405239-75-0

Usage

InChI:InChI=1/C38H49N3O7/c1-37(2,3)47-35(42)32-28(26-10-9-19-41(21-26)36(43)48-38(4,5)6)20-29(40-34(32)39)33-30(45-22-24-13-14-24)11-8-12-31(33)46-23-25-15-17-27(44-7)18-16-25/h8,11-12,15-18,20,24,26H,9-10,13-14,19,21-23H2,1-7H3,(H2,39,40)

Upstream product

• 1116-98-9 cyanoacetic acid tert-butyl ester 
• 118156-93-7 3-formylpiperidine-1-carboxylic acid tert-butyl ester 
• 405239-71-6 1-{2-(cyclopropylmethoxy)-6-[(4-methoxybenzyl)oxy]phenyl}ethanone 

Downstream Products

• 406212-99-5 tert-butyl 3-[2-amino-6-{2-(cyclopropylmethoxy)-6-[(4-methoxybenzyl)oxy]-phenyl}-3-(hydroxymethyl)-4-pyridinyl]-1-piperidinecarboxylate 

Relevant academic research and scientific papers

AN OPTICALLY ACITVE PYRIDINE DERIVATIVE AND A MEDICAMENT CONTAINING THE SAME

An optically active (-)-7-[2-(cyclopropylmethoxy)-6-hydroxyphenyl]-5-[(3S)-3-piperidinyl]-1,4-dihydro-2H-pyrido [2,3-d][1,3]oxazin-2-one of the formula (I) or salt thereof. The compound has an excellent anti-inflammatory activity, and other biological act

Pyridine derivatives

Pyridine compounds of general formula: wherein —R1represents in which R11is hydrogen, C1-6alkyl, halogen, hydroxy, C1-12alkoxy, nitro, amino, C1-6alkylsulfonylamino, C1-6alkoxycarbonyl, C1-6alkylamino, di(C1-6alkyl)amino, C1-6alkanoylamino, phenyl C1-6alkylamino, phenylsulfonylamino, or —O—(CH2)n—R111; R2represents hydrogen or halogen; R3represents hydrogen, —CR31R32R33, or —NR34R35; R4is hydrogen, carbamoyl, CN, carboxyl, etc.; R5is amino, C1-6alkylamino, di C1-6alkylamino, etc. or salt thereof. The compound has an excellent anti-inflammatory activity, and other biological activity.