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C2HF3O2*C24H29N3O8
(4S,4aS,5aR,12aS)-4-dimethylamino-3,10,12,12a-tetrahydroxy-7-[(methoxy(methyl)amino)-methyl]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide mono hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In methanol |
(4S,4aS,5aR,12aS)-4-dimethylamino-3,10,12,12a-tetrahydroxy-7-[(methoxy(methyl)amino)-methyl]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide
(4S,4aS,5aR,12aS)-4-dimethylamino-3,10,12,12a-tetrahydroxy-7-[(methoxy(methyl)amino)-methyl]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide mono hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In ethanol; water at 5℃; pH=1.3 - 1.6; | |
With hydrogenchloride In ethanol pH=1.3 - 1.6; |
7-formylsancycline
(4S,4aS,5aR,12aS)-4-dimethylamino-3,10,12,12a-tetrahydroxy-7-[(methoxy(methyl)amino)-methyl]-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydro-naphthacene-2-carboxylic acid amide mono hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: sodium cyanoborohydride / N,N-dimethyl acetamide / 0.25 h / 20 °C / Inert atmosphere 2: hydrogenchloride / ethanol; water / 5 °C / pH 1.3 - 1.6 View Scheme |
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