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CasNo: 2921-57-5
MF: C26H34O8
Synthesis |
Add 6L of dimethyl sulfoxide and 1kg of succinic anhydride in the reaction kettle, stir and dissolve at 25°C, add 0.8L of triethylamine, and stir for 10 minutes; add 1kg of methylprednisolone again, react at 30°C for 3 hours, add 10% hydrochloric acid water Terminate the reaction, separate 40 L of water, and stir for 30 minutes; filter and wash with water to obtain the crude product; the crude product is dissolved in 30 times of methanol temperature, and activated carbon is decolorized to obtain methylprednisolone succinate; the yield is 119%, and the content is 99.3%. |
InChI:InChI=1/C26H34O8/c1-14-10-16-17-7-9-26(33,20(29)13-34-22(32)5-4-21(30)31)25(17,3)12-19(28)23(16)24(2)8-6-15(27)11-18(14)24/h6,8,11,14,16-17,19,23,28,33H,4-5,7,9-10,12-13H2,1-3H3,(H,30,31)/t14-,16-,17-,19-,23+,24-,25-,26-/m0/s1
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Succinate esters, although frequently em...
6α-methylprednisolone 17-hemisuccinate
Methylprednisolone
6α-methylprednisolone-21-hydrogen succinate
Conditions | Yield |
---|---|
With
aq. buffer;
In
N,N-dimethyl-formamide;
at 25 ℃;
Rate constant;
Mechanism;
pH dependence;
|
6α-methylprednisolone 17-hemisuccinate
6α-methylprednisolone-21-hydrogen succinate
Conditions | Yield |
---|---|
In
water;
at 25 ℃;
Rate constant;
|
6α-methylprednisolone 17-hemisuccinate
6α-methylprednisolone 17-hemisuccinate
Methylprednisolone