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HRID 1912178作成日:2026年10月25日

3-(Piperidinosulfonyl)aniline → 5-Methyl-N2-[3-(piperidine-1-sulfonyl)-phenyl]-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/1912178

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Piperidinosulfonyl)anilineHCID 2794791—
反応物2-Chloro-5-methylpyrimidin-4-amineHCID 4302175—
溶媒Acetic AcidHCID 176—
生成物5-Methyl-N2-[3-(piperidine-1-sulfonyl)-phenyl]-pyrimidine-2,4-diamineHCID 57675084—

反応手順

A mixture of 2-chloro-5-methyl-pyrimidin-4-ylamine (0.25 g, 1.74 mmol) and 3-(piperidine-1-sulfonyl)-phenylamine (0.50 g, 2.1 mmol) in acetic acid (4 mL) was sealed in a microwave reaction tube and irradiated with microwave at 130° C. for 15 min. After cooling to room temperature, the cap was removed and the mixture concentrated. The residue was taken in water (20 mL) and pH adjusted to ˜9 with 10% NaOH solution. The resulting solution was extracted with EtOAc (2×30 mL) and the organic layer separated. The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and filtered. The filtrate was concentrated in vacuo and the crude product (˜0.6 g) used in the next step without purification. MS (ES+): m/z 348 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08604042B2
出典データセットuspto-grants-2013_12
ORD IDord-cbbdf84f0ec2410c938931ee38d66137
出典メモuspto-grants-2013_12