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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595099Generated: October 29, 2026

Tri-tert-butylphosphine tetrafluoroborate → methyl 8-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-pyrazolo[5,1-a]isoquinoline-7-carboxylate

https://huagongshe.com/reaction/595099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
ReactantMethyl 8-(2-bromo-4-fluorobenzenesulfonylamino]-pyrazolo[5,1-a]isoquinoline-7-carboxylateHCID 70984312—
ReactantN,N-diethyl-N-((Z)-1-tributylstannanylprop-1-en-3-yl)amineHCID 86684726—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Productmethyl 8-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-pyrazolo[5,1-a]isoquinoline-7-carboxylateHCID 8671281227.3%

Reaction Steps

A mixture of methyl 8-(2-bromo-4-fluorobenzenesulfonylamino]-pyrazolo[5,1-a]isoquinoline-7-carboxylate (Intermediate 2, 0.103 g), tris-(dibenzylideneacetone)-dipalladium (0) (0.025 g), tri-tert-butylphosphonium tetrafluoroborate (0.0127 g) and N,N-diethyl-N—((Z)-1-tributylstannanylprop-1-en-3-yl)-amine (Intermediate 3, 0.265 g) in dioxane (3 mL) was irradiated in the microwave at 80° C. for 2 hours. After cooling, the mixture was diluted with ethyl acetate and filtered through Celite. The filtrate was concentrated in vacuo and the residue was purified by chromatography on silica, eluting with a mixture of methanol and DCM with a gradient of 0-20% to give methyl 8-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonylamino]-pyrazolo[5,1-a]isoquinoline-7-carboxylate (0.030 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242997B2
Source datasetuspto-grants-2016_01
ORD IDord-101f81e24a1848abb6d131c79ccad484
Source noteuspto-grants-2016_01