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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958591Generated: October 27, 2026

Acetic Acid → (5-bromo-pyrazin-2-yl)-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)amine

https://huagongshe.com/reaction/1958591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-Amino-5-bromopyrazineHCID 599539—
Reactant1,3-dimethyl-1H-pyrazole-4-carbaldehydeHCID 847285—
ReactantBorane,N-dimethylmethanamine (1:1)HCID 6327651—
SolventEthyl AcetateHCID 8857—
Product(5-bromo-pyrazin-2-yl)-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)amineHCID 8661430392.9%

Reaction Steps

A mixture of 1,3-dimethyl-1H-pyrazole-4-carbaldehyde (142 mg, 1.145 mmol), 2-amino-5-bromopyrazine (200 mg, 1.149 mmol), borane trimethylamine complex (126 mg, 1.73 mmol) and glacial acetic acid (137 mg, 2.29 mmol) in anhydrous methonol (3 ml) was stirred at room temperature overnight. The reaction mixture was then diluted with ethyl acetate, washed with water, dried over MgSO4 and filtered. The filtrate was concentrated to give 300 mg of (5-bromo-pyrazin-2-yl)-(1,3-dimethyl-1H-pyrazol-4-ylmethyl)amine as crude product, which was used for next step reaction without further purification. Crude yield: 93%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410121B2
Source datasetuspto-grants-2013_04
ORD IDord-d31f5667466b43db91b5932cf3a42704
Source noteuspto-grants-2013_04