Sodium Hydroxide → HCID 13218156, compound
Reaction equation
[C:1]([C@@H:5]1[CH2:9][C:8](=[CH2:10])[CH2:7][C@H:6]1[C:11]([O:13]C)=[O:12])([O:3]C)=[O:2].[OH-].[Na+]>>[CH2:10]=[C:8]1[CH2:7][C@@H:6]([C:11]([OH:13])=[O:12])[C@H:5]([C:1]([OH:3])=[O:2])[CH2:9]1Participants
Procedure
It is disclosed in U.S. Pat. No. 5,140,023 and U.S. Pat. No. 5,223,613 that such azanoradamantane compounds can be prepared by reacting a trans-1,2-dicarbomethoxy-4-methylenecyclopentane with sodium hydroxide, followed by reaction with an acid to produce trans-4-methylene-1,2-cyclopentane-dicarboxylic acid. The dicarboxylic acid is reacted with acetic anhydride to produce cis-tetrahydro-5-methylene-1H-cyclopenta[c]furan-1,3(3aH)-dione which is reacted with ammonia gas and methylene chloride to produce the ammonium salt. Reaction of the ammonium salt with acetyl chloride produces the amide which is reacted with lithium aluminum hydride and di-t-butyl dicarbonate to produce cis-1,1-dimethylethylhexahydro-5-methylene-cyclopenta[c]pyrrole-2(1H)-carboxylate. The product is reacted with bis(p-toluenesulfonyl)-sulfodiimide to produce the p-toluenesulfonamide which is reacted with thexyl borane to produce an endo-alcohol. The endo-alcohol is reacted with p-toluenesulfonyl chloride to produce a tosylate which is reacted with trifluoroacetic acid and treated with Hunig's base to provide the p-toluenesulfonamide azacycle. The azacycle is reductively cleaved to produce the aminoazacycle which is coupled with a benzoic acid derivative under mixed anhydride conditions to give the protected benzamide azacycle. Deprotection by hydrolysis and treatment with hydrochloric acid produces the desired benzamide azacycles.
Workup
- custom5,223,613 that such azanoradamantane compounds can be prepared
- customfollowed by reaction with an acid
Sources & evidence
- ORD record
- ord-048a7285f9cb4301b404a1c16b6a58ce
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05650535
Reaction notes
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