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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831595Generated: October 31, 2026

Ethyl pyruvate → HCID 11741745, compound

https://huagongshe.com/reaction/1831595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl pyruvateHCID 12041—
ReactantHCID 22052196HCID 22052196—
SolventEthanolHCID 702—
ProductHCID 11741745HCID 11741745—

Reaction Conditions

Temperature100 °C

Reaction Steps

6-(2-Chloro-4-methoxy-phenyl)-N4-(1-propyl-butyl)-pyrimidine-4,5-diamine (0.29 g, 0.83 mmol) was diluted in ethanol (8 ml) and ethyl pyruvate was added (0.92 ml, 8.3 mmol). The mixture was stirred for 18 hours at which time the solution was concentrated. The residue was diluted in glacial acetic acid (10 ml) and warmed to 100° C. for 1 hour. After concentrating the solution the product was purified by reverse phase HPLC to yield 13.5 mg of 4-(2-chloro-4-methoxy-phenyl)-6-methyl-8-(1-propyl-butyl)-8H-pteridin-7-one (Example 563). 1H NMR (300 MHz, CDCl3) δ ppm 9.02 (s, 1 H), 7.41 (d, J=8.42 Hz, 1 H), 7.05 (d, J=2.56 Hz, 1 H), 6.93 (dd, J=8.42, 2.56 Hz, 1 H), 3.86 (s, 3 H), 4.40 (m, 1H), 2.48 (m, 2 H), 2.31 (m, 2 H), 1.89 (m, 2 H), 1.19 (m, 5 H), 0.88 (t, J=7.32 Hz, 6 H). MS (AP) 321.2 [(M+H)+, 100]. MS (AP) 401.3 [(M+H)+, 100].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067658B2
Source datasetuspto-grants-2006_06
ORD IDord-4f8739aacf544758b419cc7ae2debace
Source noteuspto-grants-2006_06