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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171006Generated: October 31, 2026

Formaldehyde → 6-(2-fluoro-phenyl)-8-{5-[1-(1-methyl-piperidin-4-yl)-1H-pyrazol-4-yl]-pyridin-3-yl}-pyrido[2,3-b]pyrazine

https://huagongshe.com/reaction/2171006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 68293201HCID 68293201—
SolventFormic AcidHCID 284—
Product6-(2-fluoro-phenyl)-8-{5-[1-(1-methyl-piperidin-4-yl)-1H-pyrazol-4-yl]-pyridin-3-yl}-pyrido[2,3-b]pyrazineHCID 60199115—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 85 mg (0.15 mmol) 4-(4-{5-[6-(2-fluoro-phenyl)-pyrido[2,3-b]pyrazin-8-yl]-pyridin-3-yl}-pyrazol-1-yl)-piperidine-1-carboxylic acid tert-butyl ester in 0.5 ml formic acid was treated with 36 μl (0.45 mmol) 35% aqueous formaldehyde solution and heated to 80° C. The reaction mixture was stirred at this temperature for 4 hours. The volume of the reaction mixture was reduced under vacuum and 2 N aqueous NaOH was added. The resulting precipitate was filtered off, washed with water and dried. The residue was chromatographed on a silica gel column with dichloromethane/methanol as eluent yielding 6-(2-fluoro-phenyl)-8-{5-[1-(1-methyl-piperidin-4-yl)-1H-pyrazol-4-yl]-pyridin-3-yl}-pyrido[2,3-b]pyrazine as off-white solid; HPLC/MS: 1.47 min, [M+H] 466.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051318B2
Source datasetuspto-grants-2015_06
ORD IDord-028a57c094c9467a879ec3beca7bcc20
Source noteuspto-grants-2015_06