HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methanol → HCID 22672527, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 2-Cyanoethyl N,N-diisopropylchlorophosphoramidite | HCID 2734844 | — |
| Edukt | 8-(3-Hydroxypropyl)-7-oxophenoxazin-3-yl 2,2-dimethylpropanoate | HCID 22672525 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | HCID 22672527 | HCID 22672527 | — |
Reaktionsschritte
36b (0.38 g, 1.1 mmol) was dissolved in 6 mL of anhydrous CH2Cl2. Triethylamine (1.5 mL) was added followed by 2-cyanoethyl diisopropylchlorophosphoramidite (0.29 mL, 1.3 mmol). The solution was kept at room temperature for 30 min, MeOH (0.1 mL) was added and the reaction was concentrated under vacuum. The residue obtained was partitioned between ethyl acetate and NaHCO3. The organic phase was washed with saturated NaCl, dried over Na2SO4 and concentrated to afford the crude amidite. It was dissolved in 2 mL of ether and added dropwise to ˜50 mL of hexane. The resultant orange solid was collected by filtration, washed with hexane and dried. The yield was 0.4 g.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06699975B2 |
| Quelldatensatz | uspto-grants-2004_03 |
| ORD ID | ord-12f83a610c1f470193d59c21eab882af |
| Quellennotiz | uspto-grants-2004_03 |