147698-99-5

Upstream product

• 107813-00-3 4-Chloro-2-[1-(3-nitro-phenyl)-meth-(Z)-ylidene]-3-oxo-butyric acid methyl ester 
• 920312-63-6 ethyl (Z)-3-(4-ethoxyphenylamino)but-2-enoate 

Downstream Products

• 147699-02-3 2-[1-Chloro-meth-(Z)-ylidene]-1-(4-ethoxy-phenyl)-6-methyl-4-(3-nitro-phenyl)-1,2,3,4-tetrahydro-pyridine-3,5-dicarboxylic acid 5-ethyl ester 3-methyl ester 

Relevant academic research and scientific papers

N-aryl-2-hydroxy-1,2,3,4-tetrahydropyridines and N-aryl-2-chloromethylene-1,2,3,4-tetrahydropyridines - Successive intermediates in the Hantzsch synthesis of 1,4-dihydropyridines

Esters of 4-chloro-2-arylideneacetoacetic acid I and esters of N-arylaminocrotonic acid II form stable N-aryl-3,4-trans-2-hydroxy-1,2,3,4-tetrahydropyridines III. Their regio- and stereoselective dehydration results in N-aryl-2-chloromethylene-1,2,3,4-tetrahydropyridines with an exocyclic bond, IV. Compounds IV isomerize to the corresponding N-aryl-2-chloromethyl-1,4-dihydropyridines V in acid medium. Michael addition of compounds I and II in chloroform or benzene forms carbocyclic derivatives of cyclohexene VI. 1998 Plenum Publishing Corporation.