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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596096Generated: October 29, 2026

Hydrochloric Acid → 4-(6-(1-Acetylpiperidin-3-yl)-3-aminopyrazin-2-yl)-2-fluorobenzoic acid

https://huagongshe.com/reaction/596096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantMethyl 4-(6-(1-acetylpiperidin-3-yl)-3-aminopyrazin-2-yl)-2-fluorobenzoateHCID 118045778—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-(6-(1-Acetylpiperidin-3-yl)-3-aminopyrazin-2-yl)-2-fluorobenzoic acidHCID 118045982—

Reaction Steps

To a mixture of methyl 4-(6-(1-acetylpiperidin-3-yl)-3-aminopyrazin-2-yl)-2-fluorobenzoate (50 mg, 0.134 mmol) in THF (4 mL) and MeOH (2 mL) was added 1 M LiOH (0.500 mL, 0.500 mmol). The reaction mixture was stirred at room temperature for 4 h. The pH of reaction mixture was adjusted to ˜3 with 2 N HCl, and the product was extracted with ethyl acetate. The organic layer was separated, washed with brine, dried over sodium sulfate, filtered and evaporated. The residue was proceeded for next step without purification (34 mg, 70.7%). LCMS (m/z): 359.1 (MH+), 0.534 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-834bce8fda924b2ba5b7353b5f141803
Source noteuspto-grants-2016_01