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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112705Generated: October 30, 2026

Acetic Anhydride → (E)-3-[6-(acetylamino)pyridin-3-yl]-N-methyl-N-(3-methyl-1H-inden-2-ylmethyl)acrylamide

https://huagongshe.com/reaction/2112705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium BicarbonateHCID 516892—
Reactant(E)-3-[6-aminopyridin-3-yl]-N-methyl-N-(3-methyl-1H-inden-2-ylmethyl)acrylamideHCID 22593796—
SolventTetrahydrofuranHCID 8028—
Product(E)-3-[6-(acetylamino)pyridin-3-yl]-N-methyl-N-(3-methyl-1H-inden-2-ylmethyl)acrylamideHCID 9799030249%

Reaction Steps

To a solution of (E)-3-[6-aminopyridin-3-yl]-N-methyl-N-(3-methyl-1H-inden-2-ylmethyl)acrylamide (0.159 g, 0.5 mmole), from Example 26, in anhydrous THF (20 mL) was added NaHCO3 (0.126 g, 1.5 mmole) followed by acetic anhydride (0.153 g, 0.15 mmole). The mixture was heated at reflux for 40 hr, then was concentrated under vacuum. The residue was partitioned between H2O and EtOAc, and the organic layer was dried over MgSO4, filtered and concentrated. The residue was triturated with diethyl ether to give the title compound (0.135 g, 74.8%) as an off-white solid: MS (ES) m/e 3623 (M+H)+. Anal. Calcd for C22H23N3O2.0.25H2O: C, 72.20; H, 6.47; N, 11.47. Found: C, 72.42; H, 6.45; N, 11.07.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524843B2
Source datasetuspto-grants-2009_04
ORD IDord-1adcee913cb7492e893c073f440e04ae
Source noteuspto-grants-2009_04