Farnesyl transferase inhibiting 1,2-annelated quinoline enantiomer
View Patent ↗(−)-5-(3-Chlorophenyl)-α-(4-chlorophenyl)-α-(1-methyl-1H-imidazol-5-yl)tetrazolo-[1,5-a]quinazoline-7-methanamine and its pharmaceutically acceptable acid addition salts, and the use of such compounds in medicine especially for the treatment of cancer.
1. A compound comprising: (−)-5-(3-Chlorophenyl)-α-(4-chlorophenyl)-α-(1-methyl-1H-imidazol-5-yl)tetrazolo[1,5-a]quinazoline-7-methanamine or a pharmaceutically acceptable acid addition salt thereof.
2. A compound comprising: (−)-5-(3-Chlorophenyl)-α-(4-chlorophenyl)-α-(1-methyl-1H-imidazol-5-yl)-tetrazolo[1,5-a]quinazoline-7-methanamine.
3. A pharmaceutical composition comprising the compound of claim 1 in a pharmaceutically acceptable carrier.
4. A pharmaceutical composition comprising the compound of claim 2 in a pharmaceutically acceptable carrier.
5. A pharmaceutical composition of claim 3 in a dosage unit form.
6. The pharmaceutical composition of claim 5 comprising 50 to 300 mg of active ingredient in each unit dosage form.
7. The pharmaceutical composition of claim 6 in the form of a tablet.
8. A process for preparing a pharmaceutical composition as claimed in claim 3 wherein a therapeutically effective amount of the active ingredient is intimately mixed with a pharmaceutically acceptable carrier.
9. A process for the preparation of the compound of claim 1 which comprises treating (±)-5-(3-chlorophenyl)-α-(4-chlorophenyl)-α-(1-methyl-1H-imidazol-5-yl)tetrazolo[1,5-a]quinazoline-7-methanamine or a pharmaceutically acceptable acid addition salt thereof to separate the constituent (+) and (−) enantiomers and isolating the (−) enantiomer or a pharmaceutically acceptable acid addition salt thereof.