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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550862생성일: 2026년 10월 25일

Tetrahydrofuran → 3-[(Pyridine-2-carbonyl)-amino]adamantane-1-carboxylic acid

https://huagongshe.com/reaction/550862

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물3-[(Pyridine-2-carbonyl)-amino]adamantane-1-carboxylic acid methyl esterHCID 49720449—
용매WaterHCID 962—
생성물3-[(Pyridine-2-carbonyl)-amino]adamantane-1-carboxylic acidHCID 2396198293.3%

반응 단계

To a round bottom flask was added 3-[(pyridine-2-carbonyl)-amino]-adamantane-1-carboxylic acid methyl ester (24.8 g, 78.9 mmol), tetrahydrofuran (250 mL), water (250 mL) and lithium hydroxide monohydrate (14.9 g, 355 mmol) and the mixture was stirred vigorously at room temperature for 25 hours. The crude mixture was concentrated under reduced pressure to remove most of the tetrahydrofuran, then the aqueous solution was diluted with water (200 mL) and the pH was adjusted to about 3-4 by adding solid citric acid monohydrate. A voluminous white precipitate appeared which was filtered, washed with water and dried under high vacuum at 50° C. to afford 22.1 g (93%) of the title compound, 3-[(pyridine-2-carbonyl)-amino]-adamantane-1-carboxylic acid, as a white solid. 1H NMR (400 MHz, CDCl3) δ 8.55-8.50 (m, 1H), 8.18 (d, J=7.7 Hz, 1H), 7.97 (br s, 1H), 7.85 (td, J=7.8, 1.8 Hz, 1H), 7.42 (ddd, J=7.6, 4.8, 1.3 Hz, 1H), 2.35-2.31 (m, 2H), 2.31-2.25 (m, 2H), 2.25-2.09 (m, 4H), 2.00-1.86 (m, 4H), 1.80-1.64 (m, 2H). ESI-MS m/z: 301.0 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947680B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-fb1848e28fc94686a0a6f0f597ac4571
출처 메모uspto-grants-2011_05