Process for preparing 3,6-dihydro-1,3,5-triazine derivatives
A process for the synthesis of 3,6-dihydro-1,3,5-triazine derivatives is claimed wherein a biguanid is reacted with acetaldehyde in the presence of an inorganic and/or organic base. The process can be carried out at mild and therefore economical reaction conditions.
1. A process for preparing a compound of formula I:
in which
R 1 , R 2 , R 3 and R 4 are chosen independently from the following groups:
H;
C 1 -C 20 -alkyl optionally substituted by halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy or C 3 -C 8 -cycloalkyl;
C 2 -C 20 -alkenyl optionally substituted by halogen, C 1 -C 5 -alkyl or C 1 -C 5 -alkoxy; C 2 -C 20 -alkynyl optionally substituted by halogen, C 1 -C 5 -alkyl or C 1 -C 5 -alkoxy; C 3 -C 8 -cycloalkyl optionally substituted by C 1 -C 5 -alkyl or C 1 -C 5 -alkoxy; C 3 -C 8 -heterocycloalkyl having one or more hetero atoms chosen from N, O and S and optionally substituted by C 1 -C 5 -alkyl or C 1 -C 5 -alkoxy; C 6 -C 14 -aryl-(C 1 -C 20 )alkyl optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl, C 1 -C 5 -alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl;
C 6 -C 14 -aryl optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy;
C 1 -C 13 -heteroaryl having one or more hetero atoms chosen from N, O and S and optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl-(C 1 -C 5 )-alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl;
R 1 and R 2 , on the one hand, and R 3 and R 4 , on the other hand, optionally forming with the nitrogen atom an n-membered ring (n between 3 and 8) optionally comprising one or more hetero atoms chosen from N, O and S and optionally being substituted by one of the following groups: amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl-(C 1 -C 5 )-alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl;
R 5 is chosen from the following groups:
C 1 -C 20 -alkyl optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl-(C 1 -C 5 -)-alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl;
C 2 -C 20 -alkenyl optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl-(C 1 -C 5 )-alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl;
C 2 -C 20 -alkynyl optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl-(C 1 -C 5 )-alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl;
C 3 -C 8 -cycloalkyl optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl-(C 1 -C 5 )-alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl;
C 3 -C 8 -heterocycloalkyl having one or more hetero atoms chosen from N, O and S and optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl-(C 1 -C 5 )-alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl;
C 6 -C 14 -aryl optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl-(C 1 -C 5 )-alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl;
C 1 -C 13 -heteroaryl having one or more hetero atoms chosen from N, O and S and optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl-(C 1 -C 5 )-alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl;
C 6 -C 14 -aryl-(C 1 -C 5 )-alkyl optionally substituted by amino, hydroxyl, mercapto, halogen, C 1 -C 5 -alkyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkylthio, C 1 -C 5 -alkylamino, C 6 -C 14 -aryl-oxy, C 6 -C 14 -aryl-(C 1 -C 5 )-alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
or a pharmaceutically usable derivative, solvate, salt or stereoisomer thereof,
said process comprising reacting a compound of the formula II:
in which R 1 , R 2 , R 3 , R 4 are as defined above,
with a compound of the formula III:
R 5 —CHO III
in which R 5 is as defined above,
in a polar solvent or solvant mixture in presence of an inorganic and/or organic base.
2. Process according to claim 1 ,
in which R 1 , R 2 are independently from each other C 1 -C 20 -alkyl; R 3 and R 4 are H; and R 5 is C 1 -C 20 -alkyl (C1-C20).
3. Process according to claim 1 ,
in which R 1 , R 2 are independently C 1 -C 6 -alkyl; R 3 and R 4 are H; and R 5 is C 1 -C 6 -alkyl.
4. Process according to claim 1 ,
in which R 1 and R 2 are methyl; R 3 and R 4 are H and R 5 is methyl.
5. Process according to claim 1 , in which the base is chosen from alkali hydroxides, alkali carbonates and alkali alcoholates or organic bases chosen from triethyl amine, diisopropylethyl amine, pyridine, pyrrol, pyrrolidine, and piperidine, and any mixtures thereof.
6. Process according to claim 1 , in which the solvent is chosen from water, methanol, ethanol, isopropanol, n-butanol, 2-butanol, i-butanol, t-butanol, N,N-dimethyl formamide and any mixtures thereof.
7. Process according to claim 1 , in which the concentration of compound of formula III is from 1 equivalent to 10 equivalents based on the compound of the formula II.
8. Process according to claim 1 , in which the base is present in an amount from 0.5 equivalents to 10 equivalents based on the compound of formula II.
9. Process according to claim 1 , in which the compound of formula III is acetaldehyde.
10. Process according to claim 1 , in which the reaction is performed under ambient pressure.
11. Process according to claim 1 , in which the reaction is performed at room temperature.