C₂₆H₃₅N₃O₅S

Base Information

Chemical Name:C₂₆H₃₅N₃O₅S
CAS No.:1380434-65-0
Molecular Formula:C₂₆H₃₅N₃O₅S
Molecular Weight:501.647
Hs Code.:

C<sub>26</sub>H<sub>35</sub>N<sub>3</sub>O<sub>5</sub>S

Synonyms:C₂₆H₃₅N₃O₅S

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Chemical Property of C₂₆H₃₅N₃O₅S

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Technology Process of C₂₆H₃₅N₃O₅S

There total 7 articles about C₂₆H₃₅N₃O₅S which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 78.0%

: 1380434-64-9
C₃₂H₄₉N₃O₅SSi

: 1380434-65-0
C₂₆H₃₅N₃O₅S

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1021/jm300259r

Reference yield:

: [2-methylthiopyrazolo[1,5-a]pyridin-3-yl]amine

: 1380434-65-0
C₂₆H₃₅N₃O₅S

Guidance literature:: Multi-step reaction with 7 steps

1.1: triethylamine / dichloromethane / 16 h / 20 °C / Cooling with ice

2.1: n-butyllithium / tetrahydrofuran; hexane / 1 h / -78 °C / Inert atmosphere

2.2: 0.17 h / -78 °C / Inert atmosphere

3.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; barium hydroxide octahydrate / 1,2-dimethoxyethane; water / 4 h / 90 °C / Inert atmosphere

4.1: sodium hydride / N,N-dimethyl-formamide / 3 h / 20 - 50 °C

5.1: hydrogenchloride / ethyl acetate / 1 h / 20 °C

6.1: sodium tris(acetoxy)borohydride / tetrahydrofuran; acetic acid / 20 °C

7.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With hydrogenchloride; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; barium hydroxide octahydrate; tetrabutyl ammonium fluoride; sodium tris(acetoxy)borohydride; sodium hydride; triethylamine; In tetrahydrofuran; 1,2-dimethoxyethane; hexane; dichloromethane; water; acetic acid; ethyl acetate; N,N-dimethyl-formamide; 3.1: Suzuki coupling;
DOI:10.1021/jm300259r

Reference yield:

: 1380434-70-7
tert-butyl (7-(2,6-dimethoxy-4-(methoxymethyl)phenyl)-2-(methylthio)pyrazolo[1,5-a]pyridin-3-yl)((tetrahydro-2H-pyran-4-yl)methyl)carbamate

: 1380434-65-0
C₂₆H₃₅N₃O₅S

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride / ethyl acetate / 1 h / 20 °C

2: sodium tris(acetoxy)borohydride / tetrahydrofuran; acetic acid / 20 °C

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

With hydrogenchloride; tetrabutyl ammonium fluoride; sodium tris(acetoxy)borohydride; In tetrahydrofuran; acetic acid; ethyl acetate;
DOI:10.1021/jm300259r