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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81496Generated: October 26, 2026

2-Methylpentane → 3-Chloro-5-[2-methyl-5-(morpholine-4-sulfonyl)-phenyl]-pyrazin-2-ylamine

https://huagongshe.com/reaction/81496

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpentaneHCID 7892—
ReactantSodium CarbonateHCID 10340—
Reactant2-Methyl-5-(morpholin-4-ylsulphonyl)benzeneboronic acidHCID 44119554—
Reactant5-Bromo-3-chloropyrazin-2-amineHCID 46738202—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product3-Chloro-5-[2-methyl-5-(morpholine-4-sulfonyl)-phenyl]-pyrazin-2-ylamineHCID 86634554—

Reaction Steps

5-Bromo-3-chloro-pyrazin-2-ylamine (0.600 g, 2.88 mmol), 2-methyl-5-(N-morpholinylsulfonyl)phenylboronic acid (0.821 g, 2.88 mmol), 1,1′BIS(Diphenylphosphino-ferrocene)dichloropalladium (II) complex with DCM (0.118 g, 0.14 mmol), 2N Na2CO3 (aq.) (5 ml) and DME (15 ml) are stirred together at 100° C. for 1 hour. Product is purified by reverse phase chromatography and evaporation of the clean fractions yields a cream solid. The solid is dissolved in DCM (100 ml) and washed with 2N NaOH (aq.) (50 ml). The organic phase is dried over magnesium sulphate, filtered and the solvent evaporated to yield an orange semi-solid. This is dissolved ethyl acetate (10 ml) and iso-hexane is added. A precipitate forms and is filtered off to yield the title compound as an off white solid. [M+H]+ 410.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846687B2
Source datasetuspto-grants-2014_09
ORD IDord-4ca20ac305394febb9a15d8950b4d4c1
Source noteuspto-grants-2014_09