Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
6-Methylpyridine-2-carboxylic acid → Methyl 3-[[(6-methyl-2-pyridinyl)carbonyl]amino]tricyclo[3.3.1.13,7]decane-1-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 6-Methylpyridine-2-carboxylic acid | HCID 70282 | — |
| 반응물 | Methyl 3-aminoadamantane-1-carboxylate hydrochloride | HCID 2852886 | — |
| 반응물 | 6-Methyl-pyridine-2-carboxylic acid (3-amino-adamantan-yl)-amide | HCID 58358605 | — |
| 생성물 | Methyl 3-[[(6-methyl-2-pyridinyl)carbonyl]amino]tricyclo[3.3.1.13,7]decane-1-carboxylate | HCID 67083637 | 75% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08198275B2 |
| 출처 데이터셋 | uspto-grants-2012_06 |
| ORD ID | ord-abff979b194947d49952cd09f9327ab8 |
| 출처 메모 | uspto-grants-2012_06 |