Category: 38309-60-3

Awesome and Easy Science Experiments about 3H-Spiro[2-benzofuran-1,4′-piperidine]

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Product Details of 38309-60-3, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 38309-60-3

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent£¬ Product Details of 38309-60-3, Which mentioned a new discovery about 38309-60-3

SPIROPIPERIDINE GLYCINAMIDE DERIVATIVES

In particular, the present invention is concerned with compounds of the general formula (I)wherein X, Y and R1 to R10 are as described herein. The compounds are V1a receptor antagonists. The invention also relates to the manufacture of compounds of formula I, pharmaceutical compositions containing them and their use for the treatment of anxiety and depressive disorders and other diseases.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Product Details of 38309-60-3, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 38309-60-3

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H11640N – PubChem

 

Analyzing the synthesis route of 38309-60-3

The synthetic route of 38309-60-3 has been constantly updated, and we look forward to future research findings.

38309-60-3, 3H-Spiro[2-benzofuran-1,4′-piperidine] is a piperidines compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

Example 205 (S)-1-(2-(5-methyl-1,3,4-oxadiazol-2-yl)benzo(b)furan-4-yloxy)-3-(1,3-dihydrobenzo(c)furan-1-spiro-4′-piperidin-1′-yl)-2-propanol 1/4 hydrate By the reactions in the same manner as in Example 1 using (S)-5-(4-glycidyloxybenzo(b)furan-2-yl)-2-methyl-1,3,4-oxadiazole and 1,3-dihydrobenzo(c)furan-1-spiro-4′-piperidine, the title compound was obtained as white crystals, melting point 198-199 C.

The synthetic route of 38309-60-3 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; Nishiyama, Akira; Bougauchi, Masahiro; Kuroita, Takanobu; Minoguchi, Masanori; Morio, Yasunori; Kanzaki, Kouji; US2002/111358; (2002); A1;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem