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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410155Generated: October 29, 2026

Hydrochloric Acid → HCID 46216064, compound

https://huagongshe.com/reaction/410155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantO-PhenylenediamineHCID 7243—
ReactantBenzenesulfonic AcidHCID 7371—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl orthoformateHCID 31214—
ReactantLithium diisopropylamideHCID 2724682—
ReactantEthyl 4-(3-(trifluoromethyl)pyridin-2-yloxy)benzoateHCID 59326875—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 46216064HCID 46216064—

Reaction Steps

A solution of benzene-1,2-diamine (175 mg, 1618 μmol), triethyl orthoformate (665 μL, 4353 μmol), and benzenesulfonic acid (10 mg, 65 μmol) in toluene (1.6 mL) was heated to reflux for 4 h and then slowly distilled to remove half of the solvent. The mixture was then cooled to RT and neutralized with diisopropyl amine, followed by addition of a solution of ethyl 4-(3-(trifluoromethyl)pyridin-2-yloxy)benzoate (554 mg, 1780 μmol) in 1.7 mL of THF. The mixture was cooled to −78° C. and 1.2 equiv of LDA (0.971 mL, 2.0M) was added. After aging at −78° C. for 1.5 h, the mixture was warmed to RT and stirred for 1.5 h and then 2N HCl was added and the mixture was agitated for 15 min. Following that, the mixture was adjusted to pH 9 with 1N NaOH. Ethyl acetate was added and the layers were separated, the aqueous was extracted with ethyl acetate (3×), and the combined organics were washed with brine, dried over Na2SO4, filtered and concentrated. Following purification, (1H-benzo[d]imidazol-2-yl)(4-(3-(trifluoromethyl)pyridin-2-yloxy)phenyl)methanone was obtained. MS (ESI, pos. ion) m/z: 384 (M+1). IC50 (uM) +++++.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759532B2
Source datasetuspto-grants-2014_06
ORD IDord-5dbed1a65bc24b8eb7ce41fdbd2c59e3
Source noteuspto-grants-2014_06