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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785833Generated: October 31, 2026

3-Pyridinecarboxaldehyde → HCID 22730881, compound

https://huagongshe.com/reaction/1785833

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinecarboxaldehydeHCID 10371—
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22730872HCID 22730872—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 22730881HCID 22730881—

Reaction Steps

A mixture of Example 340A (65 mg, 0.1 mmol), NaBH3CN (48 mg, 0.75 mmol), 2N NaOH (0.15 mL), and 3-pyridinecarboxaldehyde (214 mg, 2 mmol) in acetic acid (0.5 mL) and methanol (1 mL) was stirred for 16 hours. The reaction mixture was concentrated, dissolved in 1:1 DMSO/methanol (1.0 mL) and purified by reverse phase preparative HPLC using 20-90% acetonitrile/water containing 0.1% TFA to provide the desired product. MS (ESI(−)) m/e 628 (M−H)−; 1H NMR (300 MHz, DMSO-d6) δ 8.78 (br t, 1H), 8.70 (d, 1H), 8.70 (dd, 1H), 8.60 (d, 1H), 8.05 (m, 1H), 7.95 (d, 2H), 7.62 (d, 2H), 7.60 (dd, 1H), 7.40-7.15 (m, 6H), 6.35 (m, 1H), 4.52 (d, 2H), 3.92 (m, 4H),3.45 (t, 4H), 2.82 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504512B2
Source datasetuspto-grants-2009_03
ORD IDord-12b7908ed45c4f35a99a109b781a7540
Source noteuspto-grants-2009_03