Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474212Generated: November 1, 2026

Triphenylphosphine → HCID 46836199, compound

https://huagongshe.com/reaction/474212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
ReactantCyclopentane-1,3-diolHCID 100165—
ReactantHCID 59438049HCID 59438049—
SolventDimethylformamideHCID 6228—
ProductHCID 46836199HCID 46836199—

Reaction Steps

100 mg (0.28 mmol) of 2-[3-(5-hydroxypyrimidin-2-yl)benzyl]-6-(1-methyl-1H-pyrazol-4-yl)-2H-pyridazin-3-one are dissolved in 6 ml of DMF, and 277 mg (0.83 mmol) of polymer-bound triphenylphosphine (3 mmol/g) and 33 mg (0.32 mmol) of 1,3-cyclopentanediol are added. The reaction mixture is shaken at room temperature for 15 min, and 196 mg (0.83 mmol) of di-tert-butyl azodicarboxylate are subsequently added. The reaction mix-ture was shaken at room temperature for 3 h, a further 277 mg (0.83 mmol) of polymer-bound triphenylphosphine (3 mmol/g) and 196 mg (0.83 mmol) of di-tert-butyl azodicarboxylate were added, and the mixture was shaken at room temperature for 18 h. The reaction mixture is filtered off through kieselguhr with suction and washed with acetonitrile. The filtrate is evaporated and purified by means of preparative HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637518B2
Source datasetuspto-grants-2014_01
ORD IDord-e9eb59344b0d42c0b317ad287184d618
Source noteuspto-grants-2014_01