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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911449Generated: November 1, 2026

Acetic Acid → Methyl 2-(1-methylpiperidin-4-yl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/1911449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 66589876HCID 66589876—
SolventMethanolHCID 887—
ProductMethyl 2-(1-methylpiperidin-4-yl)pyrimidine-5-carboxylateHCID 6658981094.8%

Reaction Steps

Sodium triacetoxyborohydride (532 mg, 2.51 mmol) was added to methyl 2-(piperidin-4-yl)pyrimidine-5-carboxylate (222 mg, 1.00 mmol), formaldehyde (37% aqueous solution, 1.50 ml, 20.07 mmol) and acetic acid (0.115 ml, 2.01 mmol) in methanol (4.994 ml) at 25° C. The resulting solution was stirred at ambient temperature for 3 days. The reaction mixture was diluted with methanol (20 mL) and the crude product was purified by ion exchange chromatography, using an SCX column. The desired product was eluted from the column using 7M NH3/MeOH and evaporated to dryness to afford methyl 2-(1-methylpiperidin-4-yl)pyrimidine-5-carboxylate (223 mg, 94%) as a cream waxy solid. This was used directly with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604022B2
Source datasetuspto-grants-2013_12
ORD IDord-691b79117a1b4da190ee5622f8fa6ba3
Source noteuspto-grants-2013_12