C₂₆H₃₅FN₁₀O₂

Base Information

Chemical Name:C₂₆H₃₅FN₁₀O₂
CAS No.:1309833-24-6
Molecular Formula:C₂₆H₃₅FN₁₀O₂
Molecular Weight:538.628
Hs Code.:

C<sub>26</sub>H<sub>35</sub>FN<sub>10</sub>O<sub>2</sub>

Synonyms:C₂₆H₃₅FN₁₀O₂

Suppliers and Price of C₂₆H₃₅FN₁₀O₂

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₂₆H₃₅FN₁₀O₂

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₆H₃₅FN₁₀O₂

There total 17 articles about C₂₆H₃₅FN₁₀O₂ 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: 53.0%

: 1309831-16-0
1-(5-amino-2-cyclopropyl-4-fluorophenyl)-4-methyl-1H-tetrazol-5(4H)-one

: 1309831-09-1
5-aminocarbonyl-2-chloro-N₄-(1,2,2,6,6-pentamethylpiperidin-4-yl)-4-pyrimidineamine hydrochloride

: 1309833-24-6
C₂₆H₃₅FN₁₀O₂

Guidance literature:: 1-(5-amino-2-cyclopropyl-4-fluorophenyl)-4-methyl-1H-tetrazol-5(4H)-one; 5-aminocarbonyl-2-chloro-N₄-(1,2,2,6,6-pentamethylpiperidin-4-yl)-4-pyrimidineamine hydrochloride; With toluene-4-sulfonic acid; In isopropyl alcohol; at 100 ℃; Sealed vial;

With sodium hydroxide; In ethyl acetate;

Reference yield:

: 1003-98-1
2-bromo-4-fluoroaniline

: 1309833-24-6
C₂₆H₃₅FN₁₀O₂

Guidance literature:: Multi-step reaction with 7 steps

1: nitric acid; sulfuric acid / 1.08 h / -20 - -15 °C

2: toluene / 2.5 h / 80 °C / Inert atmosphere

3: trimethylsilylazide / 80 °C / Inert atmosphere

4: potassium carbonate / N,N-dimethyl-formamide / -78 - 20 °C / Inert atmosphere

5: caesium carbonate / tricyclohexylphosphine; palladium diacetate / toluene; water / 100 °C / Inert atmosphere

6: hydrogenchloride; tin(II) chloride dihdyrate / ethanol; water / 80 °C

7: toluene-4-sulfonic acid / isopropyl alcohol / 100 °C / Sealed vial

With hydrogenchloride; tin(II) chloride dihdyrate; trimethylsilylazide; sulfuric acid; nitric acid; potassium carbonate; caesium carbonate; toluene-4-sulfonic acid; palladium diacetate; tricyclohexylphosphine; In ethanol; water; N,N-dimethyl-formamide; isopropyl alcohol; toluene; 5: Suzuki Coupling;

Reference yield:

: 346433-97-4
2-bromo-4-fluoro-5-nitrophenylamine

: 1309833-24-6
C₂₆H₃₅FN₁₀O₂

Guidance literature:: Multi-step reaction with 6 steps

1: toluene / 2.5 h / 80 °C / Inert atmosphere

2: trimethylsilylazide / 80 °C / Inert atmosphere

3: potassium carbonate / N,N-dimethyl-formamide / -78 - 20 °C / Inert atmosphere

4: caesium carbonate / tricyclohexylphosphine; palladium diacetate / toluene; water / 100 °C / Inert atmosphere

5: hydrogenchloride; tin(II) chloride dihdyrate / ethanol; water / 80 °C

6: toluene-4-sulfonic acid / isopropyl alcohol / 100 °C / Sealed vial

With hydrogenchloride; tin(II) chloride dihdyrate; trimethylsilylazide; potassium carbonate; caesium carbonate; toluene-4-sulfonic acid; palladium diacetate; tricyclohexylphosphine; In ethanol; water; N,N-dimethyl-formamide; isopropyl alcohol; toluene; 4: Suzuki Coupling;