1255707-32-4Relevant articles and documents
Intermediates for preparing roflumilast 3-cyclopropyl-methoxy-4-difluoro methoxybenzoic acid
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Paragraph 0040; 0041, (2017/03/08)
The invention discloses a preparation method of roflumilast intermediate 3-cyclopropyl methoxyl-4-(difluoromethoxy)benzoic acid. A raw material of 3-hydroxy-4-benzyloxy benzaldehyde is subjected to 3-hydroxy cyclopropane methylation to convert aldehyde group to methyl carboxylate; then the material is subjected to catalytic hydrogenation to remove 4-benzyl group and subjected to difluoro methoxylation; and then the reaction product is hydrolyzed to obtain the 3-cyclopropyl methoxyl-4-(difluoromethoxy)benzoic acid. The method has the advantages of simple operation, mild reaction conditions and high regioselectivity, and is suitable for industrialized production.
1-PHENYL-2-PYRIDINYL ALKYL ALCOHOL DERIVATIVES AS PHOSPHODIESTERASE INHIBITORS
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Paragraph 0464; 0467, (2014/06/23)
Compounds of formula (I) described herein are inhibitors of the phosphodiesterase 4 (PDE4) enzyme and are useful for the prevention and/or treatment of an allergic disease state or a disease of the respiratory tract characterized by airway obstruction.
BIS-(SULFONYLAMINO) DERIVATIVES FOR TREATMENT OF PAIN AND INFLAMMATION
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Page/Page column 46, (2010/12/17)
The invention provides compounds of formula (I) wherein R1, R2, R3, A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together