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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535412Generated: November 2, 2026

Cesium fluoride → HCID 86694398, compound

https://huagongshe.com/reaction/535412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactant3,5-Dimethylisoxazole-4-boronic acidHCID 2734346—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
ReactantHCID 86694399HCID 86694399—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86694398HCID 86694398—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of tert-butyl-N-[1-[[5-bromo-6-(2-isoquinolin-6-ylethynyl)pyridin-2-yl]amino]-1-oxopropan-2-yl]-N-methylcarbamate C2b (300 mg, 0.59 mmol), (3,5-dimethyl-1,2-oxazol-4-yl)boronic acid (166 mg, 1.18 mmol), CsF (358 mg, 2.36 mmol) tris-(dibenzylideneacetone)dipalladium(0) (41 mg, 0.06 mmol), tri-tert-butylphosphonium tetrafluoroborate (34 mg, 0.12 mmol) and dioxane (4.5 ml) is stirred under argon atmosphere at 50° C. for 2 h. The mixture is diluted with DCM and extracted with a saturated aqueous solution of NaHCO3. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by RP HPLC. Yield: 191 mg (62%). HPLC-MS: M+H=526; tR=1.89 min (*Method—2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859541B2
Source datasetuspto-grants-2014_10
ORD IDord-56f38fd93b6542f0a1d4636985c8f478
Source noteuspto-grants-2014_10