HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241564Generated: October 29, 2026
Water → tert-Butyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate
https://huagongshe.com/reaction/241564
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hydrazinium chloride | HCID 115031 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | tert-Butyl 3-cyano-4-oxopyrrolidine-1-carboxylate | HCID 2756790 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate | HCID 11333571 | — |
Reaction Steps
N-Boc-3-cyano-4-pyrrolidinone (5 g, 23.78 mmol) and hydrazine monohydrochloride (1.629 g, 23.78 mmol) were dissolved in ethanol (140 ml). The mixture was heated to 60° C. for 3 h. The mixture was cooled to 0° C. and saturated aqueous NaHCO3 (50 mL) was added slowly, remaining water was extracted four times with ethyl acetate. The organic phase was dried over Na2SO4 (anhydrous). The residue was purified by column chromatography on silica gel Biotage 40M, eluting with EtOAc/MeOH/aqueous ammonia (gradient from 0 to 10%) to give the title product as a yellow foam. LC-MS: 224.99 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08653059B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-4fff926f718a4d83b4b8008d58bdcee6 |
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| Source note | uspto-grants-2014_02 |
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