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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943900Generated: November 2, 2026

Acetic Acid → HCID 67088839, compound

https://huagongshe.com/reaction/1943900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetaldehydeHCID 177—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 178509234HCID 178509234—
SolventEthyl AcetateHCID 8857—
SolventHCID 21943919HCID 21943919—
ProductHCID 67088839HCID 6708883916%

Reaction Steps

Acetaldehyde (0.258 g, 5.86 mmol) and a drop of acetic acid were added to a solution of 5-nitro-1H-pyrazolo[3,4-b]pyridin-3-amine (0.105 g, 0.586 mmol) in THF/dichloroethane (“DCE”) (12 mL, 1:1). NaBH(OAc)3 (1.24 g, 5.86 mmol) was added, and the mixture was left at room temperature for 60 hours. The reaction mixture was diluted with ethyl acetate (50 mL) and quenched with water (10 mL). The aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic layers were dried, filtered and concentrated. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (9:1), hexanes/ethyl acetate (4:1) to give N,N-diethyl-5-nitro-1H-pyrazolo[3,4-b]pyridin-3-amine (22 mg, 16% yield) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394795B2
Source datasetuspto-grants-2013_03
ORD IDord-59d45b8d87164ee9805d83e832e37e73
Source noteuspto-grants-2013_03