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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1963698생성일: 2026년 10월 26일

Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → 1-methyl-N-(4-{[4-(methylamino)-3-nitrophenyl]oxy}pyridin-2-yl)piperidine-4-carboxamide

https://huagongshe.com/reaction/1963698

반응식

참여 물질

역할이름HCID투입량
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물1-Methylpiperidine-4-carboxylic acidHCID 2736939—
반응물[4-(2-Amino(4-pyridyloxy))-2-nitrophenyl]methylamineHCID 69006232—
용매DimethylformamideHCID 6228—
생성물1-methyl-N-(4-{[4-(methylamino)-3-nitrophenyl]oxy}pyridin-2-yl)piperidine-4-carboxamideHCID 69003266—

반응 단계

To a mixture of 1-methylpiperidine-4-carboxylic acid (1 eq) in N,N-dimethyl formamide and N,N-disopropylethylamine (4 eq) was added BOP (2 eq) and the mixture was stirred at ambient temperature until homogeneous. To it was added [4-(2-amino(4-pyridyloxy))-2-nitrophenyl]methylamine (1 eq) and the resulting mixture was stirred at 60° C. for 16 h. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was dried over sodium sulfate and the resulting 1-methyl-N-(4-{[4-(methylamino)-3-nitrophenyl]oxy}pyridin-2-yl)piperidine-4-carboxamide was purified by silica gel chromatography. MS: MH+=386.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08415382B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-e2dd8a0e441441d0b5cf868f4118c601
출처 메모uspto-grants-2013_04