C₂₉H₃₅F₂N₅O₆S₂

Base Information

Chemical Name:C₂₉H₃₅F₂N₅O₆S₂
CAS No.:1548337-21-8
Molecular Formula:C₂₉H₃₅F₂N₅O₆S₂
Molecular Weight:651.756
Hs Code.:

C<sub>29</sub>H<sub>35</sub>F<sub>2</sub>N<sub>5</sub>O<sub>6</sub>S<sub>2</sub>

Synonyms:C₂₉H₃₅F₂N₅O₆S₂

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Chemical Property of C₂₉H₃₅F₂N₅O₆S₂

Chemical Property:

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Technology Process of C₂₉H₃₅F₂N₅O₆S₂

There total 6 articles about C₂₉H₃₅F₂N₅O₆S₂ 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:

: 951127-25-6
N-[(2R,3S)-2-(2,5-difluorophenyl)tetrahydro-5-oxo-2H-pyran-3-yl]carbamic acid 1,1-dimethylethyl ester

: 1548337-02-5
C₁₃H₁₆N₄O₃S₂

: 1548337-21-8
C₂₉H₃₅F₂N₅O₆S₂

Guidance literature:: N-[(2R,3S)-2-(2,5-difluorophenyl)tetrahydro-5-oxo-2H-pyran-3-yl]carbamic acid 1,1-dimethylethyl ester; C₁₃H₁₆N₄O₃S₂; With acetic acid; In N,N-dimethyl acetamide; for 0.25h; Inert atmosphere;

With sodium tris(acetoxy)borohydride; In N,N-dimethyl acetamide; at 0 - 20 ℃;

Reference yield:

: 28614-56-4
N-<(4-methylphenyl)sulfonyl>methanesulfonimidoyl chloride

: 1548337-21-8
C₂₉H₃₅F₂N₅O₆S₂

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 2 h / 0 - 20 °C / Inert atmosphere

1.2: 1 h / 0 °C

2.1: dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere

3.1: methanol / chloroform

4.1: acetic acid / N,N-dimethyl acetamide / 0.25 h / Inert atmosphere

4.2: 0 - 20 °C

With methanol; sodium hydride; acetic acid; In tetrahydrofuran; dichloromethane; chloroform; N,N-dimethyl acetamide; mineral oil;

Reference yield:

: 2,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole

: 1548337-21-8
C₂₉H₃₅F₂N₅O₆S₂

Guidance literature:: Multi-step reaction with 5 steps

1.1: triethylamine / tetrahydrofuran; N,N-dimethyl-formamide / 0 - 20 °C / Inert atmosphere

2.1: sodium hydride / tetrahydrofuran; mineral oil / 2 h / 0 - 20 °C / Inert atmosphere

2.2: 1 h / 0 °C

3.1: dichloromethane / 2 h / 0 - 20 °C / Inert atmosphere

4.1: methanol / chloroform

5.1: acetic acid / N,N-dimethyl acetamide / 0.25 h / Inert atmosphere

5.2: 0 - 20 °C

With methanol; sodium hydride; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane; chloroform; N,N-dimethyl acetamide; N,N-dimethyl-formamide; mineral oil;