C₂₅H₃₁N₇O₅S

Base Information

Chemical Name:C₂₅H₃₁N₇O₅S
CAS No.:1542268-37-0
Molecular Formula:C₂₅H₃₁N₇O₅S
Molecular Weight:541.631
Hs Code.:

C<sub>25</sub>H<sub>31</sub>N<sub>7</sub>O<sub>5</sub>S

Synonyms:C₂₅H₃₁N₇O₅S

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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 C₂₅H₃₁N₇O₅S

Chemical Property:

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Technology Process of C₂₅H₃₁N₇O₅S

There total 9 articles about C₂₅H₃₁N₇O₅S 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:

: 170961-15-6
tert-butyl 1,3-thiazole-2-yl-carbamate

: 1542268-37-0
C₂₅H₃₁N₇O₅S

Guidance literature:: Multi-step reaction with 3 steps

1: lithium diisopropyl amide / tetrahydrofuran / -78 °C

2: bis-triphenylphosphine-palladium(II) chloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 95 °C / Inert atmosphere

3: sodium hydride / acetonitrile / 2 h / 20 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; sodium hydride; N-ethyl-N,N-diisopropylamine; lithium diisopropyl amide; In tetrahydrofuran; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 20877-09-2
4-(dimethylcarbamoyl)phenyl acetate

: 1542268-37-0
C₂₅H₃₁N₇O₅S

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / methanol / 5 h / 20 °C

2: sodium hydrogencarbonate / water; acetone / 2 h / 20 °C

3: bis-triphenylphosphine-palladium(II) chloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 95 °C / Inert atmosphere

4: sodium hydride / acetonitrile / 2 h / 20 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; sodium hydride; sodium hydrogencarbonate; potassium carbonate; N-ethyl-N,N-diisopropylamine; In methanol; water; N,N-dimethyl-formamide; acetone; acetonitrile;

Reference yield:

: 2345-34-8
4-acetyloxy-benzoic acid

: 1542268-37-0
C₂₅H₃₁N₇O₅S

Guidance literature:: Multi-step reaction with 6 steps

1: oxalyl dichloride / 4 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 3 h / 20 °C

3: potassium carbonate / methanol / 5 h / 20 °C

4: sodium hydrogencarbonate / water; acetone / 2 h / 20 °C

5: bis-triphenylphosphine-palladium(II) chloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 16 h / 95 °C / Inert atmosphere

6: sodium hydride / acetonitrile / 2 h / 20 °C / Inert atmosphere

With bis-triphenylphosphine-palladium(II) chloride; oxalyl dichloride; sodium hydride; sodium hydrogencarbonate; potassium carbonate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; acetone; acetonitrile;