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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665008Generated: October 31, 2026

1,1'-Carbonyldiimidazole → HCID 67441840, compound

https://huagongshe.com/reaction/1665008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-Methanesulfonylbenzoic acidHCID 220380—
ReactantHCID 67440054HCID 67440054—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 67441840HCID 6744184075.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 3-methylsulfonylbenzoic acid (60 mg) in N,N-dimethylacetamide (1.3 mL) was added 1,1′-carbonyl-diimidazole (52 mg). The mixture was stirred at 50° C. for 20 min. After cooling to r.t., N-benzyl-N-hydrazinocarbonylmethyl-2-trifluoromethyl-benzenesulfonamide (100 mg) was added and the mixture was stirred at 100° C. overnight. After cooling to r.t. the mixture was diluted with ethyl acetate and washed with water. The organic phase was dried (MgSO4), filtered and concentrated under reduced pressure. The product was purified by chromatography (SiO2, dichloromethane to dichloromethane/methanol 95:5) to give N-benzyl-N-{2-[N′-(3-methanesulfonyl-benzoyl)-hydrazino]-2-oxo-ethyl}-2-trifluoromethyl-benzenesulfonamide (111 mg) as a colorless oil. MS: 570.3 ([M+H]+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039493B2
Source datasetuspto-grants-2011_10
ORD IDord-30adce3d434146e7814d169c75c995b7
Source noteuspto-grants-2011_10