C₃₆H₄₁ClFN₃O₆

Base Information

Chemical Name:C₃₆H₄₁ClFN₃O₆
CAS No.:1268843-77-1
Molecular Formula:C₃₆H₄₁ClFN₃O₆
Molecular Weight:666.189
Hs Code.:

C<sub>36</sub>H<sub>41</sub>ClFN<sub>3</sub>O<sub>6</sub>

Synonyms:C₃₆H₄₁ClFN₃O₆

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Chemical Property of C₃₆H₄₁ClFN₃O₆

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Technology Process of C₃₆H₄₁ClFN₃O₆

There total 5 articles about C₃₆H₄₁ClFN₃O₆ 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:

: 78607-32-6
3-amino-2,5-dichloropyridine

: 1268843-77-1
C₃₆H₄₁ClFN₃O₆

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-ethyl-N,N-diisopropylamine; tetrabutylammomium bromide / 1,4-di(diphenylphosphino)-butane; palladium diacetate / N,N-dimethyl-formamide / 30 h / 140 °C

2.1: trifluoroacetic acid / dichloromethane / 0.25 h / 20 °C

2.2: 1.5 h / 40 °C

2.3: 1.7percent palladium-fibroin / 18 h / 20 °C

3.1: potassium tert-butylate / tetrahydrofuran / 0.5 h

4.1: lithium hexamethyldisilazane / hexane; tetrahydrofuran / 0.67 h / -20 °C

4.2: 2 h / -20 - 0 °C

5.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / 1 h / -78 - 0 °C

5.3: 5 h / 20 °C

With trimethylsilyl trifluoromethanesulfonate; potassium tert-butylate; tetrabutylammomium bromide; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; lithium hexamethyldisilazane; palladium diacetate; 1,4-di(diphenylphosphino)-butane; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide; 1.1: Heck Reaction;

Reference yield:

: 1268843-71-5
benzyl 2'-{[(1R)-3-tert-butoxy-1-methyl-3-oxopropyl]oxy}-3-fluorobiphenyl-4-carboxylate

: 1268843-77-1
C₃₆H₄₁ClFN₃O₆

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen / palladium 10% on activated carbon / ethanol / 7 h / 20 °C

2.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / 1 h / -78 - 0 °C

2.3: 5 h / 20 °C

With trimethylsilyl trifluoromethanesulfonate; hydrogen; palladium 10% on activated carbon; In ethanol; dichloromethane;

Reference yield:

: 1268844-22-9
C₂₄H₂₁FO₅

: 1268843-77-1
C₃₆H₄₁ClFN₃O₆

Guidance literature:: Multi-step reaction with 3 steps

1.1: diisopropyl-carbodiimide / copper(l) chloride / 96 h / 20 °C / Darkness

1.2: 4.5 h / 60 °C

2.1: hydrogen / palladium 10% on activated carbon / ethanol / 7 h / 20 °C

3.1: trimethylsilyl trifluoromethanesulfonate / dichloromethane / 1 h / -78 - 0 °C

3.3: 5 h / 20 °C

With trimethylsilyl trifluoromethanesulfonate; hydrogen; diisopropyl-carbodiimide; palladium 10% on activated carbon; copper(l) chloride; In ethanol; dichloromethane;