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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635926Generated: October 31, 2026

Tetrahydrofuran → HCID 86758813, compound

https://huagongshe.com/reaction/1635926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant(2-Nitrophenyl)acetic acidHCID 77337—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant5-(4-Fluorophenyl)-4-(4-pyridinyl)-1H-pyrazol-3-amineHCID 15513101—
ProductHCID 86758813HCID 8675881314%

Reaction Steps

Under a stream of argon gas, 543 mg of 2-nitrophenylacetic acid and 486 mg of carbonyldiimidazole were dissolved in 10 ml of tetrahydrofuran, followed by stirring at room temperature for 10 minutes. Then, 254 mg of 3-amino-5-(4-fluorophenyl)-4-(4-pyridyl)pyrazole and 457 mg of DBU were added thereto, followed by stirring at room temperature overnight. After the reaction mixture was concentrated under reduced pressure, the resulting residue was suspended in chloroform, washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and then concentrated. The resulting residue was purified by column chromatography using 40 g of silica gel [with an elution solvent comprising chloroform-methanol (100:1)]. Thus, 70 mg (14% yield) of the title compound was obtained as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06511997B1
Source datasetuspto-grants-2003_01
ORD IDord-cc06a8f82a774264a211d7527115512d
Source noteuspto-grants-2003_01