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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337309Generated: October 29, 2026

5-Ethyl-2-nitro-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazine → 5-Ethyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-amine

https://huagongshe.com/reaction/337309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Ethyl-2-nitro-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazineHCID 58043925—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-Ethyl-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-amineHCID 5804394897%

Reaction Steps

In a 250 mL round-bottomed flask, 5-ethyl-2-nitro-4,5,6,7-tetrahydro -pyrazolo[1,5-a]pyrazine (427 mg, 2.17 mmol, Eq: 1.00) was combined with EtOH (50 ml) to give a light yellow suspension. The reaction mixture was vacuum flushed three times with argon then 10% Pd/C (115 mg, 1.08 mmol, Eq: 0.5) was added and the reaction mixture was stirred under hydrogen balloon overnight. The reaction was filtered through a pad of celite. The celite pad was washed with ethanol. The combined filtrate and washes were concentrated in vacuo to afford the desired product (350 mg). (M+H)+=167 m/e. 1H NMR (300 MHz, CHLOROFORM-d) δ ppm 1.16 (t, J=7.18 Hz, 3 H) 2.59 (q, J=7.18 Hz, 2 H) 2.79-3.03 (m, 2 H) 3.57 (overlapping s, 4 H) 3.87-4.12 (m, 2 H) 5.35 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889682B2
Source datasetuspto-grants-2014_11
ORD IDord-419404430aaa40b6b9aeb1a97f1b2c1c
Source noteuspto-grants-2014_11