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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 921065Generated: October 27, 2026

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

https://huagongshe.com/reaction/921065

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 TsOH.H2O (0.218 g, 1.144 mmol) in o-xylene (500 mL) was refluxed using a Dean-Stork condenser for 5 h. (Note: The suspension turned into a clear homogeneous solution and then in about 15 min a yellow solid started precipitated out of solution). 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+1)=308.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273067B2
Source datasetuspto-grants-2016_03
ORD IDord-f2953e4e0a7e497197991f14d8aceb69
Source noteuspto-grants-2016_03