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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1988413생성일: 2026년 10월 26일

Cyclohexanemethylamine → 4-(2-(cyclohexylmethylamino)benzo[d]oxazol-6-yloxy)-N-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/1988413

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanemethylamineHCID 76688—
반응물N-methyl-4-(2-(methylsulfinyl)benzo[d]oxazol-6-yloxy)picolinamideHCID 57725414—
용매TetrahydrofuranHCID 8028—
생성물4-(2-(cyclohexylmethylamino)benzo[d]oxazol-6-yloxy)-N-methylpyridine-2-carboxamideHCID 57725559—

반응 단계

To a solution of 4-(2-(methylsulfinyl)benzo[d]oxazol-6-yloxy)-N-methylpyridine-2-carboxamide (1.40 g, 4.23 mmol, 1.0 eq) in 15 mL of THF was added cyclohexylmethanamine (955 mg, 8.46 mmol, 2.0 eq) at room temperature. The reaction mixture was stirred at that temperature for 2 hours. After the solvent was removed under reduced pressure, the residue was dissolved in 150 mL of ethyl acetate. The resulting mixture was washed with water (20 mL), brine (20 mL), then dried over MgSO4, filtered, and evaporated under reduced pressure to give crude product, which was purified by silica gel column eluted with ethyl acetate and hexane to give the titled compound. MH+=381.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07553854B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-e4b7d7ce443b4d039b1d1f65a7e07c3c
출처 메모uspto-grants-2009_06