HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
6-Methylpyridine-2-carboxylic acid → Methyl 3-[[(6-methyl-2-pyridinyl)carbonyl]amino]tricyclo[3.3.1.13,7]decane-1-carboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 6-Methylpyridine-2-carboxylic acid | HCID 70282 | — |
| Edukt | Methyl 3-aminoadamantane-1-carboxylate hydrochloride | HCID 2852886 | — |
| Edukt | 6-Methyl-pyridine-2-carboxylic acid (3-amino-adamantan-yl)-amide | HCID 58358605 | — |
| Produkt | Methyl 3-[[(6-methyl-2-pyridinyl)carbonyl]amino]tricyclo[3.3.1.13,7]decane-1-carboxylate | HCID 67083637 | 75% |
Reaktionsschritte
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%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07947680B2 |
| Quelldatensatz | uspto-grants-2011_05 |
| ORD ID | ord-0107d6f9fdda4987b260d0acfc3ecaac |
| Quellennotiz | uspto-grants-2011_05 |