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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 655312Generated: October 25, 2026

Triphenylphosphine → 3-(4-Methylpiperazin-1-yl)propyl [3-(5-methyl-2-oxooxazolo-[4,5-b]pyridin-3-ylmethyl)phenyl]carbamate

https://huagongshe.com/reaction/655312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantDi-tert-butyl azodicarboxylateHCID 97268—
Reactant5-Methyloxazolo[4,5-b]pyridin-2(3H)-oneHCID 10012075—
Reactant3-(4-Methylpiperazin-1-yl)propyl (3-hydroxymethylphenyl)carbamateHCID 59564727—
SolventDimethylformamideHCID 6228—
Product3-(4-Methylpiperazin-1-yl)propyl [3-(5-methyl-2-oxooxazolo-[4,5-b]pyridin-3-ylmethyl)phenyl]carbamateHCID 59564715—

Reaction Steps

98 mg (0.65 mmol) of 5-methyl-3H-oxazolo[4,5-b]pyridin-2-one, 200 mg (0.65 mmol) of 3-(4-methylpiperazin-1-yl)propyl (3-hydroxymethylphenyl)carbamate and 325 mg (0.98 mmol) of polymer-bound triphenylphosphine (3 mmol/g) are suspended in 5 ml of DMF, and the mixture is shaken for 30 min. 229 mg (0.98 mmol) of di-tert-butyl azodicarboxylate are subsequently added. The reaction mixture is shaken at room temperature. The reaction mixture is filtered and rinsed with THF, and the filtrate is evaporated. The residue is purified by column chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071593B2
Source datasetuspto-grants-2011_12
ORD IDord-829cde76b514485e9a04d8c2ab01967f
Source noteuspto-grants-2011_12