Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2057635Generated: October 26, 2026

Pyridine → Acetic Anhydride

https://huagongshe.com/reaction/2057635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantN-(3-Methylphenyl)anilineHCID 14569—
Reactant2-Pyridinecarboxylic acid, 3-[(1-ethyl-2-methyl-1H-indol-3-yl)carbonyl]-HCID 109082—
Reactant3-Pyridinecarboxylic acid, 2-((1-ethyl-2-methyl-1H-indol-3-yl)carbonyl)-HCID 112344—
SolventTolueneHCID 1140—
ProductAcetic AnhydrideHCID 7918—
ProductHCID 70544473HCID 70544473—

Reaction Steps

Following a procedure similar to that described in Example 3 but employing 1.6 g. of an isomer mixture comprising 2-[(1-ethyl-2-methyl-3-indolyl)carbonyl]-3-pyridinecarboxylic acid and 3-[(1-ethyl-2-methyl-3-indolyl)carbonyl]-2-pyridinecarboxylic acid, 0.95 g. of N-phenyl-m-toluidine, 0.5 ml. of pyridine and 6 ml. of acetic anhydride there was obtained 7-(1-ethyl-2-methyl-3-indolyl)-7-(m-tolylphenylamino)furo[3,4-b]pyridine-5(7H)-one as a yellow solid, m.p. 178°-190° C. (dec.) A toluene solution of the product contacted with acidic clay or phenolic resin developed an orange image.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04211872
Source datasetuspto-grants-1980_07
ORD IDord-aa045abb4cd845ea89b33ef4654458d8
Source noteuspto-grants-1980_07