123486-12-4

Upstream product

• 118431-79-1 2-[(3-nitrophenyl)methylene]-3-oxobutanoic acid,1-methylethyl ester 
• 108931-52-8 1,4-Dihydro-2-methoxy-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid,1-methylethyl ester 
• 7693-46-1 4-Nitrophenyl chloroformate 

Downstream Products

• 112770-77-1 (4R)-1,4-dihydro-2-<<(4-methoxyphenyl)methyl>thio>-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid 1-methylethyl ester 
• 128162-87-8 (4S)-1,4-dihydro-2-methoxy-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid 1-methylethyl ester 
• 128162-86-7 (4R)-1,4-dihydro-2-methoxy-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid 1-methylethyl ester 
• 832075-56-6 3,6-dihydro-4-methyl-6-(3-nitrophenyl)-2-oxo-1,5(2H)-pyrimidinedicarboxylic acid 5-(1-methylethyl) 1-<(S)-1-methyl-2-ethyl> diester 
• 112795-83-2 1-(aminocarbonyl)-1,2,3,6-tetrahydro-4-methyl-6-(3-nitrophenyl)-2-oxo-5-pyrimidinecarboxylic acid 1-methylethyl ester 
• 123485-96-1 3,6-dihydro-4-methyl-6-(3-nitrophenyl)-2-0x0-1,5(2H)-pyrimidinedicarboxylic acid 5-(1-methylethyl) 1-(4-nitrophenyl) diester 
• 113094-77-2 <1(R)>-1,6-dihydro-2-methoxy-4-methyl-6(R)-(4-nitrophenyl)-1-<<(1-phenylethyl)amino>carbonyl>-5-pyrimidine carboxylic acid 1-methylethyl ester 
• 113116-81-7 <1(R)>-1,6-dihydro-2-methoxy-4-methyl-6(S)-(4-nitrophenyl)-1-<<(1-phenylethyl)amino>carbonyl>-5-pyrimidine carboxylic acid 1-methylethyl ester 

Relevant academic research and scientific papers

Dihydropyrimidine Calcium Channel Blockers. 2. 3-Substituted-4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic Acid Esters as Potent Mimics of Dihydropyridines

To enhance the intrinsic potency of dihydropyrimidine calcium channel blockers, we have modified the structure of previously described 2-heteroalkyl-1,4-dihydropyrimidines 2 to 3-substituted 1,4-dihydropyrimidines 3.Structure-activity studies using potass

3-oxo-1,2,4-triazolo(4,3-A) pyrimidine-6-carboxylic acid esters

Compounds having the formula STR1 and pharmaceutically acceptable salts thereof, wherein R4 is aryl are disclosed. These novel compounds are useful, for example, as cardiovascular agents.