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药物详细合成路线

Name Dehydroepiandrosterone;Prasterone;PB-007;EL-10;DHEA;GL-701;Fidelin;Anastar;Prestara;Inflabloc;Aslera
Chemical Name 3beta-Hydroxyandrost-5-en-17-one
      Dehydroepiandrosterone
CAS 53-43-0
Related CAS
Formula C19H28O2
Structure
Formula Weight 288.43381
Stage 建议批准
Company Genelabs (Proprietary), Genelabs (Orphan Drug), Paladin (Orphan Drug), Jenapharm (Originator), Stanford University (Originator), Mipharm (Licensee), Pharmadigm (Licensee), Tanabe Seiyaku (Licensee), Watson (Licensee)
Activity/Mechanism Acute Myocardial Infarction, Treatment of, Adrenocortical Dysfunction Therapy, CARDIOVASCULAR DRUGS, Cerebrovascular Diseases, Treatment of, ENDOCRINE DRUGS, IMMUNOMODULATING AGENTS, Immunosuppressants, NEUROLOGIC DRUGS, Stroke, Treatment of, Systemic Lupus Erythematosus, Agents for, Treatment of Disorders of the Coronary Arteries and Atherosclerosis, TREATMENT OF MUSCULOSKELETAL & CONNECTIVE TISSUE DISEASES, Treatment of Other Autoimmune Disorders
Syn. Route 1
Route 1
prasterone can be obtained by two related ways:1) the acetylation of cholesterol (i) with refluxing acetic anhydride gives the corresponding acetate (ii), which is brominated with br2 in acetic acid to the dibromide (iii). the oxidation of (iii) with cro3 in acetic acid followed by debromination with zn in the same solvent and treatment with semicarbazide and sodium acetate in ethanol/water affords 3beta-acetoxyandrost-5-en-17-one semicarbazone (iv), which is finally hydrolyzed with 5n h2so4 in refluxing ethanol.2) the partial silylation of androst-5-ene-3beta,17beta-diol (v) with tert-butyldimethylsilyl chloride and imidazole in dmf yields the 3beta-silyloxy derivative (vi), which is oxidized with cro3-pyridine complex in pyridine affording 3-(tert-butyldimethylsilyloxy)androst-5-en-17-one (vii). finally, this compound is deprotected with hot acetic acid/water/thf or with tetrabutylammonium fluoride in thf.
List of intermediates No.
n-[4-(3-cyano-2-methylpropanoyl)phenyl]acetamide (i)
n-[4-(3-chloro-2-methylpropanoyl)phenyl]acetamide (ii)
4-(4-aminophenyl)-3-methyl-4-oxobutyric acid (iii)
6-(4-aminophenyl)-5-methyl-4,5-dihydro-3(2h)-pyridazinone (iv)
2-pyridinecarbonyl chloride (v)
6-chloro-3-nitro-2-pyridinecarbonitrile (vi)
3,4-dimethoxy-n-methylaniline (vii)
(z)-1-[(e)-2-methoxy-1-methylethenyl]-1-propenyl trimethylsilyl ether; ([(z)-1-[(e)-2-methoxy-1-methylethenyl]-1-propenyl]oxy)(trimethyl)silane
Reference 1:
    fernholz, e.; wallis, e.s.; the preparation of dehydroandrosterone from cholesterol. j am chem soc 1935, 57, 1504-6.
Reference 2:
    casta?er, j.; mealy, n.; rabasseda, x.; prasterone. drugs fut 1995, 20, 6, 575.
Reference 3:
    ruzicka, l.; wettstein, a.; sexual hormones: synthetic preparation of the male sexual hormones trans-dehydroandrosterone and androstene-3,17-dione. helv chim acta 1935, 18, 986-95.
Reference 4:
    fernholz, e.; wallis, e.s.; the constitution of dehydro-androsterone and its preparation from cholesterol. j am chem soc 1935, 57, 1379-80.
Reference 5:
    hosoda, h.; fishman, j.; fukushima, d.k.; convenient, high yield conversion of androst-5-ene-3beta,17beta-diol to dehydroisoandrosterone. j org chem 1973, 38, 24, 4209-11.

来源:药化网

作者:药化小编

摘要:本文合成路线介绍的是药物中文名去氢表雄酮;英文名Dehydroepiandrosterone;Prasterone;PB-007;EL-10;DHEA;GL-701;Fidelin;Anastar;Prestara;Inflabloc;Aslera;CAS[53-43-0]

 
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