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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521229Generated: October 30, 2026

Acetic Acid → HCID 86729398, compound

https://huagongshe.com/reaction/521229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetophenoneHCID 7410—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86729399HCID 86729399—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductHCID 86729398HCID 86729398—

Reaction Steps

To a solution of 1-(4-(cyanomethyl)piperidin-4-yl)-3-((4-fluorophenyl)amino)-1H-pyrazole-4-carboxamide (Intermediate #38-5) (50 mg, 0.11 mmol) in MeOH (0.32 mL) and DMF (0.063 mL) was added acetophenone (41 mg, 0.34 mmol) and acetic acid (0.065 mL, 1.1 mmol). The reaction mixture was allowed to stir at room temperature for 15 minutes. Sodium cyanoborohydride (7 mg, 0.1 mmol) was added and the reaction mixture was allowed to stir for 24 hours at ambient temperature. The mixture was then purified directly by mass-triggered reverse-phase preparative HPLC (MeCN/water, with 0.1% v/v TFA modifier). Desired fractions were identified, combined, and concentrated in vacuo. The residue was dissolved in MeOH and passed through a Si-Carbonate cartridge to afford the title compound as a free base.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328099B2
Source datasetuspto-grants-2016_05
ORD IDord-e0be047da1e5459796cd2224ddf10a50
Source noteuspto-grants-2016_05