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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908487Generated: October 29, 2026

Cesium fluoride → HCID 67388157, compound

https://huagongshe.com/reaction/908487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium fluorideHCID 25953—
Reactanttert-butyl 4-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]piperidine-1-carboxylateHCID 45480279—
ReactantHCID 67388746HCID 67388746—
CatalystHCID 178418476HCID 178418476—
SolventMethanolHCID 887—
ProductHCID 67388157HCID 6738815769.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of bis(triphenylphosphine)palladium chloride (17.69 mg) was added to tert-butyl 4-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazol-1-yl]piperidine-1-carboxylate (380 mg), methyl 2-(2-amino-5-bromo-3-pyridyl)-1,3-benzoxazole-7-carboxylate (390 mg) and caesium fluoride (459 mg) dissolved in degassed methanol (5 ml) under argon. The resulting slurry was heated at 120° C. in the microwave for 30 minutes. The mixture was adsorbed on silica gel. The crude product was purified by flash chromatography on silica gel eluting with 1 to 4% methanol in dichloromethane. The solvent was evaporated to dryness to afford methyl 2-[2-amino-5-[1-(1-tert-butoxycarbonyl-4-piperidyl)pyrazol-4-yl]-3-pyridyl]-1,3-benzoxazole-7-carboxylate (365 mg) as a pale yellow solid. NMR Spectrum: (CDCl3) 1.49 (s, 9H), 1.97 (dd, 1H), 2.02 (dd, 1H), 2.16-2.23 (m, 2H), 2.84-3.01 (m, 2H), 4.06 (s, 3H), 4.19-4.40 (m, 3H), 6.88 (bs, 2H), 7.44 (dd, 1H), 7.70 (s, 1H), 7.80 (s, 1H), 7.94 (dd, 1H), 8.01 (dd, 1H), 8.40 (d, 1H), 8.48 (d, 1H); Mass spectrum: M+H+ 519;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017611B2
Source datasetuspto-grants-2011_09
ORD IDord-920b444d046f48b9a54d0436768779f9
Source noteuspto-grants-2011_09