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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831598Generated: October 31, 2026

Ethyl pyruvate → HCID 69658157, compound

https://huagongshe.com/reaction/1831598

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl pyruvateHCID 12041—
ReactantHCID 69658135HCID 69658135—
SolventEthanolHCID 702—
ProductHCID 69658157HCID 69658157—

Reaction Conditions

Temperature100 °C

Reaction Steps

(R)-6-(2-Chloro-4-methoxy-phenyl)-N4-(2-methoxy-1-methyl-ethyl)-pyrimidine-4,5-diamine (0.26 g, 0.82 mmol) was diluted in ethanol (8 ml) and ethyl pyruvate was added (0.92 ml, 8.2 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 6.0 mg of (R)-4-(2-chloro-4-methoxy-phenyl)-8-(2-methoxy-1-methyl-ethyl)-6-methyl-8H-pteridin-7-one (Example 570a). 1H NMR (300 MHz, CDCl3) δ ppm 9.09 (s, 1 H), 7.43 (d, J=8.79 Hz, 1 H), 7.09 (d, J=2.56 Hz, 1 H), 6.97 (dd, J=8.79, 2.56 Hz, 1 H), 4.39 (m, 3H), 3.91 (s, 3 H), 3.73 (dd, J=10.07, 5.31 Hz, 2 H), 3.35 (s, 3H), 2.53 (s, 3 H), 1.62 (6, J=6.96 Hz, 3 H). MS (AP) 375.2 [(M+H)+, 100].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067658B2
Source datasetuspto-grants-2006_06
ORD IDord-9087bc3683df4a479340426781d05791
Source noteuspto-grants-2006_06