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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338952Generated: October 29, 2026

tert-butyl (S)-1-((R)-2,2,2-trifluoro-1-(6-hydrazinylpyridin-3-yl)ethyl)pyrrolidin-3-ylcarbamate → tert-butyl N-[(3S)-1-[(1R)-2,2,2-trifluoro-1-[6-[(2E)-2-[(7-methoxy-6-methylquinolin-2-yl)methylidene]hydrazinyl]-3-pyridinyl]ethyl]pyrrolidin-3-yl]carbamate

https://huagongshe.com/reaction/338952

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (S)-1-((R)-2,2,2-trifluoro-1-(6-hydrazinylpyridin-3-yl)ethyl)pyrrolidin-3-ylcarbamateHCID 86707414—
Reactant7-Methoxy-6-methylquinoline-2-carbaldehydeHCID 86707472—
SolventEthanolHCID 702—
Producttert-butyl N-[(3S)-1-[(1R)-2,2,2-trifluoro-1-[6-[(2E)-2-[(7-methoxy-6-methylquinolin-2-yl)methylidene]hydrazinyl]-3-pyridinyl]ethyl]pyrrolidin-3-yl]carbamateHCID 140629011—

Reaction Steps

tert-butyl (S)-1-((R)-2,2,2-trifluoro-1-(6-hydrazinylpyridin-3-yl)ethyl)pyrrolidin-3-ylcarbamate (187 mg, 0.497 mmol) and 7-methoxy-6-methylquinoline-2-carbaldehyde (100 mg, 0.497 mmol) in ethanol (5 mL) were stirred at ambient temperature for 24 hours. After concentration, the residue was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-cbb0cbbf5ebf4a71816e614ea14f36d6
Source noteuspto-grants-2014_11