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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1388496생성일: 2026년 10월 27일

Acrylamide → Rifamycin

https://huagongshe.com/reaction/1388496

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참여 물질

역할이름HCID투입량
반응물AcrylamideHCID 6579—
반응물[(9E,19E,21Z)-2,15,17,29-tetrahydroxy-27-[2-(4-iodoanilino)-2-oxoethoxy]-11-methoxy-3,7,12,14,16,18,22-heptamethyl-6,23-dioxo-8,30-dioxa-24-azatetracyclo[23.3.1.14,7.05,28]triaconta-1(29),2,4,9,19,21,25,27-octaen-13-yl] acetateHCID 6507126—
생성물RifamycinHCID 632461693.8%

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온도4 °C

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Fifty grams (wet weight) of acrylamide gel entrapped cell of Monocillium spp. (ATCC 20621), prepared through the procedures described in Example 4, were added to 2 l of centrifuged rifamycin B fermentation broth (6100 mgr rifamycin B/l). After reaction at 45° C. for 25 hours were aeration and agitation, the immobilized enzyme pellets were recovered through filtration on a sintered glass. It was extensively washed with 500 ml of acetone. The residual precipitates were completely solubilized by addition of another 500 ml of acetone. Thereto, 100 ml of ascrobic acid solution (10% in water) were added dropwisely while gently stirring. After confirming complete reduction to rifamycin SV, the pH was adjusted to 3.5 and the acetone was removed by evaporation with suction at 40° C. The solution was chilled to 4° C. for one day and the yellowish precipitate thus formed was recovered through filtration and dried. By this procedure, 12.5 gr of crude rifamycin SV were obtained (Purity=84%, Yield=93.8%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04431735
출처 데이터셋uspto-grants-1984_02
ORD IDord-972b87b4d1d2466cacb0213ed8c15cde
출처 메모uspto-grants-1984_02