C₃₀H₃₀FN₃O₄S

Base Information

Chemical Name:C₃₀H₃₀FN₃O₄S
CAS No.:1202077-71-1
Molecular Formula:C₃₀H₃₀FN₃O₄S
Molecular Weight:547.65
Hs Code.:

C<sub>30</sub>H<sub>30</sub>FN<sub>3</sub>O<sub>4</sub>S

Synonyms:

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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 C₃₀H₃₀FN₃O₄S

Chemical Property:

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Technology Process of C₃₀H₃₀FN₃O₄S

There total 5 articles about C₃₀H₃₀FN₃O₄S 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:

: 1202075-59-9
3-fluoro-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridin-2-yl)benzaldehyde

: 1202077-71-1
C₃₀H₃₀FN₃O₄S

Guidance literature:: Multi-step reaction with 6 steps

1.1: tetrahydrofuran / 0.5 h / 0 °C

2.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 0 °C

3.1: caesium carbonate / N,N-dimethyl-formamide / 1 h / 20 °C

3.2: 1.5 h / 35 °C

4.1: hydrogenchloride; water / 1 h / 120 °C

5.1: triethylamine / tetrahydrofuran; water / 18 h / 20 °C

6.1: Chiralpak AD-H / liquid carbon dioxide; ethanol / Resolution of racemate

With hydrogenchloride; potassium tert-butylate; water; caesium carbonate; triethylamine; In tetrahydrofuran; ethanol; liquid carbon dioxide; water; N,N-dimethyl-formamide; 1.1: Peterson olefination / 2.1: Peterson olefination;
DOI:10.1016/j.bmcl.2011.12.073

Reference yield:

: C₂₆H₂₇FN₂OSSi

: 1202077-71-1
C₃₀H₃₀FN₃O₄S

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 0 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 1 h / 20 °C

2.2: 1.5 h / 35 °C

3.1: hydrogenchloride; water / 1 h / 120 °C

4.1: triethylamine / tetrahydrofuran; water / 18 h / 20 °C

5.1: Chiralpak AD-H / liquid carbon dioxide; ethanol / Resolution of racemate

With hydrogenchloride; potassium tert-butylate; water; caesium carbonate; triethylamine; In tetrahydrofuran; ethanol; liquid carbon dioxide; water; N,N-dimethyl-formamide; 1.1: Peterson olefination;
DOI:10.1016/j.bmcl.2011.12.073

Reference yield:

: 1202076-81-0
C₃₂H₃₂FN₃O₅S

: 1202077-71-1
C₃₀H₃₀FN₃O₄S

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride; water / 1 h / 120 °C

2: triethylamine / tetrahydrofuran; water / 18 h / 20 °C

3: Chiralpak AD-H / liquid carbon dioxide; ethanol / Resolution of racemate

With hydrogenchloride; water; triethylamine; In tetrahydrofuran; ethanol; liquid carbon dioxide; water;
DOI:10.1016/j.bmcl.2011.12.073