Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | HCID 54573576 | HCID 54573576 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 22839713 | HCID 22839713 | — |
Reaction Steps
To a stirred solution of 6α-amino androsta-1,4-diene-3,17-dione (1,4 g) in 5.5 ml of dry pyridine, 2.8 ml of acetic anhydride are added dropwise at room temperature. The solution is stirred for 90 minutes and then water is dropped into the cooled (0° C.) solution. After 10 minutes stirring the reaction mixture is extracted with five 100 ml portions of ethyl acetate which are collected and dried over anhydrous sodium sulphate. The solvent is then removed in vacuum to yield a crude which is purified by chromatography on silica gel so obtaining 1.30 g of pure 6α-acetylamino androsta-1,4-diene-3,17-dione;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04771043 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-a000c901c8834d5e93e85d8f2c62be34 |
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| Source note | uspto-grants-1988_09 |
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