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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393860Generated: November 1, 2026

Imidazole → HCID 59680503, compound

https://huagongshe.com/reaction/1393860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium hydrideHCID 24758—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantXanthane hydrideHCID 2735329—
ReactantAmmonium chloride monohydrateHCID 57429219—
ReactantHCID 69310221HCID 69310221—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59680503HCID 5968050320%

Reaction Conditions

Temperature0 °C

Reaction Steps

2,2-Bis{4-[(4-fluorobenzyl)oxy]phenyl}acetic acid (1.00 g, 2.17 mmol) was dissolved in tetrahydrofuran (7 ml), and 1,1′-carbonyldiimidazole (0.423 g, 2.61 mmol) was added thereto. The imidazole mixture was stirred for 1 hour at room temperature. Sodium hydride (60% oil suspension 0.087 g, 2.17 mmol) was suspended in tetrahydrofuran (7 ml), and 3-amino-1,2,4-dithiazole-5-thione (0.326 g, 2.17 mmol) was added thereto. After being stirred for 30 minutes at 0° C., the reaction mixture, with the imidazole mixture added thereto, was stirred for 17 hours at room temperature. The reaction mixture, with saturated ammonium chloride water added thereto, was extracted with ethyl acetate. The organic layer was washed with saturated sodium bicarbonate water and saturated brine successively, dried over MgSO4, and then concentrated. The obtained residue was purified by silica gel column chromatography (chloroform), to give 2,2-bis{4-[(4-fluorobenzyl)oxy]phenyl}-N-(3-thioxo-3H-1,2,4-dithiazol-5-yl)acetoamide (Compound 11) (0.256 g, 20%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348017B2
Source datasetuspto-grants-2008_03
ORD IDord-c63439127a974ef782178709cf197f82
Source noteuspto-grants-2008_03