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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930637Generated: October 30, 2026

Sodium ethoxide → HCID 178432899, compound

https://huagongshe.com/reaction/1930637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
Reactant1-tert-Butyl 3-methyl 4-oxopiperidine-1,3-dicarboxylateHCID 11276893—
ReactantHCID 178432900HCID 178432900—
SolventEthanolHCID 702—
ProductHCID 178432899HCID 17843289955.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

1-(4-(2-Methyl-1H-imidazol-1-yl)phenyl)guanidine (1.8 g, 8.36 mmol, example 9e), 1-tert-butyl 3-methyl 4-oxopiperidine-1,3-dicarboxylate (2.151 g, 8.36 mmol) and sodium ethoxide (0.569 g, 8.36 mmol) in ethanol (10 mL) were charged in a thick glass vial, which was sealed and heated under microwave irradiation at 110° C. for 2 h. The reaction mixture was allowed to reach room temperature and the solvent was evaporated under reduced pressure. The crude was dissolved in ethyl acetate and washed with water. The organic phase was dried under MgSO4 and concentrated under reduced pressure yielding tert-butyl 4-hydroxy-2-(4-(2-methyl-1H-imidazol-1-yl)phenylamino)-7,8-dihydropyrido[4,3-d]pyrimidine-6(5H)-carboxylate (1.970 g, 55.8%). The product was used as such in the subsequent step. MS (ES+) m/z 423.3 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188101B2
Source datasetuspto-grants-2012_05
ORD IDord-50a96eb31267441f83367386a702be67
Source noteuspto-grants-2012_05