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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200116Generated: October 31, 2026

Cesium carbonate → tert-butyl N-[4-[[2-(cyclopropanecarbonylamino)-4-pyridyl]oxy]-2-fluoro-phenyl]carbamate

https://huagongshe.com/reaction/2200116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantCyclopropanecarboxamideHCID 80376—
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 118223438HCID 118223438—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl N-[4-[[2-(cyclopropanecarbonylamino)-4-pyridyl]oxy]-2-fluoro-phenyl]carbamateHCID 90019939213.2%

Reaction Steps

Dissolve tert-butyl N-[4-[(2-chloro-4-pyridyl)oxy]-2-fluoro-phenyl]carbamate (13 g, 14.7 mmol), cyclopropanecarboxamide (8.1 g, 36.7 mmol) in 1,4-dioxane (240 mL). Then add tris(dibenzylideneacetone)dipalladium(0) [Pd2(dba)3, 1.75 g, 0.73 mmol), (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (BINAP, 2.38 g, 1.47 mmol) and Cs2CO3 (24.8 g, 29.4 mmol) under N2. Stir the reaction at 100° C. for 12 hrs. Cool to room temperature, filter, and concentrate the filtrate to give the crude product. Purification by chromatography (silica gel, DCM:EtOAc-1:5) affords the title compound (12.14 g, 83.2%). MS: (M+1): 388.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359338B2
Source datasetuspto-grants-2016_06
ORD IDord-d429e7d2c4dc4b52b7dd67ea5e5a7f4f
Source noteuspto-grants-2016_06