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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283797Generated: October 31, 2026

Pyridine → HCID 66958558, compound

https://huagongshe.com/reaction/2283797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66958552HCID 66958552—
SolventDichloromethaneHCID 6344—
ProductHCID 66958558HCID 66958558—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 5-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]-1-propyl-1H-pyrazole-3-carboxamide (16.3 g, 50.0 mmol) and pyridine (20.9 mL, 150 mmol) in dichloromethane (100 mL) at 0° C. was added a solution of trifluoroacetic anhydride (9.89 mL, 70.0 mmol) in dichloromethane (100 mL) over ten minutes. The solution was stirred at 0° C. for about 15 minutes, then was allowed to warm to ambient temperature. After 45 minutes, saturated aqueous sodium bicarbonate (200 mL) was added and the dichloromethane was removed under reduced pressure. A white solid was isolated by filtration, washed with water, and dried. The solid was recrystallized from 1:1 heptane/ethyl acetate to yield 5-[2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethyl]-1-propyl-1H-pyrazole-3-carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145410B2
Source datasetuspto-grants-2015_09
ORD IDord-454cd4abb8e34d6e8728c63f993f7bab
Source noteuspto-grants-2015_09