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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 640879Generated: October 30, 2026

5-Amino-2-methoxyphenol → 5-Acetyl-thiophene-2-carboxylic acid (4-{3-[(3-hydroxy-4-methoxy-phenylamino)-methylene]-2-oxo-2,3-dihydro-1H-indole-6-carbonyl}-phenyl)-amide

https://huagongshe.com/reaction/640879

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-methoxyphenolHCID 74314—
ReactantHCID 178466654HCID 178466654—
SolventTetrahydrofuranHCID 8028—
Product5-Acetyl-thiophene-2-carboxylic acid (4-{3-[(3-hydroxy-4-methoxy-phenylamino)-methylene]-2-oxo-2,3-dihydro-1H-indole-6-carbonyl}-phenyl)-amideHCID 7322448374%

Reaction Conditions

Temperature65 °C

Reaction Steps

A small screw cap test tube was charged with 5-Acetyl-thiophene-2-carboxylic acid [4-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (as prepared in Example 34, 40 mg, 0.093 mmol) and THF (2 mL). To the resulting solution was added 5-amino-2-methoxyphenol (16 mg, 0.115 mmol), and the mixture was stirred for 24 h at 65° C. Subsequently, the reaction mixture was cooled to room temperature and concentrated in vacuo. The solid residue was recrystallized with ˜5 mL of i-prOH affording the title compound in 74% yield (0.038 g, 0.0686 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07692005B2
Source datasetuspto-grants-2010_04
ORD IDord-a22191cc189044c193d23b4f5ab00e09
Source noteuspto-grants-2010_04