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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264546Generated: November 1, 2026

Acetic Acid → HCID 16737506, compound

https://huagongshe.com/reaction/2264546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-Piperidinecarboxylic acidHCID 3773—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 59595889HCID 59595889—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethane methanolHCID 21226129—
ProductHCID 16737506HCID 1673750655%

Reaction Steps

A mixture of 4-(5-isobutylbenzofuran-2-yl)benzaldehyde (22 mg, 0.08 mmol), acetic acid (7 μL, 0.12 mmol) and piperidine-4-carboxylic acid (15 mg, 0.12 mmol) in DCM/MeOH (1:1, 1.4 mL) was stirred at room temperature for 1 h. Sodium cyanoborohydride (2.5 mg, 0.04 mmol) was added and the reaction mixture was stirred for 4 h at room temperature. After concentration of solvent under reduced pressure, the resulting residue was dissolved in an aliquot of DMSO and purified by reverse phase preparative HPLC (Phenomenex reverse phase Luna 5μ C18(2) column, 60×21.2 mm ID) to yield the desired final product (1 6.9 mg, 55%): >95% purity by LCMS, ESI-MS: 392.0 (M+H)+, 1H NMR (400 MHz, CD3OD) δ 8.01 (d, 2H), 7.59 (d, 2H), 7.43 (d, 1H), 7.39 (s, 1H), 7.26 (s, 1H), 7.13 (dd, 1H), 4.36 (s, 2H), 3.58(m, 2H), 3.10 (m, 2H), 2.65(m, 1H), 2.57 (d, 2H), 1.90 (m, 1H), 0.92 (d, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855193B2
Source datasetuspto-grants-2010_12
ORD IDord-302de4a1b80f43648c8ec5e2e0ceed67
Source noteuspto-grants-2010_12