Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605974Generated: October 30, 2026

Diisopropylethylamine → 5-Bromo-N-[4-(4-tert-butylpiperazin-1-yl)phenyl][1,2,4]triazolo[1,5-a]pyrazin-8-amine

https://huagongshe.com/reaction/605974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(4-tert-Butylpiperazin-1-yl)anilineHCID 24279182—
Reactant5,8-Dibromo-(1,2,4)triazolo(1,5-a)pyrazineHCID 49758022—
Reactant4-{8-[4-(4-Methyl-piperazin-1-yl)-phenylamino]-[1,2,4]triazolo[1,5-a]pyrazin-5-yl}-thiophene-2-carboxylic acid amideHCID 57589928—
SolventIsopropanolHCID 3776—
Product5-Bromo-N-[4-(4-tert-butylpiperazin-1-yl)phenyl][1,2,4]triazolo[1,5-a]pyrazin-8-amineHCID 5758999492.4%

Reaction Steps

This compound may be prepared using methods as described for Compound 6, step 1, using 5,8-dibromo-[1,2,4]triazolo[1,5-a]pyrazine (0.308 g, 1.107 mmol), 4-(4-tert-butyl-piperazin-1-yl)-phenylamine (0.310 g, 1.33 mmol) and N-ethyldiisopropyl-amine (0.289 mL, 1.66 mmol) in 2-propanol (5 mL). The reaction mixture is partitioned between DCM and 1N NaOH, the organic layer is separated and washed with water and brine, dried over MgSO4, filtered and concentrated under vacuum. Trituration of the residue with diethyl ether and petroleum ether affords the title compound (440 mg, 92%) as a cream solid. LCMS: Rt 2.25 min (96%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915256B2
Source datasetuspto-grants-2011_03
ORD IDord-7122b2b843d94772af4a1fdbcd09863c
Source noteuspto-grants-2011_03