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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699953Generated: November 1, 2026

Hydrochloric Acid → HCID 11005397, compound

https://huagongshe.com/reaction/1699953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant1-PentanesulfonamideHCID 10920696—
ReactantHCID 11100229HCID 11100229—
SolventDimethylformamideHCID 6228—
ProductHCID 11005397HCID 1100539753.5%

Reaction Steps

3-(3,4-Dichlorobenzyl)-2-methylbenzo[b]thiophene-5-carboxylic acid (160 mg) was dissolved in dry dimethylformamide (2 ml). Carbonyl-diimidazole (111 mg) was added and the mixture was stirred at room temperature for 1 hr. To the reaction mixture were added n-pentanesulfonamide (108 mg) and 1,8-diazabicyclo[5,4,0]undec-7-ene (122 mg) and the mixture was stirred at 100° C. for 1.5 hr. The reaction mixture was cooled in ice, and the pH thereof was adjusted to pH 4 with 1N hydrochloric acid. The mixture was partitioned between ethyl acetate and water. The organic layer was washed twice with water, dried over magnesium sulfate and concentrated to dryness under reduced pressure. The residue was eluted by silica gel column chromatography (hexane:ethyl acetate=1:1) . The resulting residue was crystallized from hexane-ethyl acetate to give 3-(3,4-dichlorobenzyl)-2-methyl-5-(n-pentanesulfonylcarbamoyl)benzo[b]thiophene (118 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06348474B1
Source datasetuspto-grants-2002_02
ORD IDord-7f625d11673a4f00a6847b4ed5f34dba
Source noteuspto-grants-2002_02