HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid → HCID 67165427, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-((tert-Butoxycarbonyl)amino)cyclopentanecarboxylic acid | HCID 3564732 | — |
| Edukt | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Edukt | 6-Chloro-7-methoxy-9h-pyrido[3,4-b]indol-8-amine | HCID 21362743 | — |
| Produkt | HCID 67165427 | HCID 67165427 | — |
Reaktionsschritte
6-chloro-7-methoxy-9H-β-carboline-8-ylamine and 2-tert-butoxycarbonylamino-cyclopentanecarboxylic acid were reacted using Method A. To this product was added 5 ml of 4N HCl/dioxane and the resulting mixture was allowed to stir at RT. The reaction was followed by LC-MS until completion. Evaporation was allowed to remove all the solvent which gave a crude HCl salt. The desired product was then purified by preparative HPLC. 1H-NMR (300 MHz, DMSO-d6): δ 1.68 (m, 1H), 1.84 (m, 2H), 2.06 (m, 2H), 2.20 (m, 1H), 3.46 (m, 1H), 3.67 (m, 1H), 3.89 (s, 3H), 8.24 (d, 2H), 8.61 (d, 1H), 8.72 (s, 1H), 8.78 (d, 1H), 9.19 (s, 1H), 10.58 (s, 1H), 13.20 (s, 1H). Retention Time (LC, method: ammonium acetate standard): 1.54 min. MS (M+H+): 359.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07951801B2 |
| Quelldatensatz | uspto-grants-2011_05 |
| ORD ID | ord-f5cc0a10dfd448c08fd8e99ce2ea5bb7 |
| Quellennotiz | uspto-grants-2011_05 |