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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 218015생성일: 2026년 10월 25일

6-Methylpyridine-2-carboxylic acid → Methyl 3-[[(6-methyl-2-pyridinyl)carbonyl]amino]tricyclo[3.3.1.13,7]decane-1-carboxylate

https://huagongshe.com/reaction/218015

반응식

참여 물질

역할이름HCID투입량
반응물6-Methylpyridine-2-carboxylic acidHCID 70282—
반응물Methyl 3-aminoadamantane-1-carboxylate hydrochlorideHCID 2852886—
반응물6-Methyl-pyridine-2-carboxylic acid (3-amino-adamantan-yl)-amideHCID 58358605—
생성물Methyl 3-[[(6-methyl-2-pyridinyl)carbonyl]amino]tricyclo[3.3.1.13,7]decane-1-carboxylateHCID 6708363775%

반응 단계

Intermediate 1 was also made via the same synthetic procedures for Intermediate 2 (see below). Starting from 3-amino-adamantane-1-carboxylic acid methyl ester hydrochloride (14.9 g, 60.8 mmol), coupling with 6-methyl-pyridine-2-carboxylic acid afforded 3-[(6-methyl-pyridine-2-carbonyl)-amino]-adamantane-1-carboxylic acid methyl ester (14.9 g, 75%). The methyl ester was then hydrolyzed to give 3-[(6-methyl-pyridine-2-carbonyl)-amino]-adamantane-1-carboxylic acid (12.2 g, 86%). Finally, the Curtius rearrangement of 3-[(6-methyl-pyridine-2-carbonyl)-amino]-adamantane-1-carboxylic acid (10.0 g, 31.8 mmol) yielded Intermediate 1 (8.48 g, 93%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08198275B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-abff979b194947d49952cd09f9327ab8
출처 메모uspto-grants-2012_06