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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010885Generated: October 30, 2026

Pyrrolidine → HCID 67313348, compound

https://huagongshe.com/reaction/1010885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86625211HCID 86625211—
SolventDimethylformamideHCID 6228—
ProductHCID 67313348HCID 67313348—

Reaction Steps

20 mg of the compound [3-2] was dissolved in 0.4 mL of N,N-dimethylformamide, and 7 μL of pyrrolidine was added thereto. The reaction mixture was stirred for 30 minutes at room temperature, and then thereto was added a saturated aqueous solution of sodium hydrogen carbonate, and the mixture was extracted with chloroform. The resulting organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The insolubles were filtered, the filtrate was concentrated under reduced pressure, and the resulting residue was purified by preparative thin-layer chromatography, to obtain 3 mg of 4-(8-methylimidazo[1,2-a]pyridin-3-yl)-2-({(1S)-1-[4-(pyrrolidin-1-ylacetyl) phenyl]ethyl}amino)pyrimidine-5-carbonitrile [3-3] (hereinafter, referred to as the compound [3-3]) as a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977336B2
Source datasetuspto-grants-2011_07
ORD IDord-60cd8e9b9b9e48e79df988c1fe8f40dd
Source noteuspto-grants-2011_07