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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695232Generated: October 25, 2026

Formate → HCID 178520651, compound

https://huagongshe.com/reaction/1695232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormateHCID 283—
ReactantButyric acid, 4-piperidino-HCID 20794—
ReactantHCID 178507318HCID 178507318—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 178520651HCID 17852065145.5%

Reaction Steps

To a suspension of 4-piperidin-1-yl-butyric acid (621.0 mg, 3.0 mmol, 1.5 eq) in 1,2-dichloroethane (6 mL), N,N′-carbonyldiimidazole (453.0 mg, 2.8 mmol, 1.4 eq) was added and the mixture was stirred at room temperature for 1 hour. 5-(1H-indol-3-yl)-2H-pyrazol-3-ylamine (400.0 mg, 2.0 mmol, 1.0 eq) in 1,2-dichloroethane (6 mL) was added; the reaction was stirred at room temperature for 2 days, then 1 day at 70° C., to allow complete migration of the acyl group from the ring nitrogen to the exocyclic nitrogen. The reaction then was allowed to cool down to room temperature and the mixture was washed with saturated Na2CO3 and evaporated under reduced pressure; the crude was purified by preparative HPLC to give 320.0 mg (yield: 41%) of the title compound as formate salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163729B2
Source datasetuspto-grants-2012_04
ORD IDord-b81084ead30742eb84fa98e4418c991d
Source noteuspto-grants-2012_04