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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428996생성일: 2026년 10월 25일

m-Chloroperbenzoic acid → Catharanthine N-oxide

https://huagongshe.com/reaction/428996

반응식

참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물(+)-CatharanthineHCID 5458190—
용매DichloromethaneHCID 6344—
생성물Catharanthine N-oxideHCID 101458260—

반응 단계

To a solution of catharanthine (Formula III, 200 mg, 0.6 mmol) in dry methylene chloride (2 ml) at −20° C. under a positive atmosphere of argon was added m-chloroperbenzoic acid (132 mg, 0.8 mmol), and the mixture was stirred for 5 minutes. To the catharanthine N-oxide (IIIa; R═COOCH3; R1, R2, R3, and R4=H), thus formed was added a solution of vindoline (IV, 270 mg, 0.6 mmol) in methylene chloride (1 ml) and the mixture was cooled to −60° C. Trifluoroacetic anhydride (0.2 ml, 1.5 mmol) was added to the stirred reaction mixture maintained at −60° C. for 2 hours. After this time, the solvent and excess reagents were removed in vacuo at −20° C. to leave a reddish-brown residue containing the iminium intermediate. The intermediate was characterized by reverse phase high performance liquid chromatography (HPLC) (Waters Radial-Pak C18 or CN cartridge, methanol-H2O-Et3N as solvent system). It was shown that the yield of the iminium intermediate of Formula VI in this reaction exceeded 80%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE037449E1
출처 데이터셋uspto-grants-2001_11
ORD IDord-42d7c0a126df4261b7e95628824cc7d4
출처 메모uspto-grants-2001_11