돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2107334생성일: 2026년 10월 26일

m-Chloroperbenzoic acid → 2-[2-(Isobutylamino)benzylsulfinyl]imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/2107334

반응식

참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물Sodium BicarbonateHCID 516892—
반응물2-[2-(Isobutylamino)benzylthio]imidazo[4,5-b]pyridineHCID 14839437—
용매ChloroformHCID 6212—
생성물2-[2-(Isobutylamino)benzylsulfinyl]imidazo[4,5-b]pyridineHCID 14839438—

반응 단계

In 20 ml of chloroform was dissolved 900 mg of 2-[2-(isobutylamino)benzylthio]imidazo[4,5-b]pyridine. To the resulting solution was portionwise added under chilling with ice 618 mg of m-chloroperbenzoic acid (purity: 80%) over a period of 30 min. To the mixture was added a saturated NaHCO3 solution, and the resulting mixture was then stirred. The organic phase was separated and extracted successively with 20 ml of 0.1N NaOH and 10 ml of 0.1N NaOH. The alkaline extracts were combined and neutralized by NH4Cl, and the deposited oil was extracted with chloroform. The chloroform extract was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate and placed under reduced pressure to distill off the solvent. The residue was crystallized by addition of diethyl ether. The crystalline product was washed with diethyl ether to give 195 mg of 2-[2-(isobutylamino)benzylsulfinyl]imidazo[4,5-b]pyridine as a pale yellow crystalline powder. m.p.: 116° C. (decompn.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04933458
출처 데이터셋uspto-grants-1990_06
ORD IDord-c3c599e2d6d74f9aaa00d14dd2451530
출처 메모uspto-grants-1990_06