HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminoadamantan-1-ol → 4-{2-[3-(5-Hydroxy-adamantan-2-ylcarbamoyl)-phenoxy]-ethyl}-piperidine-1-carboxylic acid isopropylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminoadamantan-1-ol | HCID 2857447 | — |
| Reactant | 3-[2-(1-Isopropylcarbamoyl-piperidin-4-yl)ethoxy]-benzoic acid | HCID 66929710 | — |
| Product | 4-{2-[3-(5-Hydroxy-adamantan-2-ylcarbamoyl)-phenoxy]-ethyl}-piperidine-1-carboxylic acid isopropylamide | HCID 25242327 | — |
Reaction Steps
Prepared from 3-[2-(1-isopropylcarbamoyl-piperidin-4-yl)-ethoxy]-benzoic acid and 4-amino-1-hydroxyadamantane. 1H NMR (400 MHz, CDCl3): δ 7.31-7.37 (m, 2H), 7.23-7.26 (m, 1H), 7.04 (dd, 1H), 6.37 (d, 1H), 4.18-4.24 (m, 1H), 4.06 (t, 2H), 3.98 (septet, 1H), 3.90 (d, 2H), 2.82 (t, 2H), 2.17-2.29 (m, 3H), 1.92-1.99 (m, 2H), 1.73-1.86 (m, 11H), 1.59 (d, 2H), 1.19-1.30 (m, 2H), 1.16 (d, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809540B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-1679bf488baf45bc89e443ed1a020658 |
| Source note | uspto-grants-2014_08 |