C₂₄H₂₀BrN₇O₆S

Base Information

Chemical Name:C₂₄H₂₀BrN₇O₆S
CAS No.:1429313-31-4
Molecular Formula:C₂₄H₂₀BrN₇O₆S
Molecular Weight:614.436
Hs Code.:

C<sub>24</sub>H<sub>20</sub>BrN<sub>7</sub>O<sub>6</sub>S

Synonyms:C₂₄H₂₀BrN₇O₆S

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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 C₂₄H₂₀BrN₇O₆S

Chemical Property:

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Technology Process of C₂₄H₂₀BrN₇O₆S

There total 5 articles about C₂₄H₂₀BrN₇O₆S 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:

: 136918-14-4,85-41-6
phthalimide

: 1429313-30-3
C₁₆H₁₇BrN₆O₅S

: 1429313-31-4
C₂₄H₂₀BrN₇O₆S

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 5 - 20 ℃; for 2h; Inert atmosphere;

Reference yield:

: 214000-16-5
N-(tert-butoxycarbonyl)-N'-(2-nitrobenzenesulfonyl)ethylenediamine

: 1429313-31-4
C₂₄H₂₀BrN₇O₆S

Guidance literature:: Multi-step reaction with 5 steps

1: caesium carbonate / N,N-dimethyl-formamide / 50 °C

2: water; sodium hydroxide / methanol / 1.5 h / 20 °C

3: acetyl chloride / 2 h / 20 °C

4: N-ethyl-N,N-diisopropylamine / acetonitrile / Reflux

5: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h / 5 - 20 °C / Inert atmosphere

With di-isopropyl azodicarboxylate; water; caesium carbonate; N-ethyl-N,N-diisopropylamine; acetyl chloride; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1429313-27-8
C₁₇H₂₅N₃O₈S

: 1429313-31-4
C₂₄H₂₀BrN₇O₆S

Guidance literature:: Multi-step reaction with 4 steps

1: water; sodium hydroxide / methanol / 1.5 h / 20 °C

2: acetyl chloride / 2 h / 20 °C

3: N-ethyl-N,N-diisopropylamine / acetonitrile / Reflux

4: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 2 h / 5 - 20 °C / Inert atmosphere

With di-isopropyl azodicarboxylate; water; N-ethyl-N,N-diisopropylamine; acetyl chloride; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; methanol; acetonitrile;