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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77419생성일: 2026년 10월 25일

5-Hydroxypyridine-2-carboxylic acid → N-(4-Methoxybenzyl)-1-(tetrahydro-2H-pyran-4-yl)methanamine

https://huagongshe.com/reaction/77419

반응식

참여 물질

역할이름HCID투입량
반응물5-Hydroxypyridine-2-carboxylic acidHCID 268740—
반응물((S)-6-{[(4-methoxybenzyl)(tetrahydropyran-4-ylmethyl)amino]methyl}-1,2,3,4-tetrahydronaphthalen-2-yl)methylamineHCID 66663221—
반응물(S)-6-{[(4-Methoxybenzyl)(tetrahydropyran-4-ylmethyl)amino]methyl}-1,2,3,4-tetrahydronaphthalen-2-ylamineHCID 66664086—
생성물N-(4-Methoxybenzyl)-1-(tetrahydro-2H-pyran-4-yl)methanamineHCID 55211610—

반응 단계

In Table 2, compounds which were prepared by reacting the appropriate acids with ((S)-6-{[(4-methoxybenzyl)(tetrahydropyran-4-ylmethyl)amino]methyl}-1,2,3,4-tetrahydronaphthalen-2-yl)methylamine or, correspondingly, (S)-6-{[(4-methoxybenzyl)(tetrahydropyran-4-ylmethyl)-amino]methyl}-1,2,3,4-tetrahydronaphthalen-2-ylamine according to method G and subsequent detachment of the 4-methoxybenzyl group according to method F are compiled. To prepare examples 2-06, 2-07 and 2-08, ((S)-6-{[(4-methoxybenzyl)(tetrahydropyran-4-ylmethyl)-amino]methyl}-1,2,3,4-tetrahydronaphthalen-2-yl)methylamine was reacted according to method G with 5-hydroxypyridine-2-carboxylic acid, the resulting amide was alkylated according to method D with the appropriate alkyl bromides on the phenolic hydroxyl group, and, finally, the 4-methoxybenzyl group was removed according to method F.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841290B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-191f7116e62e45bf9699b09e7df12eaa
출처 메모uspto-grants-2014_09