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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (S)-(-)-2-Aminomethyl-1-ethylpyrrolidine | HCID 643457 | — |
| Reactant | HCID 68750379 | HCID 68750379 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178472022 | HCID 178472022 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569484B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-5c37cae89df24c88a7544463ded4b3f5 |
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| Source note | uspto-grants-2013_10 |
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