HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Sulfate → 1-acetamido-N-ethyl phenazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(Phenazin-1-yl)acetamide | HCID 57896198 | — |
| Product | 1-acetamido-N-ethyl phenazine | HCID 67351462 | — |
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 | US08535511B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-c14dfd3622f64bb3ac2ebbc37bea83ac |
| Source note | uspto-grants-2013_09 |