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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrazinium chlorideHCID 115031—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 3-cyano-4-oxopyrrolidine-1-carboxylateHCID 2756790—
SolventEthanolHCID 702—
Producttert-Butyl 3-amino-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylateHCID 11333571—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653059B2
Source datasetuspto-grants-2014_02
ORD IDord-4fff926f718a4d83b4b8008d58bdcee6
Source noteuspto-grants-2014_02