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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | 4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)furan-2-carbaldehyde | HCID 57647399 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)furan-2-carboxylic acid | HCID 57647413 | 64.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08741912B2 |
|---|
| Source dataset | uspto-grants-2014_06 |
|---|
| ORD ID | ord-efe8b6c7aa3644a09102554290a76edc |
|---|
| Source note | uspto-grants-2014_06 |
|---|