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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 451412생성일: 2026년 10월 26일

Diisopropylethylamine → tert-butyl N-[1-(6-methylpyrimidin-4-yl)piperidin-4-yl]carbamate

https://huagongshe.com/reaction/451412

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Chloro-6-methylpyrimidineHCID 581796—
반응물4-Amino-1-Boc-piperidineHCID 1268291—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl N-[1-(6-methylpyrimidin-4-yl)piperidin-4-yl]carbamateHCID 67343276—

반응 조건

온도150 °C

반응 단계

A suspension of Boc-4-aminopiperidine (613 mg, 3 mmol), 4-chloro-6-methylpyrimidine (433 mg, 3.3 mmol) and N,N-diisopropylethyl amine (771 L, 4.5 mmol) in dioxane (12 mL) was heated to 150° C. in the microwave for 30 minutes. The reaction was diluted with water and extracted twice with ethyl acetate. The combined organic layers were washed with water, dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography on silica gel using a gradient from AcOEt to AcOEt/EtOH 9:1 as eluent. The title compound was obtained as a light yellow solid (693 mg, 79%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486967B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-6de883d95cf14582bc0237df04c0840d
출처 메모uspto-grants-2013_07