of ethanol and hexane, and was collected by filtration, to obtain the title compound (427 mg, 0.92 mmol, 92%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114886B2
Source datasetuspto-grants-2012_02
ORD IDord-db8b7f68872b447ba14eedd0b428558e
Source noteuspto-grants-2012_02