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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911981Generated: October 28, 2026

Triphenylphosphine → HCID 57812426, compound

https://huagongshe.com/reaction/911981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
Reactant4-[4-(7-Hydroxy-6-nitrofuro[3,2-c]pyridin-3-yl)pyrazol-1-yl]piperidine-1-carboxylic acid tert-butyl esterHCID 57812534—
ReactantHCID 58659227HCID 58659227—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57812426HCID 57812426—

Reaction Conditions

Temperature40 °C

Reaction Steps

1-(2,6-Dichloro-3,5-difluorophenyl)ethanol (133 mg, 0.586 mmol), 4-[4-(7-Hydroxy-6-nitrofuro[3,2-c]pyridin-3-yl)-pyrazol-1-yl]-piperidine-1-carboxylic acid tert-butyl ester (250 mg, 0.52 mmol), PPh3 (410 mg, 1.60 mmol) and THF (20 mL) was added to a dry round bottom flask. Diisopropyl azodicarboxylate (320 mg, 1.60 mmol) was added and the reaction mixture was heated at 40° C. More DIAD (320 mg, 1.60 mmol) was then added and the reaction mixture was heated at 40° C. for 2 h. Purification by flash column chromatography using 10%→40% EtOAc in hexanes afforded the title compound as a yellow solid. MS (ES+): m/z 581.88/583.80 (100/80) [MH+−isobutene]. HPLC: tR=4.29 min (ZQ3, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022206B2
Source datasetuspto-grants-2011_09
ORD IDord-f262bc85d3714a4697c581bd6281b6e5
Source noteuspto-grants-2011_09