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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butanedioic acid, 2-acetyl-, 1,4-diethyl ester | HCID 66197 | — |
| Reactant | HCID 178469278 | HCID 178469278 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178470702 | HCID 178470702 | 75.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791108B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-588ed7e576534ceca6aeffd1f2fddbf6 |
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| Source note | uspto-grants-2014_07 |
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