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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2173738생성일: 2026년 10월 25일

Ethanol → Caspofungin Acetate

https://huagongshe.com/reaction/2173738

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참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물L-TyrosineHCID 6057—
반응물Ethyl AcetateHCID 8857—
반응물n-{(2r,6s,9s,11r,12s,14As,15s,20s,23s,25as)-12-[(2-aminoethyl)amino]-20-[(1r)-3-amino-1-hydroxypropyl]-23-[(1s,2s)-1,2-dihydroxy-2-(4-hydroxyphenyl)ethyl]-2,11,15-trihydroxy-6-[(1r)-1-hydroxyethyl]-5,8,14,19,22,25-hexaoxotetracosahydro-1h-dipyrrolo[2,1-c:2',1'-l][1,4,7,10,13,16]hexaazacyclohenicosin-9-yl}-10,12-dimethyltetradecanamideHCID 2826718—
용매Acetic AcidHCID 176—
용매Methan(2H)olHCID 123113—
생성물Caspofungin AcetateHCID 6850808—

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By means of NMR the contents of caspofungin, ethanol, ethyl acetate and acetic acid were determined in the crystals obtained above as follows. Approximately 15 mg of sample and standard (DMB) were accurately weighed in a suitable vial. The samples were dissolved in MeOD by vortexing. The samples were measured at 600 MHz using a delay of 30 s at 300K. The spectra that were used for the calculation of the impurities in the aromatic region were measured using a delay of 5 s and 256 scans to enhance the signal to noise ratio. The analysis was carried out in duplo. Caspofungin was quantified using the tyrosine signal at 7.15 ppm. See Table 5 for results.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09056897B2
출처 데이터셋uspto-grants-2015_06
ORD IDord-e39fd8ca65ae4faeabc33b9378de8bba
출처 메모uspto-grants-2015_06