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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159658Generated: November 1, 2026

Pyrrolidine → HCID 59514501, compound

https://huagongshe.com/reaction/1159658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59514514HCID 59514514—
SolventDimethylformamideHCID 6228—
ProductHCID 59514501HCID 5951450195%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of methyl {4,6-dichloro-2-[4-(2-naphthoylamino)benzyl]pyrimidin-5-yl}acetate (0.100 g, 0.21 mmol), pyrrolidine (0.019 mL, 0.23 mmol), and N,N-diisopropylethylamine (0.109 mL, 0.62 mmol) in anhydrous DMF (2 mL) was stirred at 80° C. for 5 hours. After cooling to room temperature, the solvent was evaporated and the remaining residue dissolved in EtOAc. This organic solution was sequentially washed with 1N HCl, water, and brine, dried over anhydrous MgSO4, filtered, and concentrated in vacuo. Purification by preparative TLC then afforded methyl {4-chloro-2-[4-(2-naphthoylamino)benzyl]-6-pyrrolidin-1-ylpyrimidin-5-yl}-acetate (0.100 g, 95% yield) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812160B2
Source datasetuspto-grants-2010_10
ORD IDord-73bda969de404a629716228c418f3945
Source noteuspto-grants-2010_10