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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16877Generated: October 30, 2026

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

https://huagongshe.com/reaction/16877

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 numberUS07737149B2
Source datasetuspto-grants-2010_06
ORD IDord-1c56c91ad2b7476684f4bcc21be14b6a
Source noteuspto-grants-2010_06