8-Azabicyclo(3,2,1)oct-2 ene and octane derivatives as cholinergic ligands at nicotinic ACh receptors
The invention disclosed herein relates to novel a 8-azabicyclo[3.2.1]oct-2-ene compound of Formula II, wherein R is hydrogen, methyl, ethyl or benzyl; and R 1 is 3-thienyl, 2-thienyl, 2-(3-methoxymethyl), 3-quinolinyl, 3-benzofuryl, 2-benzofuryl, 3-benzothienyl, 2-benzothienyl, 2-benzothiazolyl, 2-thieno[3.2-b]thienyl, thieno[2.3-b]thienyl, 2-(3-bromo)benzofuryl or 2-(3-bromo)benzothienyl. These compounds are useful for the treatment of conditions or disorders involving the cholinergic system of the central nervous system, pain, inflammatory diseases, diseases caused by smooth muscle contractions and in the cessation of chemical substance abuse.
1. A 8-azabicyclo[3.2.1]oct-2-ene compound of Formula II,
wherein
R is hydrogen, methyl, ethyl or benzyl; and
R 1 is 3-thienyl, 2-thienyl, 2-(3-methoxymethyl)thienyl, 3-quinolinyl, 3-benzofuryl, 2-benzofuryl, 3-benzothienyl, 2-benzothienyl, 2-benzothiazolyl, 2-thieno[3.2-b]thienyl, thieno[2.3-b]thienyl, 2-(3-bromo)benzofuryl or 2-(3-bromo)benzothienyl or a pharmaceutically acceptable addition salt thereof.
2. The 8-azabicyclo[3.2.1]oct-2-ene compound of claim 1 which is
(±)-8-Methyl-3-(3-quinolinyl)-8-azabicyclo[3.2.1]oct-2-ene;
(±)-3-(3-Benzofuryl)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene;
(±)-3-(3-Benzothienyl)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene;
(±)-3-(2-Benzofuryl)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene;
(±)-3-(2-Benzothienyl)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene;
(±)-3-(2-Benzothiazolyl)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene;
(±)-3-(2-Thieno[3.2-b]thienyl)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene;
(±)-3-(2-Thieno[2.3-b]thienyl)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene;
(±)-3-(2-Benzofuryl)-8-H-8-azabicyclo[3.2.1]oct-2-ene;
(±)-3-(2-Benzofuryl)-8-ethyl-8-azabicyclo[3.2.1]oct-2-ene;
(±)-3-[2-(3-Bromobenzofuryl)]-8-methyl-8-azabicyclo[3.2.1]oct-2-ene; or
(±)-3-[2-(3-Bromobenzothienyl)]-8-methyl-8-azabicyclo[3.2.1]oct-2-ene; or a pharmaceutically acceptable addition salt thereof.
3. A pharmaceutical composition, comprising a therapeutically effective amount of a 8-azabicyclo[3.2.1]oct-2-ene compound of claim 1 , or a pharmaceutically acceptable addition salt thereof, together with at least one pharmaceutically acceptable carrier or diluent.
4. A method for the preparation of the 8-azabicyclo[3.2.1]oct-2-ene compound of claim 1 , comprising
a) the step of reacting a compound having the formula
wherein R is as defined in claim 1 ,
with a compound of formula R 1 -X,
wherein R 1 is as defined in claim 1 ,
and X is halogen, boronic acid, or trialkylstannyl; or
b) the step of reducing a compound having the formula
wherein R 1 is as defined in claim 1 .