CHEMICAL PROCESS
The present invention provides, inter alia, a process for producing a compound of formula (I) wherein the substituents are as defined in claim 1. The present invention further provides intermediate compounds utilised in said process, and methods for producing said intermediate compounds.
1 . A process for the preparation of a compound of formula (I) or a salt thereof:
wherein
R 1 is C 3 -C 7 cycloalkyl;
said process comprising:
reacting a compound of formula (II)
with a compound of formula (III)
wherein R 1 a is C 3 -C 7 cycloalkyl and X is halogen or hydroxy; or
R 1a is C 3 -C 7 cycloalkenyl and X is hydrogen;
in the presence of an acid to give a compound of formula (I).
2 . A process according to claim 1 , wherein R 1 is cyclopentyl or cyclohexyl.
3 . A process according to claim 1 , wherein a compound of formula (III) is selected from the group consisting of chlorocyclopentane, chlorocyclohexane, cyclopentanol, cyclohexanol, cyclopentene and cyclohexene.
4 . A process according to claim 1 , wherein R 1 is cyclohexyl and the compound of formula (III) is chlorocyclohexane or cyclohexanol.
5 . A process according to claim 1 , wherein the acid is a lewis acid.
6 . A process according to claim 5 , wherein the lewis acid is selected from the group consisting of aluminium(III) chloride, iron(III) chloride, titanium(IV) chloride, zirconium(IV) chloride and zirconium(IV) oxide chloride.
7 . A process according to claim 6 , wherein the lewis acid is aluminium(III) chloride.
8 . A process according to claim 1 , wherein the compound of formula (II) is used in an amount of at least 2 molar equivalents per mole of a compound of formula (III).
9 . A process according to claim 1 , wherein the compound of formula (II) is used in an amount of from 3 to 5 molar equivalents per mole of a compound of formula (III).
10 . A process according to claim 1 , wherein the acid is used in an amount of at least 1.1 molar equivalents per mole of a compound of formula (II).
11 . A process according to claim 1 , wherein the compound of formula (I) is further reacted with a compound of formula (IV),
wherein Y is a suitable leaving group and R 2 is hydrogen or C 1 -C 6 alkyl;
to give a compound of formula (V),
wherein R 1 is as defined in claim 1 and R 2 is as defined above.
12 . A process according to claim 11 , wherein Y is chloro.
13 . A process according to claim 1 , wherein the compound of formula (I) is further converted to a compound of formula (VI)
wherein R 1 is as defined in claim 1 .
14 . A process according to claim 11 , wherein the compound of formula (V) is further converted to a compound of formula (VI)
15 . A compound selected from the group consisting of a compound of formula (V-I), (V-II), (V-III) and (V-IV) below,
16 . Use of a compound of formula (I),
wherein R 1 is as defined in claim 1 , for preparing a compound of formula (VI).