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11. |
Convenient synthesis of [2‐14C]‐methylglyoxal bis(guanylhydrazone), [14C]‐mitoguazone |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 36,
Issue 1,
1995,
Page 93-96
Alain Burgos,
George J. Ellames,
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摘要:
Abstract[2‐14C]‐Methylglyoxal bis(guanylhydrazone) dihydrochloride, [14C]‐mitoguazone, 3, has been prepared in three steps from potassium [1‐14C]‐acetate in an overall radiochemical yield of 16%. The key steps in this procedure are the formation of the sodium salt of [acetone‐2‐14C]‐methylsulfinylacetone,5, and Pummerer rearrangement to the [14C] labelled hemithioacetal,6, which is trapped with two equivalents of aminoguanidine to afford the desired [14C
ISSN:0362-4803
DOI:10.1002/jlcr.2580360112
出版商:John Wiley&Sons, Ltd.
年代:1995
数据来源: WILEY
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12. |
Synthesis of the enantiomers of [3‐3H]‐2‐[[4‐[(7‐chloro‐4‐quinolinyl)‐amino]pentyl]ethylamino]ethanol, [3‐3H]‐hydroxychloroquine |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 36,
Issue 1,
1995,
Page 97-102
George J. Ellames,
John M. Herbert,
James E. Peace,
David I. Smith,
Karen J. Wedge,
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PDF (240KB)
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摘要:
AbstractThe enantiomers of [3‐3H]‐2‐[[4‐[(7‐chloro‐4‐quinolinyl)amino]pentyl]ethylamino]ethanol,[3‐3H]‐hydroxychloroquine, (R)‐8 and (S)‐8, have been prepared in two steps from the known precursors 4,7‐dichloro‐3‐iodoquinoline,4, and the enantiomers of 2‐[(4‐aminopentyl)ethylamino]ethanol, (R)‐2 and (S)‐2, by formation of the enantiomers of 2‐[[4‐[(7‐chloro‐3‐iodo‐4‐quinolinyl)amino]pentyl]ethylamino]ethanol, (R)‐3 and (S)‐3, and subsequent reductive deiodin
ISSN:0362-4803
DOI:10.1002/jlcr.2580360113
出版商:John Wiley&Sons, Ltd.
年代:1995
数据来源: WILEY
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13. |
Masthead |
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Journal of Labelled Compounds and Radiopharmaceuticals,
Volume 36,
Issue 1,
1995,
Page -
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PDF (92KB)
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ISSN:0362-4803
DOI:10.1002/jlcr.2580360101
出版商:John Wiley&Sons, Ltd.
年代:1995
数据来源: WILEY
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