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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876439Generated: October 29, 2026

Iodo benzene diacetate → 8-(Tert-butyldimethylsilyloxy)-2-(6-fluoro[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinoline

https://huagongshe.com/reaction/876439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodo benzene diacetateHCID 12217721—
Reactant5-Fluoro-2-hydrazinylpyridineHCID 19916786—
Reactant8-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehydeHCID 58567082—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product8-(Tert-butyldimethylsilyloxy)-2-(6-fluoro[1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolineHCID 6723113257%

Reaction Conditions

Temperature0 °C

Reaction Steps

8-(tert-butyldimethylsilyloxy)quinoline-2-carbaldehyde (1.39 g, 4.83 mmol) and 5-fluoro-2-hydrazinylpyridine (1.28 g, 6.04 mmol) were combined in DCM (12.1 mL, 4.83 mmol) at ambient temperature and stirred for 15 minutes. The mixture was cooled to 0° C. followed by addition of iodobenzene diacetate (IBD; 1.87 g, 5.80 mmol). The reaction was warmed to ambient temperature and stirred overnight. Additional IBD (0.8 equivalents, 4.64 mmol) was added and the reaction was allowed to stir at ambient temperature for 48 hours total. The mixture was transferred to a separatory funnel, diluting with water and DCM. The organic phase was washed with saturated aqueous Na2SO3, followed by back extraction of the aqueous phase 2 times with DCM. The organics were combined and washed with brine, dried over Na2SO4, filtered and concentrated to a residue under reduced pressure, followed by purification by flash column chromatography to give the product (1.08 g, 57% yield). MS APCI (+) m/z 395.3 (M+1) detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987251B2
Source datasetuspto-grants-2015_03
ORD IDord-2b7e935582a74667b14622e10f3e2dc7
Source noteuspto-grants-2015_03