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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30805생성일: 2026년 10월 24일

Diisopropylethylamine → N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamide

https://huagongshe.com/ko/reaction/30805

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-Methylpiperidine-4-carbonyl chlorideHCID 436503—
반응물2-Amino-4-chloropyridineHCID 581866—
용매DichloromethaneHCID 6344—
생성물N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamideHCID 69008397—

반응 조건

온도0 °C

반응 단계

A flask was flame dried and placed under a nitrogen atmosphere. 1-methylpiperidine-4-carbonyl chloride (1 eq) in anhydrous methylene chloride was added to the flask and brought to 0° C. To this was added the solution containing 4-chloropyridin-2-amine (1 eq), and diisopropylethylamine (5 eq) in anhydrous methylene chloride, which was stirred for 1 hour at 0° C. Reaction concentrated and partitioned between water and ethyl acetate. The organic layer was separated, washed with brine, dried over sodium sulfate and concentrated to give the crude product. Purification on silica gel, 10% methanol in methylene chloride to yield N-(4-chloropyridin-2-yl)-1-methylpiperidine-4-carboxamide as a slightly yellow crystal solid. HPLC=2.39 min; MS: MH+=254.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07423150B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-09769fb5fb4e43ffa1082f09d673b2a1
출처 메모uspto-grants-2008_09