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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29100Generated: October 25, 2026

Perchloric Acid → [2-(5-Bromothiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-(1,1,3,3-tetramethyl-butyl)-amine

https://huagongshe.com/reaction/29100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPerchloric AcidHCID 24247—
Reactant1,1,3,3-Tetramethylbutyl isocyanideHCID 26725—
Reactant5-Bromothiophene-2-carbaldehydeHCID 78428—
ReactantAminopyrazineHCID 78747—
SolventChloroformHCID 6212—
Product[2-(5-Bromothiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-(1,1,3,3-tetramethyl-butyl)-amineHCID 6931681156%

Reaction Conditions

Temperature50 °C

Reaction Steps

4.76 g (50.0 mmol) of 2-aminopyrazine were dissolved together with 8.76 ml (50.0 mmol) of 1,1,3,3-tetramethyl-butylisonitrile and 5.42 ml (50.0 mmol) of 5-bromothiophene-2-carbaldehyde in chloroform (40 ml) After addition of perchloric acid (5 ml), the mixture was stirred at 50° C. for 16 h. After cooling to RT, washing was performed 2× with a sat. aq. sodium carbonate solution. The organic phase was dried over magnesium sulfate, filtered and evaporated under a vacuum. After carrying out column chromatography (EA/DCM 1:3) with the group, 11.39 g (28.0 mmol, 56% of theoretical) of [2-(5-bromothiophen-2-yl)-imidazo[1,2-a]pyrazin-3-yl]-(1,1,3,3-tetramethyl-butyl)-amine were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07420056B2
Source datasetuspto-grants-2008_09
ORD IDord-1a50e45d7d55499e974d1b28fd9e08c9
Source noteuspto-grants-2008_09