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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 5-Hydroxypyridine-2-carboxylic acid | HCID 268740 | — |
| 반응물 | ((S)-6-{[(4-methoxybenzyl)(tetrahydropyran-4-ylmethyl)amino]methyl}-1,2,3,4-tetrahydronaphthalen-2-yl)methylamine | HCID 66663221 | — |
| 반응물 | (S)-6-{[(4-Methoxybenzyl)(tetrahydropyran-4-ylmethyl)amino]methyl}-1,2,3,4-tetrahydronaphthalen-2-ylamine | HCID 66664086 | — |
| 생성물 | N-(4-Methoxybenzyl)-1-(tetrahydro-2H-pyran-4-yl)methanamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08841290B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-191f7116e62e45bf9699b09e7df12eaa |
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| 출처 메모 | uspto-grants-2014_09 |
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