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HRID 524981생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/524981

반응식

참여 물질

역할이름HCID투입량
반응물O-ToluidineHCID 7242—
반응물Sodium tartrate-2-hydrateHCID 517351—
반응물TrimethylaluminumHCID 16682925—
반응물methyl 1-(phenylsulfonyl)-3-(trifluoromethyl)-1H-pyrrole-2-carboxylateHCID 70922372—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물1-(Phenylsulfonyl)-N-o-tolyl-3-(trifluoromethyl)-1H-pyrrole-2-carboxamideHCID 70922319221.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09340547B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-b338121e6cbf435aa0d26dccff587f2e
출처 메모uspto-grants-2016_05