7149-91-9

Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 29, p. 61, 1986 DOI: 10.1021/jm00151a010

InChI:InChI=1/C10H12O3/c1-7-4-8(6-11)10(13-3)5-9(7)12-2/h4-6H,1-3H3

Upstream product

• 74-90-8 hydrogen cyanide 
• 38064-90-3 2,4-dimethoxytoluene 
• 68-12-2 N,N-dimethyl-formamide 
• 93-61-8 N-methyl-N-phenylformamide 
• 613-45-6 2,4-Dimethoxybenzaldehyde 
• 17715-69-4 1-Bromo-2,4-dimethoxybenzene 

Downstream Products

• 24953-82-0 1,3-dimethoxy-4,6-dimethylbenzene 
• 171670-26-1 2,4-dimethoxy-5-methylphenylmethanol 
• 50625-55-3 5-methyl-2,4-dimethoxy-benzoic acid 
• 615-89-4 2,4-dimethyl-5-hydroxyphenol 
• 37467-68-8 1-(2,6-dihydroxy-3,5-dimethyl-phenyl)-ethanone 
• 864514-27-2 2-{(2R,3S)-5-[(2R,4R,6S)-4-(tert-Butyl-dimethyl-silanyloxy)-6-cyano-3,3-dimethyl-tetrahydro-pyran-2-yl]-2-hydroxy-3-methyl-4-oxo-pentyl}-4,6-bis-(4-methoxy-benzyloxy)-3-methyl-benzoic acid methyl ester 
• 1402588-78-6 C₄₆H₅₃NO₁₀ 
• 1402588-79-7 C₅₀H₇₃NO₉Si₂ 
• 1402588-84-4 C₅₁H₈₃NO₁₂Si₂ 
• 1402589-26-7 C₅₁H₈₃NO₁₂Si₂ 
• 19672-08-3 3-(4,6-Dimethoxy-3-methyl-phenoxy)-butanon-⁽²⁾ 
• 91971-25-4 2,6-dimethoxy-3,5-dimethylbenzoic acid 

Relevant academic research and scientific papers

Studies toward the unique pederin family member psymberin: Full structure elucidation, two alternative total syntheses, and analogs

Two synthetic approaches to psymberin have been accomplished. A highly convergent first generation synthesis led to the complete stereochemical assignment and demonstrated that psymberin and irciniastatin A are identical compounds. This synthesis featured

BENZOFURAN AND BENZOTHIOPHENE-2-CARBOXYLIC ACID AMIDE DERIVATIVES

The present invention relates to compounds of formula I wherein X, A and R1 to R4 are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prevention of diseases which are associated with the modulation of H3 receptors.

Potential neuroleptic agents. 4. Chemistry, behavioral pharmacology, and inhibition of [3H]spiperone binding of 3,5-disubstituted N-[(1-ethyl-2-pyrrolidinyl)methyl]-6-methoxysalicylamides

A series of 3,5-disubstituted N-[(1-ethyl-2-pyrrolidinyl)methyl]-6-methoxysalicylamides was synthesized, starting from the 2,6-dimethoxybenzoic acids, by boron tribromide demethylation of the corresponding 3,5-disubstituted 2,6-dimethoxybenzamides and sep