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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425097Generated: November 1, 2026

2-Methylbenzoic acid → HCID 11541305, compound

https://huagongshe.com/reaction/2425097

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzoic acidHCID 8373—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant4-Chloro-6-methyl-10,10-dioxo-2-piperazin-1-yl-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cyclo heptene-8-carboxylic acid methyl esterHCID 11541072—
SolventDimethylformamideHCID 6228—
ProductHCID 11541305HCID 11541305—

Reaction Conditions

Temperature22 °C

Reaction Steps

Carbonyl diimidazole (0.074 g 0.55 mmol) was added to a solution of 2-toluic acid (0.111 g, 0.67 mmol) in DMF (3 mL) and stirred at 22° C. for 1 h. To this, a solution of 4-chloro-6-methyl-10,10-dioxo-2-piperazin-1-yl-10,11-dihydro-5-oxa-10lambda*6*-thia-dibenzo[a,d]cycloheptene-8-carboxylic acid methyl ester (free base of example 16, 0.2 g, 0.45 mmol) in DMF (2 mL) was added and stirred at 22° C. for 1 h. Solvent was removed and ice water (5 mL) was added. The solid separated was filtered, washed with water. The crude product obtained was purified by column chromatography (silica gel, ethyl acetate/pet ether) to obtain the title compound. Yield: 0.093 g (53%); mp: 201-204° C.; 1H NMR (DMSO-d6, 500 MHz): δ 2.23 (s, 3H, CH3), 2.64 (s, 3H, CH3), 3.15 (s, 2H, CH2), 3.28 (s, 2H, CH2), 3.34 (s, 2H, CH2), 3.39 (s, 2H, CH2), 3.87 (s, 3H, OCH3), 5.16 (s, 2H, CH2), 7.12 (s, 1H, Ar), 7.16 (s, 1H, Ar), 7.20 (m, 4H, Ar), 8.11 (s, 1H, Ar), 8.16 (s, 1H, Ar); MS: m/e (ES+) 555 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964631B2
Source datasetuspto-grants-2011_06
ORD IDord-b5c406d1237d4bddac64b2e7618e575b
Source noteuspto-grants-2011_06