Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630303Generated: November 1, 2026

Butanedioic acid, 2-acetyl-, 1,4-diethyl ester → HCID 178470702, compound

https://huagongshe.com/reaction/1630303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanedioic acid, 2-acetyl-, 1,4-diethyl esterHCID 66197—
ReactantHCID 178469278HCID 178469278—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventO-XyleneHCID 7237—
ProductHCID 178470702HCID 17847070275.3%

Reaction Steps

A suspension of ethyl 5-amino-1H-pyrazole-3-carboxylate (35.5 g, 229 mmol, prepared according to WO 2008015271), diethyl 2-acetylsuccinate (51.2 mL, 275 mmol) and Ts-OH.H2O (0.218 g, 1.144 mmol) in o-xylene (500 mL) was refluxed using Dean-Stork condensor for 5 h. (Note: The suspension turned clear homogeneous solution and then in about 15 min yellow solid started crashing out of the reaction). Then, the reaction mixture was cooled, diluted with hexanes (250 mL), filtered, washed with hexanes and dried to afford ethyl 6-(2-ethoxy-2-oxoethyl)-7-hydroxy-5-methylpyrazolo[1,5-a]pyrimidine-2-carboxylate (53 g, 75% yield) as light yellow solid. 1H NMR (500 MHz, DMSO-d6) δ: 12.61 (br. s., 1H), 6.49 (s, 1H), 4.34 (q, J=7.1 Hz, 2H), 4.09 (q, J=7.1 Hz, 2H), 3.57 (s, 2H), 2.34 (s, 3H), 1.33 (t, J=7.2 Hz, 3H), 1.19 (t, J=7.0 Hz, 3H). LCMS (M+H)=308.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791108B2
Source datasetuspto-grants-2014_07
ORD IDord-588ed7e576534ceca6aeffd1f2fddbf6
Source noteuspto-grants-2014_07