HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-(Phenazin-1-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-Aminophenazine | HCID 76138 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | N-(Phenazin-1-yl)acetamide | HCID 57896198 | — |
Reaction Steps
Scheme 8 provides a synthetic route to a 1-acetamido-N-ethyl phenazine derivative (35). A 3-amino-catechol hydrochloride (30) is reacted with silver oxide and anhydrous sodium sulfate in ethyl acetate to give 3-amino-1,2-quinone (31), which is further reacted in situ with ortho phenylenediamine (32) to give 1-amino phenazine (33). The amino phenazine (33) is acetylated with acetic anhydride in acetic acid to give 1-acetamido phenazine (34). The resulting 1-acetamido phenazine is reacted with diethyl sulfate in the presence of potassium carbonate to give N-ethyl-1-acetamido-phenazine (35)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08008037B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-be5d89319bb64e8d9503f094879855df |
| Source note | uspto-grants-2011_08 |