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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047161Generated: October 30, 2026

(S)-(-)-2-Aminomethyl-1-ethylpyrrolidine → HCID 178472022, compound

https://huagongshe.com/reaction/1047161

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(-)-2-Aminomethyl-1-ethylpyrrolidineHCID 643457—
ReactantHCID 68750379HCID 68750379—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178472022HCID 17847202267%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2-(2,6-difluoro-5-iodonicotinoyl)-3-(dimethylamino)acrylate (Intermediate 37, 0.500 g, 1.10 mmol) was taken up THF (40 mL) and cooled to 0° C. for 10 min and then (S)-(1-ethylpyrrolidin-2-yl)methanamine (0.153 mL, 1.10 mmol) was added and stirred at room temperature for 2 min. The reaction mixture was quenched with sat NH4Cl diluted with EtOAc and separated, dried, and solvent removed. The residue was purified by a 0-5% gradient on the ISCO of DCM/Methanol to give (S)-ethyl 2-(2,6-difluoro-5-iodonicotinoyl)-3-((1-ethylpyrrolidin-2-yl)methylamino)acrylate (0.360 g, 67%) as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569484B2
Source datasetuspto-grants-2013_10
ORD IDord-5c37cae89df24c88a7544463ded4b3f5
Source noteuspto-grants-2013_10