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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989212Generated: October 30, 2026

Chlorotrimethylsilane → HCID 21995562, compound

https://huagongshe.com/reaction/989212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant5-Methoxy-6-(trifluoromethyl)indolineHCID 11206713—
ReactantHCID 16792745HCID 16792745—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 21995562HCID 2199556260.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

A suspension of 3-(pyrid-3-ylaminosulphonyl)-aminobenzene (D39) (0.5 g, 2 mmol) in chloroform (40 ml) was treated with triethylamine (5 ml) and chlorotrimethylsilane (5 ml). The solution was evaporated to dryness, and the residue dissolved in dichloromethane (20 ml). Carbonyl diimidazole (0.32 g, 2 mmol) was added and after 1 h the reaction mixture was evaporated to dryness. Dimethylformamide (20 ml) and (5-methoxy-6-trifluoromethyl indoline (0.43 g, 2 mmol) was added, and the mixture heated to 100° C. for 2 h. The cooled solution was diluted with water (60 ml). Filtration and drying afforded a brown solid (0.6 g). Chromatography, eluting with 0-5% methanol in ethyl acetate afforded the product as a white solid (0.26 g, 26%), m.p.>215° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638953B2
Source datasetuspto-grants-2003_10
ORD IDord-fe0a7caa5f04410fb8b336afec7fa8c5
Source noteuspto-grants-2003_10