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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641033Generated: October 30, 2026

4-(4-Aminophenyl)butanoic acid → 4-[4-[[6-[3-[(3-methylthiophene-2-carbonyl)amino]benzoyl]-2-oxo-1H-indol-3-ylidene]methylamino]phenyl]butanoic acid

https://huagongshe.com/reaction/641033

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Aminophenyl)butanoic acidHCID 27049—
ReactantHCID 178429651HCID 178429651—
SolventTetrahydrofuranHCID 8028—
Product4-[4-[[6-[3-[(3-methylthiophene-2-carbonyl)amino]benzoyl]-2-oxo-1H-indol-3-ylidene]methylamino]phenyl]butanoic acidHCID 17842964943%

Reaction Conditions

Temperature65 °C

Reaction Steps

A small screw cap test tube was charged with 3-Methyl-thiophene-2-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (as prepared in Example 352, 200 mg, 0.4945 mmol) and THF (5.0 mL). To the resulting solution was added 4-(4-Amino-phenyl)-butyric acid (88.6 mg, 0.494 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 crude residue was purified by flash silica gel chromatography (CHCl3:MeOH mix eluant with gradient of 1% MeOH to 15% MeOH) to afford the title compound in 43% yield (0.120 g, 0.212 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07692005B2
Source datasetuspto-grants-2010_04
ORD IDord-88bb3ec3b0f24e1796b19d87697bd6e6
Source noteuspto-grants-2010_04