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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407685Generated: October 29, 2026

Ammonia → 2-Nitro-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine

https://huagongshe.com/reaction/407685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1-(2-bromoethyl)-5-(bromomethyl)-3-nitro-1H-pyrazoleHCID 57502083—
SolventTetrahydrofuranHCID 8028—
Product2-Nitro-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazineHCID 5804427976%

Reaction Steps

A 250-mL single-neck round-bottomed flask equipped with a magnetic stirrer was charged with 124c (3.0 g, 9.64 mmol) in THF (35 mL) and aqueous ammonia (135 mL, 25-28%). The mixture was stirred at room temperature for 72 h under nitrogen. The reaction mixture was then concentrated under reduced pressure and the resulting residue was partitioned between ethyl acetate (100 mL) and water (100 mL). The aqueous layer was extracted with ethyl acetate (2×50 mL). The combined organic layer was washed with 10% potassium carbonate (2×100 mL), brine (200 mL), and dried over sodium sulfate. The drying agent was removed by filtration, and the filtrate was concentrated under reduced pressure to afford 124d as a yellow solid (1.23 g, 76%). MS: [M+H]+ 169

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754077B2
Source datasetuspto-grants-2014_06
ORD IDord-b160e0339513419982a94cf4987a6196
Source noteuspto-grants-2014_06