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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46717생성일: 2026년 10월 24일

Formaldehyde → Rifampicin

https://huagongshe.com/ko/reaction/46717

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물1,3,5-Trimethyl-1,3,5-triazacyclohexaneHCID 7952—
반응물1-Amino-4-methylpiperazineHCID 81349—
반응물RifamycinHCID 6324616—
반응물Rifamycin SHCID 6436726—
용매Acetic AcidHCID 176—
용매DimethylformamideHCID 6228—
생성물RifampicinHCID 135398735—

반응 단계

7 g. Rifamycin S are dissolved in 25 ml. dimethylformamide, then, while stirring, there are successively added 2.4 g. acetic acid, 0.6 g. paraformaldehyde and 0.85 g. 1,3,5-trimethyl-hexahydro-1,3,5-triazine. The mixture is then kept at 50° C. for 3 hours until the reaction is completed, with the formation of 3-methyl-1,3-oxazino (5,6-c) rifamycin (thin layer chromatography on silica gel 60 F254 - Merck: blue spot at Rf 0.19, eluent chloroform:methanol 9:1 v/v). 3.1 g. 1-amino-4-methylpiperazine are then added and the reaction is continued at 50° C. for about 1 hour until it is completed, as demonstrated by the disappearance of the blue spot in the TLC. After treatment in the usual way, a high yield (7.2 g.) of rifampicin is obtained. It can easily be purified by crystallisation from acetone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04174320
출처 데이터셋uspto-grants-1979_11
ORD IDord-720ad38bec7f46d0aac4239ff9d6ccb0
출처 메모uspto-grants-1979_11