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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831596Generated: November 2, 2026

Ethyl pyruvate → HCID 10022092, compound

https://huagongshe.com/reaction/1831596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl pyruvateHCID 12041—
ReactantHCID 69658167HCID 69658167—
SolventEthanolHCID 702—
ProductHCID 10022092HCID 10022092—

Reaction Conditions

Temperature100 °C

Reaction Steps

(R)-6-(2-Chloro-4-methoxy-phenyl)-N4-(1-cyclopropyl-ethyl)-pyrimidine-4,5-diamine (0.20 g, 0.52 mmol) was diluted in ethanol (5 ml) and ethyl pyruvate was added (0.58 ml, 5.2 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 2.0 mg of (R)-4-(2-chloro-4-methoxy-phenyl)-8-(1-cyclopropyl-ethyl)-6-methyl-8H-pteridin-7-one (Example 565a). 1H NMR (300 MHz, CDCl3) δ ppm 9.04 (s, 1 H), 7.45 (d, J=8.42 Hz, 1 H), 7.09 (d, J=2.56 Hz, 1 H), 6.98 (dd, J=8.42, 2.56 Hz, 1 H), 4.26 (m, 1 H), 3.91 (s, 3 H), 2.54 (d, J=7.32, 3 H), 2.18 (m, 3 H), 0.87 (m, 2 H), 0.45 (m, 2 H), 0.26 (m, 1 H). MS (AP) 371.3 [(M+H)+, 100].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067658B2
Source datasetuspto-grants-2006_06
ORD IDord-14d4067f353141c9871820933f0c57f8
Source noteuspto-grants-2006_06