HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Benzyl chloroformate → Ethyl-2-benzyloxycarbonyloxyamino-4-methyl-thiazole-5-carboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Benzyl chloroformate | HCID 10387 | — |
| Edukt | Ethyl 2-amino-4-methylthiazole-5-carboxylate | HCID 343747 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Ethyl-2-benzyloxycarbonyloxyamino-4-methyl-thiazole-5-carboxylate | HCID 21911467 | 48% |
Reaktionsschritte
A 3 M aq. NaHCO3 solution (10 mL, 30 mmol) was added to a stirred solution of ethyl-2-amino-4-methyl-thiazole-5-carboxylate (372 mg, 2 mmol) in THF (20 mL) at 0–5° C. Benzyl chloroformate (500 μL) was added. After 2 h, additional benzyl chloroformate (500 μL) and the biphasic solution was stirred for an additional 2 h at 0–5° C. The mixture was diluted with dichloromethane (50 mL) and water (30 mL). The organic layer was separated, dried (MgSO4), filtered and concentrated. The residue was chromatographed on a silica gel column. Elution with 10% EtOAc in hexanes followed by 20% and 30% EtOAc in hexanes afforded the title compound (310 mg, 48%) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07091223B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-f75c4e99532d4a508cd22f8965bec48f |
| Quellennotiz | uspto-grants-2006_08 |