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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926003Generated: November 1, 2026

Tributylphosphine → HCID 57597284, compound

https://huagongshe.com/reaction/1926003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactantdiazenedicarboxylic acid bis(N,N-piperidide)HCID 5702657—
ReactantHCID 57597147HCID 57597147—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 57597284HCID 5759728475.6%

Reaction Steps

To a suspension of 2-[4-({3-methyl-4-[(6-methylpyridin-3-yl)oxy]phenyl}amino)-5H-pyrrolo[3,2-d]pyrimidin-5-yl]ethanol (50 mg) and tributylphosphine (54 mg) in toluene (2.5 mL) was added 1,1′-[(E)-diazene-1,2-diyldicarbonyl]dipiperidine (67 mg), and the mixture was stirred at room temperature for 3 hrs. The reaction mixture was diluted with water (15 mL) and extracted with ethyl acetate (20 mL×3). The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was subjected to silica gel column chromatography (basic silica gel, eluent:ethyl acetate/methanol=100/0→90/10). The object fraction was concentrated under reduced pressure and dried to give the title compound (36 mg) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178543B2
Source datasetuspto-grants-2012_05
ORD IDord-f5a4c8e3a8c9460ba0b5bb6dafb0d551
Source noteuspto-grants-2012_05