16α-Methyl-11-oxo Prednisolone
- Product Name
- 16α-Methyl-11-oxo Prednisolone
- CAS No.
- 2036-77-3
- Chemical Name
- 16α-Methyl-11-oxo Prednisolone
- Synonyms
- DMS-0;Dexamethasone imp J;Carbamazepine Impurity 26;(8S,9S,10R,13S,14S,16R,17R);Dexamethasone EP Impurity J;16α-Methyl-11-oxo Prednisolone;16Alpha-Methyl-11-oxo Prednisolone;Tobramycin and dexamethasone impurity J;Dexamethasone impurity 4/Dexamethasone EP Impurity J;Dexamethasone Impurity 10(Dexamethasone EP Impurity J)
- CBNumber
- CB22544463
- Molecular Formula
- C22H28O5
- Formula Weight
- 372.45
- MOL File
- 2036-77-3.mol
16α-Methyl-11-oxo Prednisolone Property
- Melting point:
- 197-199°C
- Boiling point:
- 574.4±50.0 °C(Predicted)
- Density
- 1.28±0.1 g/cm3(Predicted)
- storage temp.
- Refrigerator
- solubility
- Acetone (Slightly), Chloroform (Slightly), Methanol (Slightly)
- form
- Solid
- pka
- 12.38±0.70(Predicted)
- color
- White to Off-White
- Major Application
- pharmaceutical small molecule
N-Bromosuccinimide Price
- Product number
- M295350
- Product name
- 16α-Methyl-11-oxoPrednisolone
- Packaging
- 25mg
- Price
- $850
- Updated
- 2021/12/16
- Product number
- SHG0005877
- Product name
- 16-ALPHA-METHYL-11-OXO PREDNISOLONE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $496.54
- Updated
- 2021/12/16
16α-Methyl-11-oxo Prednisolone Chemical Properties,Usage,Production
Uses
A 16α-substituted Prednisolone as potent topical antiinflammatory agent.
Synthesis
1) Add 5.0 g of pregnane-1,4,16-triene-3,11,20-trione (compound (I-1)) with 0.02 times copper bromide dimethyl sulfide, 1.2 times trimethylchlorosilane, 2 times hexamethylphosphorotriamine to 60 ml of tetrahydrofuran, and slowly add 1.2 times methylmagnesium bromide dissolved in the tetrahydrofuran to carry out the Grignard reaction, the temperature of the reaction is -30??-20??. The reaction was protected by passing N2, and at the end of the reaction it was diluted with water, separated and dried to obtain the Grignard product (compound (II-1)); 2) React the above Grignard with 3 times potassium bicarbonate and 1.5 times m-chloroperoxybenzoic acid in dichloromethane at a reaction temperature of -30 to -25??C, and react until complete. The solution pH was adjusted to 1 with hydrochloric acid, concentrated under reduced pressure, cooled, separated and dried to obtain the compound dexamethasone EP impurity J(III-1), total yield 78.2%.
16α-Methyl-11-oxo Prednisolone Preparation Products And Raw materials
Raw materials
Preparation Products
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