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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 491197생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/491197

반응식

참여 물질

역할이름HCID투입량
반응물3-(Piperidinosulfonyl)anilineHCID 2794791—
반응물2-Chloro-5-methylpyrimidin-4-amineHCID 4302175—
용매Acetic AcidHCID 176—
생성물5-Methyl-N2-[3-(piperidine-1-sulfonyl)-phenyl]-pyrimidine-2,4-diamineHCID 57675084—

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528143B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-5b1d387dc1a84ff9bde678d981ed6d76
출처 메모uspto-grants-2009_05