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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703155Generated: October 29, 2026

Sodium Methoxide → 2-[(4-methoxy-3-methylpyridin-2-yl)methylsulfanyl]-5,5,7,7-tetramethyl-3H-cyclopenta[f]benzimidazol-6-one

https://huagongshe.com/reaction/703155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant5,7-dihydro-5,5,7,7-tetramethyl-2-[[(3-methyl-4-nitro-2-pyridyl)methyl]thio]indeno[5,6-d]imidazol-6(1H)-oneHCID 22151439—
SolventMethanolHCID 887—
Product2-[(4-methoxy-3-methylpyridin-2-yl)methylsulfanyl]-5,5,7,7-tetramethyl-3H-cyclopenta[f]benzimidazol-6-oneHCID 9865473—

Reaction Steps

A solution of 4.4 g of 5,7-dihydro-5,5,7,7-tetramethyl-2-[[(3-methyl-4-nitro-2-pyridyl)met hyl]thio]indeno[5,6-d]imidazol-6(lH)-one in 100 ml of absolute methanol was treated with 3 g of sodium methylate, whereupon the mixture was boiled at reflux for 18 hours under argon. After concentrating the reaction mixture in vacuo the residue was treated with methylene chloride whereupon the mixture was buffered by means of glacial acetic acid; the methylene chloride phase was extracted several times with a sodium bicarbonate solution, dried and evaporated. By recrystallisation from ethyl acetate there was obtained 5,7-dihydro-2-[[(4-methoxy-3-methyl-2-pyridyl)methyl]thio]-5,5,7,7-tetramethylindeno[5,6-d ]imidazol-6(lH)-one of melting point 222-226°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04981861
Source datasetuspto-grants-1991_01
ORD IDord-922ccdb4b814429cafddab210f39e175
Source noteuspto-grants-1991_01