HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ammonium Acetate → HCID 59341838, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ammonium Acetate | HCID 517165 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | 1-(1-(Quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl)ethanone | HCID 59341802 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | HCID 59341838 | HCID 59341838 | — |
| Produkt | HCID 59341949 | HCID 59341949 | — |
Reaktionsschritte
To a solution of 1-(3-quinolin-6-ylmethyl-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl)-ethanone (150 mg, 0.493 mmol) in MeOH (5 mL) was added ammonium acetate (76 mg, 0.987 mmol). The reaction was stirred for 2 hours at room temperature. Sodium cyano borohydride (62 mg, 0.987) was added and the reaction was heated to 70° C. for 16 hours. LC-MS showed ˜1:1 ratio of alcohol and amine. The reaction was concentrated and purified by a reverse-phase C-18 preparative HPLC eluting with ACN—H2O having 0.1% acetic acid to give 1-(3-quinolin-6-ylmethyl-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl)-ethanol (70 mg) and 1-(3-quinolin-6-ylmethyl-3H-[1,2,3]triazolo[4,5-b]pyrazin-5-yl)-ethylamine (20 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07732604B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-ee9a8ec357bc4d9d80f60139cabbd464 |
| Quellennotiz | uspto-grants-2010_06 |