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HRID 2387226作成日:2026年10月27日

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

https://huagongshe.com/reaction/2387226

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethylpentaneHCID 7892—
反応物Sodium CarbonateHCID 10340—
反応物2-Methyl-5-(morpholin-4-ylsulphonyl)benzeneboronic acidHCID 44119554—
反応物5-Bromo-3-chloropyrazin-2-amineHCID 46738202—
溶媒DichloromethaneHCID 6344—
溶媒1,2-DimethoxyethaneHCID 8071—
溶媒Ethyl AcetateHCID 8857—
生成物3-Chloro-5-[2-methyl-5-(morpholine-4-sulfonyl)-phenyl]-pyrazin-2-ylamineHCID 86634554—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08268834B2
出典データセットuspto-grants-2012_09
ORD IDord-06aca14707174b80bf8a02755af6e412
出典メモuspto-grants-2012_09