Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641012Generated: October 26, 2026

Tetrahydrofuran → HCID 178462566, compound

https://huagongshe.com/reaction/641012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-(4-Aminophenyl)butanoic acidHCID 27049—
ReactantHCID 178462568HCID 178462568—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 178462566HCID 17846256645%

Reaction Conditions

Temperature65 °C

Reaction Steps

A small screw cap test tube was charged with 4-Chloro-1-ethyl-1H-pyrazole-3-carboxylic acid [3-(3-{[4-(4-methyl-piperazin-1-yl)-phenylamino]-methylene}-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (as prepared in Example 342, 100 mg, 0.229 mmol) and THF (2.5 mL). To the resulting solution was added 4-(4-Amino-phenyl)-butyric acid (41.4 mg, 0.231 mmol), and the mixture was stirred for 24 h at 65° C. Subsequently, the reaction mixture was cooled to room temperature and diluted with EtOAc (5 mL) and Hexane (˜40 mL). The solid that precipitated was collected by filtration and washed with 0° C. acetone (˜10 mL) affording the title compound in 45% yield (0.061 g, 0.102 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07692005B2
Source datasetuspto-grants-2010_04
ORD IDord-7b7a599362b940e1b62d804111c2fb65
Source noteuspto-grants-2010_04