Benzazepine dicarboxamide compounds
This invention relates to novel benzazepine dicarboxamide compounds of the formula wherein R 1 to R 4 are as defined in the description and in the claims, as well as pharmaceutically acceptable salts thereof. These compounds are TLR agonists and may therefore be useful as medicaments for the treatment of diseases such as cancer, autoimmune diseases, inflammation, sepsis, allergy, asthma, graft rejection, graft-versus-host disease, immunodeficiencies, and infectious diseases.
1. A process for the preparation of 2-amino-8-methoxycarbonyl-3H-1-benzazepine-4-carboxylic acid (I) comprising the step of deprotection of
4-tert-butyl 8-methyl 2-amino-3H-benzo[b]azepine-4,8-dicarboxylate (II) under acidic conditions.
2. The process according to claim 1 said process further comprising the step of
reductive cyclization of compound (III) by treating compound (III) with iron and acetic acid.
3. The process according to claim 2 said process further comprising condensation of tert-butyl 3-cyano-2-(triphenylphosphoranylidene)propanoate with methyl 4-formyl-3-nitrobenzoate under basic conditions to afford methyl 4-(3-(tert-butoxy)-2-(cyanomethyl)-3-oxoprop-1-en-1-yl)-3-nitrobenzoate
4. A process for the preparation compound according to formula (VI) comprising
condensation of VIII with VII basic conditions to afford methyl 4-(3-(tert-butoxy)-2-(cyanomethyl)-3-oxoprop-1-en-1-yl)-3-nitrobenzoate wherein R a and R b are C 1-6 alkyl or benzyl.
5. A compound which compound is 2-amino-8-methoxycarbonyl-3H-1-benzazepine-4-carboxylic acid, 4-tert-butyl 8-methyl 2-amino-3H-benzo[b]azepine-4,8-dicarboxylate or tert-butyl 3-cyano-2-(triphenylphosphoranylidene)propanoate.