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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351776Generated: October 25, 2026

Chlorotriethylsilane → HCID 22714347, compound

https://huagongshe.com/reaction/351776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotriethylsilaneHCID 13819—
ReactantN,N-Dimethyl-1H-imidazole-1-sulfonamideHCID 395751—
ReactantHCID 22714346HCID 22714346—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22714347HCID 22714347100%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Butyllithium (30.1 ml) was added slowly at −78° C. to a solution of N,N-dimethyl-1H-imidazol-1-sulfonamide (8,4 g) in tetrahydrofuran (150 ml) and the mixture was stirred at −78° C. for 15 minutes. Chlorotriethylsilane (8.1 ml) was added and the mixture was stirred till the temperature reached 20° C. The mixture was cooled till −78° C., butyllithium (30.1 ml) was added, the mixture was stirred at −78° C. for 1 hour and allowed to reach −15° C. The mixture was cooled again till −78° C., a solution of 6-(4-chlorobenzoyl)-1-methyl-4-phenyl-2(1H)-quinolinone (15 g) in tetrahydrofuran (30 ml) was added and the mixture was stirred till the temperature reached 20° C. The mixture was hydrolized and extracted with ethyl acetate. The organic layer was dried, filtered off and evaporated till dryness. The product was used without further purification, yielding 26 g (100%) of (±)-4-[(4-chlorophenyl)(1,2-dihydro-1-methyl-2-oxo-4-phenyl-6-quinolinyl)hydroxymethyl]-N,N-dimethyl-2-(triethylsilyl)-1H-imidazole-1-sulfonamide (interm. 3-a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743805B2
Source datasetuspto-grants-2004_06
ORD IDord-e6fc411faa16427690fdf219e21c4fae
Source noteuspto-grants-2004_06