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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41806Generated: October 25, 2026

Acetic Anhydride → N-(Phenazin-1-yl)acetamide

https://huagongshe.com/reaction/41806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1-AminophenazineHCID 76138—
SolventAcetic AcidHCID 176—
ProductN-(Phenazin-1-yl)acetamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08535511B2
Source datasetuspto-grants-2013_09
ORD IDord-a44dffd78eeb485284484700dd580e32
Source noteuspto-grants-2013_09