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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400566Generated: November 1, 2026

Sodium Chlorite → 4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)furan-2-carboxylic acid

https://huagongshe.com/reaction/400566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
Reactant4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)furan-2-carbaldehydeHCID 57647399—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)furan-2-carboxylic acidHCID 5764741364.6%

Reaction Steps

600 mg [2.82 mMols] of 4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)furan-2-carbaldehyde was dissolved in 5.0 mL of DMSO/2.0 mL of water and stirred with 210 mg [1.75 mMols] of sodium dihydrogen phosphate, reducing the temperature as cold as possible so as not to effect crystallization. 532 mg sodium chlorite [5.88 mMols] in 4.0 mL of water was slowly added dropwise to this stirring solution. Solution was allowed to warm to ambient temperature and diluted with water to effect precipitation. The fine flocculent material was centrifuged down and washed with water and re-centrifuged. The oily pellet was transferred to a RB with acetonitrile and the solvents were removed under reduced pressure. The residue was stirred with a mixture of MTBE/acetonitrile (4:1) overnight and the powder isolated in the morning via suction filtration, washed with the same mixture and air dried. The material, (yield 64.6%) a beige powder, was utilized without further purification. LC/MS m+1 230/m−1 228.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741912B2
Source datasetuspto-grants-2014_06
ORD IDord-efe8b6c7aa3644a09102554290a76edc
Source noteuspto-grants-2014_06