HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947718Generated: October 31, 2026
HCID 57907463, compound → HCID 57907386, compound
https://huagongshe.com/reaction/1947718
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57907463 | HCID 57907463 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57907386 | HCID 57907386 | 97.3% |
Reaction Steps
A 100 mL round bottom flask under an atmosphere of nitrogen was charged with 0.600 mg (0.560 mmol) of 10 weight percent palladium on activated carbon and wet with 10 mL of ethanol. Next, a solution of 6.0 g (0.025 mol) of benzyl 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole-6-carboxylate from step F above in 40 mL of ethanol was added and the mixture placed under 1 atmosphere of hydrogen. The reaction was stirred for 3 h then filtered through a pad of Celite®. The pad was washed with 20 mL of ethanol and the filtrate was evaporated in vacuo to afford the title compound as a colorless solid (3.7 g, quantitative yield). 1H NMR (500 MHz, DMSO-d6): δ 11.90 (br s, 1H), 7.44 (s, 1H), 5.98 (s, 1H), 4.87 (dd, J=8.9, 3.7 Hz, 1H), 2.94-2.82 (m, 3H), 2.58-2.52 (m, 1H). LC-MS: m/z (ES) 153 (MH)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399480B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-38b8f6cd353a446f8b72f1911ced84bd |
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| Source note | uspto-grants-2013_03 |
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