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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406215Generated: November 1, 2026

Sodium ethoxide → HCID 178451642, compound

https://huagongshe.com/reaction/2406215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantMethanimidamide, hydrochloride (1:1)HCID 10313058—
Reactant1-tert-Butyl 4-ethyl 3-oxopiperidine-1,4-dicarboxylateHCID 15852989—
SolventEthanolHCID 702—
ProductHCID 178451642HCID 17845164242.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

3-Oxo-piperidine-1,4-dicarboxylic acid 1-tert-butyl ester 4-ethyl ester (4.6 g, 16.8 mmol) was dissolved in EtOH (90 mL), and sodium ethoxide (2.3 g, 33.6 mmol) and formamidine hydrochloride (2.0 g, 25.2 mmol) were sequentially added. The resulting suspension was heated to 70° C. and stirred for 5 hours, and then the reaction mixture was cooled to room temperature and concentrated. The residue was dissolved in saturated ammonium chloride and extracted with ethyl acetate. The aqueous phase was adjusted to pH ˜5.5 using concentrated AcOH, and extracted several more times with ethyl acetate. The combined organic layers were sequentially washed with water and brine, dried, and concentrated to afford 4-hydroxy-5,8-dihydro-6H-pyrido[3,4-d]pyrimidine-7-carboxylic acid tert-butyl ester as a brown solid (1.8 g, 42% yield). MS (ESI) m/e (M+H+)=251.28

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809352B2
Source datasetuspto-grants-2014_08
ORD IDord-4d57dc5ab3ca4e52953c84e6bac2be92
Source noteuspto-grants-2014_08