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HRID 524981作成日:2026年10月27日

O-Toluidine → 1-(Phenylsulfonyl)-N-o-tolyl-3-(trifluoromethyl)-1H-pyrrole-2-carboxamide

https://huagongshe.com/reaction/524981

反応式

関与物質

役割名称HCID仕込み量
反応物O-ToluidineHCID 7242—
反応物Sodium tartrate-2-hydrateHCID 517351—
反応物TrimethylaluminumHCID 16682925—
反応物methyl 1-(phenylsulfonyl)-3-(trifluoromethyl)-1H-pyrrole-2-carboxylateHCID 70922372—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物1-(Phenylsulfonyl)-N-o-tolyl-3-(trifluoromethyl)-1H-pyrrole-2-carboxamideHCID 70922319221.2%

反応手順

In a three-necked round-bottom flask o-toluidine (0.53 g, 5 mmol) was dissolved in 15 mL of toluene under inert atmosphere. To this solution was added trimethy aluminium (2.5 mL, 5 mmol) and the mixture was stirred at room temperature during 10 minutes. Afterwards, a solution of methyl 1-(phenylsulfonyl)-3-(trifluoromethyl)-1H-pyrrole-2-carboxylate (207 mg, 0.62 mmol) in 15 mL of toluene were added and the reaction mixtures was heated at 80° C. over night. Next, the mixture was allowed to cool to room temperature and 2-3 mL of water were added to hydrolyze unreacted trimethyl aluminium and a 0,5M aqueous solution of disodium tartrate dihydrate were added stirring for a while. Afterwards, the two layers were separated and the aqueous phase was extracted with ethyl acetate. The organic mixture was washed with the same 0,5M aqueous solution of disodium tartrate dihydrate (25 mL), water and brine, dried and concentrated in vacuum to afford 560 mg of a residue that was used in the following step without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09340547B2
出典データセットuspto-grants-2016_05
ORD IDord-b338121e6cbf435aa0d26dccff587f2e
出典メモuspto-grants-2016_05