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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234834Generated: October 25, 2026

1H-Pyrazol-3-amine, 5-methyl- → (6-Bromo-imidazo[1,2-a]pyrazin-8-yl)-(5-methyl-1H-pyrazol-3-yl)-amine

https://huagongshe.com/reaction/2234834

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrazol-3-amine, 5-methyl-HCID 93146—
Reactant6,8-Dibromoimidazo[1,2-a]pyrazineHCID 15025843—
SolventEthanolHCID 702—
Product(6-Bromo-imidazo[1,2-a]pyrazin-8-yl)-(5-methyl-1H-pyrazol-3-yl)-amineHCID 8623729532.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

Example 8 was then prepared as follows. 6,8-Dibromoimidazo[1,2-a]pyrazine (278 mg, 1 mmol) and 5-methyl-1H-pyrazol-3-amine (196 mg, 2 mmol) was suspended in EtOH (2 ml). The mixture was heated with microwave at 120° C. for four hours. The mixture was then purified with HPLC to give (6-Bromo-imidazo[1,2-a]pyrazin-8-yl)-(5-methyl-1H-pyrazol-3-yl)-amine as a solid (96 mg). 1H NMR (400 MHz, DMSO) δ 8.29 (s, 1H) 7.98 (s, 1H) 7.70 (s, 1H) 6.48 (s, 1H) 2.27 (s, 3H). [M+H] calc'd for C10H9BrN6, 293; found, 293.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713973B2
Source datasetuspto-grants-2010_05
ORD IDord-bcad8e67d9d040c8adfd8f318dde4daf
Source noteuspto-grants-2010_05