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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403224Generated: November 1, 2026

Acetic Acid → 4-Piperidinecarboxylic acid

https://huagongshe.com/reaction/2403224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86663314HCID 86663314—
SolventMethanolHCID 887—
Product4-Piperidinecarboxylic acidHCID 3773—

Reaction Steps

Sodium cyanoborohydride (32.5 mg; 0.517 mmol) was added to a solution of 4-(5-(1-cyclohexyl-5-(methoxymethyl)-1H-pyrazol-4-yl)-1,2,4-oxadiazol-3-yl)benzaldehyde, obtained from step 1, (172 mg; 0.47 mmol) and isonipecotic acid (121.4 mg; 0.94 mmol) in a mixture of methanol (3 mL) and acetic acid (80.7 μl; 0.141 mmol) and the mixture was stirred at room temperature overnight. The solvent was removed in vacuo and the residue purified by preparative HPLC to give Example 64 as a white solid. 1H NMR (DMSO-d6) δ 8.23 (1 H, s), 8.04 (2 H, d, J=8.1 Hz), 7.54 (2 H, d, J=8.0 Hz), 5.02 (2 H, s), 4.44-4.34 (1 H, m), 3.56 (2 H, s), 3.34 (3 H, s), 2.78 (2 H, d, J=11.0 Hz), 2.26-2.17 (1 H, m), 2.06 (2 H, t, J=11.2 Hz), 1.96-1.76 (8 H, m), 1.71 (1 H, d, J=12.8 Hz), 1.66-1.52 (2 H, m), 1.53-1.37 (2 H, m), 1.25 (1 H, t, J=13.0 Hz). LC/MS: 480 (M+H)+. HPLC (Method G) Rt=2.39 min (Purity: 96.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802663B2
Source datasetuspto-grants-2014_08
ORD IDord-d9339b1d71b14cad84b1696a0c05f6ad
Source noteuspto-grants-2014_08