C₂₄H₃₂N₈O₇S₃

Base Information

Chemical Name:C₂₄H₃₂N₈O₇S₃
CAS No.:884335-07-3
Molecular Formula:C₂₄H₃₂N₈O₇S₃
Molecular Weight:640.765
Hs Code.:

C<sub>24</sub>H<sub>32</sub>N<sub>8</sub>O<sub>7</sub>S<sub>3</sub>

Synonyms:C₂₄H₃₂N₈O₇S₃

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₄H₃₂N₈O₇S₃

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Technology Process of C₂₄H₃₂N₈O₇S₃

There total 10 articles about C₂₄H₃₂N₈O₇S₃ 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: 95.0%

: 884335-06-2
C₂₄H₃₀N₈O₉S₄

: 884335-07-3
C₂₄H₃₂N₈O₇S₃

Guidance literature:: With water; In acetonitrile; at 70 ℃;
DOI:10.1021/ja0608545

Reference yield:

: 884335-03-9
Toluene-4-sulfonic acid 4-((4R,5S)-5-hydroxy-2,2-dioxo-2λ⁶-[1,2,3]oxathiazinan-4-yl)-but-3-ynyl ester

: 884335-07-3
C₂₄H₃₂N₈O₇S₃

Guidance literature:: Multi-step reaction with 10 steps

1.1: H₂ / Pd/CaCO₃/Pb / tetrahydrofuran

2.1: NaN₃; nBu₄NI / dimethylformamide

3.1: 85 percent / nBu₄NI; K₂CO₃ / acetonitrile

4.1: Me₃P; H₂O / tetrahydrofuran

5.1: iPr₂NEt / acetonitrile

6.1: pyridine; DMAP / CH₂Cl₂

7.1: NaN₃ / dimethylformamide / -15 °C

8.1: 74 percent / (NH₄)2Ce(NO₃)6 / CH₂Cl₂; 2-methyl-propan-2-ol

9.1: tBuOK

9.2: 70 percent / (Me₃Si)2NH

10.1: 95 percent / H₂O / acetonitrile / 70 °C

With pyridine; dmap; sodium azide; ammonium cerium(IV) nitrate; potassium tert-butylate; water; hydrogen; tetra-(n-butyl)ammonium iodide; potassium carbonate; N-ethyl-N,N-diisopropylamine; trimethylphosphane; Lindlar's catalyst; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;
DOI:10.1021/ja0608545

Reference yield:

: 884335-17-5
(4R,5S)-4-((Z)-4-Azido-but-1-enyl)-2,2-dioxo-2λ⁶-[1,2,3]oxathiazinan-5-ol

: 884335-07-3
C₂₄H₃₂N₈O₇S₃

Guidance literature:: Multi-step reaction with 8 steps

1.1: 85 percent / nBu₄NI; K₂CO₃ / acetonitrile

2.1: Me₃P; H₂O / tetrahydrofuran

3.1: iPr₂NEt / acetonitrile

4.1: pyridine; DMAP / CH₂Cl₂

5.1: NaN₃ / dimethylformamide / -15 °C

6.1: 74 percent / (NH₄)2Ce(NO₃)6 / CH₂Cl₂; 2-methyl-propan-2-ol

7.1: tBuOK

7.2: 70 percent / (Me₃Si)2NH

8.1: 95 percent / H₂O / acetonitrile / 70 °C

With pyridine; dmap; sodium azide; ammonium cerium(IV) nitrate; potassium tert-butylate; water; tetra-(n-butyl)ammonium iodide; potassium carbonate; N-ethyl-N,N-diisopropylamine; trimethylphosphane; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;
DOI:10.1021/ja0608545