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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 967775생성일: 2026년 10월 23일

4-(Methylamino)benzoic acid → UP9V9DB2RD

https://huagongshe.com/ko/reaction/967775

반응식

참여 물질

역할이름HCID투입량
반응물4-(Methylamino)benzoic acidHCID 66345—
반응물Sodium BicarbonateHCID 516892—
반응물1-[2-(4-Cyanophenyl)ethyl]piperidin-4-spiro-2'-oxiraneHCID 85819721—
촉매Scandium(III) triflateHCID 2734571—
용매WaterHCID 962—
용매AcetonitrileHCID 6342—
생성물UP9V9DB2RDHCID 1298648164.5%

반응 단계

Scandium trifluoromethanesulfonate (609 mg) was added to a mixture of the compound (500 mg) obtained in Step 3 of Example 1, 4-methylaminobenzoic acid (343 mg) and anhydrous acetonitrile (10 mL) under cooling with ice-water, and the mixture was stirred at room temperature for sixty eight hours under nitrogen atmosphere. Water (50 mL) and acetonitrile (10 mL) were added to the resulting mixture and the pH of the mixture was adjusted to above 9 with sodium hydrogen carbonate, insoluble matter was removed by filtration and the filtrate was concentrated under reduced pressure. Water in the residue was removed by azeotrope with ethanol, soluble components in the residue were dissolved in ethanol and the insoluble matter was removed by filtration. The filtrate was concentrated under reduced pressure and then, the residue was dissolved in water (50 mL) and the pH of the solution was adjusted to 7 by diluted hydrochloric acid. Precipitate was collected by filtration and washed with water and ethyl acetate successively under stirring. The precipitate was collected by filtration and dried to obtain the titled compound (524 mg) as powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06956046B2
출처 데이터셋uspto-grants-2005_10
ORD IDord-4299d678945a4105be6f8c2c05d2b8d2
출처 메모uspto-grants-2005_10