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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508039Generated: October 27, 2026

Triphenylphosphine → methyl 3-(4-{(4-{[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]methoxy}benzyl)[(2-nitrophenyl)sulfonyl]amino}phenyl)propanoate

https://huagongshe.com/reaction/508039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantMethyl 3-(4-{[(2-nitrophenyl)sulfonyl]amino}phenyl)propanoateHCID 23157467—
Reactant(4-{[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]methoxy}phenyl)methanolHCID 23157546—
SolventDichloromethaneHCID 6344—
Productmethyl 3-(4-{(4-{[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]methoxy}benzyl)[(2-nitrophenyl)sulfonyl]amino}phenyl)propanoateHCID 23157545—

Reaction Steps

To a solution of methyl 3-(4-{[(2-nitrophenyl)sulfonyl]amino}phenyl)propanoate (182 mg, 0.5 mmol), (4-{[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]methoxy}phenyl)methanol (156 mg, 0.5 mmol) and triphenylphosphine (262 mg, 1.0 mmol) in dichloromethane (5 mL) was added diethyl azodicarboxylate (40% toluene solution, 435 mg, 1.0 mmol) at room temperature, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was purified by silica gel column chromatography (10%-80% ethyl acetate/hexane) to give a yellow oil containing the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-f90ccc57474d4b3e99741d436c995394
Source noteuspto-grants-2010_08