Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043451Generated: October 31, 2026

Aminopyrazine → HCID 70672079, compound

https://huagongshe.com/reaction/2043451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminopyrazineHCID 78747—
Reactant2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 86659402HCID 86659402—
SolventTolueneHCID 1140—
ProductHCID 70672079HCID 7067207973.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

95 mg of (S)-6-chloro-N-[1-(4-fluorophenyl)ethyl]-4-methylpyridine-2-amine, 40 mg of 2-aminopyrazine, 34 mg of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl, 48 mg of sodium t-butoxide and 19 mg of tris(dibenzylideneacetone)(chloroform)dipalladium were added in turn to 6 ml of degassed toluene, and the mixture was stirred at 100° C. for 1 hour under argon atmosphere. The reaction solution was purified by silica gel column chromatography to obtain 85 mg of (S)—N2-[1-(4-fluorophenyl)ethyl]-4-methyl-N6-(pyrazin-2-yl)pyridine-2,6-diamine. Furthermore, the obtained compound was subjected to hydrochlorination using a conventional method to obtain 38 mg of the objective compound as yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586591B2
Source datasetuspto-grants-2013_11
ORD IDord-f9af99b826bb4f2fb6258663fd826199
Source noteuspto-grants-2013_11