Preparation of the Phencyclidine Analogues (Part II)
Using a-tetralone, as starting material, a series of phencyclidine analogues were synthesized. This ketone was reacted separately with ethylmagnesium bromide, P-methoxyphenylmagnesium bromide and P-methylphenylmagnesium bromide. The resultant alcohols were treated with a suspension of NaN3 and CCl3C...
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Iranian Institute of Research and Development in Chemical Industries (IRDCI)-ACECR
1993-06-01
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doaj-54c9f01b4b734dc98676794cd1357b5b2020-11-25T03:26:02ZengIranian Institute of Research and Development in Chemical Industries (IRDCI)-ACECRIranian Journal of Chemistry & Chemical Engineering 1021-99861021-99861993-06-01121172110929Preparation of the Phencyclidine Analogues (Part II)Mohammad Raouf Darvich0Afsaneh Zonoozi1Department of Chemistry, Faculty of Science, Tehran University, Tehran, I.R. IRANDepartment of Chemistry, Faculty of Science, Tehran University, Tehran, I.R. IRANUsing a-tetralone, as starting material, a series of phencyclidine analogues were synthesized. This ketone was reacted separately with ethylmagnesium bromide, P-methoxyphenylmagnesium bromide and P-methylphenylmagnesium bromide. The resultant alcohols were treated with a suspension of NaN3 and CCl3COOH in CHCl3. The azides were subsequently reduced with LiAlH4 in dry ether to their primary amines. Cyclization of these amines with 1,5-dibromopentane and 1,4- dibromobutane gave tertiary amines.http://www.ijcce.ac.ir/article_10929_d41d8cd98f00b204e9800998ecf8427e.pdf |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mohammad Raouf Darvich Afsaneh Zonoozi |
spellingShingle |
Mohammad Raouf Darvich Afsaneh Zonoozi Preparation of the Phencyclidine Analogues (Part II) Iranian Journal of Chemistry & Chemical Engineering |
author_facet |
Mohammad Raouf Darvich Afsaneh Zonoozi |
author_sort |
Mohammad Raouf Darvich |
title |
Preparation of the Phencyclidine Analogues (Part II) |
title_short |
Preparation of the Phencyclidine Analogues (Part II) |
title_full |
Preparation of the Phencyclidine Analogues (Part II) |
title_fullStr |
Preparation of the Phencyclidine Analogues (Part II) |
title_full_unstemmed |
Preparation of the Phencyclidine Analogues (Part II) |
title_sort |
preparation of the phencyclidine analogues (part ii) |
publisher |
Iranian Institute of Research and Development in Chemical Industries (IRDCI)-ACECR |
series |
Iranian Journal of Chemistry & Chemical Engineering |
issn |
1021-9986 1021-9986 |
publishDate |
1993-06-01 |
description |
Using a-tetralone, as starting material, a series of phencyclidine analogues were synthesized. This ketone was reacted separately with ethylmagnesium bromide, P-methoxyphenylmagnesium bromide and P-methylphenylmagnesium bromide. The resultant alcohols were treated with a suspension of NaN3 and CCl3COOH in CHCl3. The azides were subsequently reduced with LiAlH4 in dry ether to their primary amines. Cyclization of these amines with 1,5-dibromopentane and 1,4- dibromobutane gave tertiary amines. |
url |
http://www.ijcce.ac.ir/article_10929_d41d8cd98f00b204e9800998ecf8427e.pdf |
work_keys_str_mv |
AT mohammadraoufdarvich preparationofthephencyclidineanaloguespartii AT afsanehzonoozi preparationofthephencyclidineanaloguespartii |
_version_ |
1724594196559429632 |