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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552114Generated: October 29, 2026

Hydrochloric Acid → 2-Aminopyrimidine-4-carbaldehyde

https://huagongshe.com/reaction/552114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(dimethoxymethyl)pyrimidin-2-amineHCID 4913032—
SolventEthyl AcetateHCID 8857—
Product2-Aminopyrimidine-4-carbaldehydeHCID 1783234637.3%

Reaction Steps

A solution of 2.5 g (15 mmol, 1.0 eq.) of 2-aminopyrimidine-4-carboxaldehyde dimethylacetal (I-8) in 16 mL (48 mmol, 3.2 eq.) of 3M HCl was heated at 48° C. for 14 h. The mixture was allowed to cool to room temperature and diluted with 50 mL of EtOAc. The aqueous layer was neutralized with NaHCO3 and then extracted with EtOAc (5×50 mL). The combined organic extracts were dried (Na2SO4) and the solvent removed in vacuo to provide 0.69 g (5.6 mmol, 37%) of 2-aminopyrimidine-4-carboxaldehyde (I-9) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951803B2
Source datasetuspto-grants-2011_05
ORD IDord-8d1c69c2c51a44118c5950aa007bf96e
Source noteuspto-grants-2011_05