Studies on the Synthesis of Antipyretic Analgesics. V
Torizo Takahashi, Yoshiharu Matsuo, Ken Kanematsu
Abstract
Open-access reader
Torizo Takahashi, Yoshiharu Matsuo, Ken Kanematsu
Abstract
Open-access reader
Having some doubts about the position (N or N′) at which the acyl group is introduced in acylation of N-antipyrinyl-2-methylalanine amide (VIII), reported in the preceding paper, introduction of acyl group was examined in the most simple of the compounds with similar structure N-antipyrinylglycine amide (I). Comparison of infrared spectra of N-acetyl-N-antipyrinylglycine amide (II) and (VIII) proved that acylation of these compounds resulted in introduction of acyl group into N. Haloacylation of (I) Was also proved to give N-substituted compound.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Having some doubts about the position (N or N′) at which the acyl group is introduced in acylation of N-antipyrinyl-2-methylalanine amide (VIII), reported in the preceding paper, introduction of acyl group was examined in the most simple of the compounds with similar structure N-antipyrinylglycine amide (I). Comparison of infrared spectra of N-acetyl-N-antipyrinylglycine amide (II) and (VIII) proved that acylation of these compounds resulted in introduction of acyl group into N. Haloacylation of (I) Was also proved to give N-substituted compound.
Key concepts: Acylation, Amide, Chemistry, Antipyretic, Stereochemistry, Medicinal chemistry, Organic chemistry, Pharmacology