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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338889Generated: October 26, 2026

Acetic acid;iodosylbenzene → tert-butyl (S)-1-((R)-2,2,2-trifluoro-1-(3-(6-fluoro-8-isopropoxyquinolin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)ethyl)pyrrolidin-3-ylcarbamate

https://huagongshe.com/reaction/338889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid;iodosylbenzeneHCID 73357407—
Reactanttert-butyl N-[(3S)-1-[(1R)-2,2,2-trifluoro-1-[6-[(2E)-2-[(6-fluoro-8-propan-2-yloxyquinolin-2-yl)methylidene]hydrazinyl]-3-pyridinyl]ethyl]pyrrolidin-3-yl]carbamateHCID 140628990—
SolventDichloromethaneHCID 6344—
Producttert-butyl (S)-1-((R)-2,2,2-trifluoro-1-(3-(6-fluoro-8-isopropoxyquinolin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)ethyl)pyrrolidin-3-ylcarbamateHCID 8670743379.3%

Reaction Steps

To tert-butyl (S)-1-((R)-2,2,2-trifluoro-1-(6-((E)-2-((6-fluoro-8-isopropoxyquinolin-2-yl)methylene)hydrazinyl)pyridin-3-yl)ethyl)pyrrolidin-3-ylcarbamate (157 mg, 0.266 mmol) in DCM (10 mL) was added iodosobenzene diacetate (94.2 mg, 0.292 mmol) and the reaction was stirred at ambient temperature for 2 hours. The reaction was concentrated to dryness and the residue purified by reverse phase chromatography (SP4, 12M, eluting with a gradient of water/ACN 100:0 to 0:100, 20 column volumes) to yield tert-butyl (S)-1-((R)-2,2,2-trifluoro-1-(3-(6-fluoro-8-isopropoxyquinolin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)ethyl)pyrrolidin-3-ylcarbamate (124 mg, 79.3% yield) as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-b1c6262a242f44009ebd3ca3f70bd52e
Source noteuspto-grants-2014_11