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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251058생성일: 2026년 10월 25일

Pyridine, 3-chloro-, 1-oxide → 3-Piperidin-1-ylpyridine 1-oxide

https://huagongshe.com/reaction/251058

반응식

참여 물질

역할이름HCID투입량
반응물Pyridine, 3-chloro-, 1-oxideHCID 123133—
용매PiperidineHCID 8082—
생성물3-Piperidin-1-ylpyridine 1-oxideHCID 817408133.4%

반응 단계

A solution of 3-chloro-pyridine 1-oxide (2.40 g, 18.5 mmol) in piperidine (6 mL) was heated at 140° C. for 2 days. After the reaction mixture was cooled to room temperature the amine was removed, and the residue was purified by flash chromatography on a silica gel column (6:1 EtOAc/MeOH), affording 3,4,5,6-tetrahydro-2H-[1,3′]bipyridinyl 1′-oxide as a pale yellow solid (2.20 g, 67%). 1H NMR (CDCl3) δ 1.59-1.67 (m, 6H), 3.14-3.18 (m, 4H), 6.78 (dd, 1H, J=2.1, 8.7 Hz), 7.03 (dd, 1H, J=6.3, 8.7 Hz), 7.63-7.66 (m, 1H), 7.85-7.86 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863293B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-d733a3b63baf4b3a882717a762111948
출처 메모uspto-grants-2011_01