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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 889662생성일: 2026년 10월 25일

Methanesulfinyl chloride → Methanesulfinic acid (6-chloro-pyridin-3-yl methyl)-amide

https://huagongshe.com/reaction/889662

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfinyl chlorideHCID 548463—
반응물5-(Aminomethyl)-2-chloropyridineHCID 7020927—
용매TetrahydrofuranHCID 8028—
생성물Methanesulfinic acid (6-chloro-pyridin-3-yl methyl)-amideHCID 58545437—

반응 단계

Methanesulfinyl chloride was obtained as described in the literature. A solution of C-(6-chloro-pyridin-3-yl)-methylamine (2.1) (25 g, 178 mmol) in tetrahydrofuran (200 ml) was cooled to 0° C. and methanesulfinyl chloride (7 g, 71 mmol) was added dropwise. The solution was allowed to warm to room temperature and stirred for 16 hours. The precipitate was removed by filtration, the filtrate was diluted with EtOAc and washed with H2O. The organic phase was dried over Na2SO4 and evaporated under reduced pressure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08252939B2
출처 데이터셋uspto-grants-2012_08
ORD IDord-3be19a7127c34e83a55bdf5cf018e576
출처 메모uspto-grants-2012_08