C₄₄H₆₁FN₆O₆

Base Information

Chemical Name:C₄₄H₆₁FN₆O₆
CAS No.:1246246-97-8
Molecular Formula:C₄₄H₆₁FN₆O₆
Molecular Weight:789.003
Hs Code.:

C<sub>44</sub>H<sub>61</sub>FN<sub>6</sub>O<sub>6</sub>

Synonyms:C₄₄H₆₁FN₆O₆

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Chemical Property of C₄₄H₆₁FN₆O₆

Chemical Property:

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Technology Process of C₄₄H₆₁FN₆O₆

There total 6 articles about C₄₄H₆₁FN₆O₆ 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:

: 403-24-7
2-fluoro-4-nitrobenzoic acid

: 1246246-97-8
C₄₄H₆₁FN₆O₆

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; pivaloyl chloride / dichloromethane / 0.25 h / 20 °C / Cooling with ice

1.2: 2 h / 20 °C / Cooling with ice

2.1: hydrogen / palladium 10% on activated carbon / methanol / 1 h / 20 °C

3.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 20 °C

3.2: 1 h / 20 °C

With hydrogen; pivaloyl chloride; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; palladium 10% on activated carbon; In methanol; dichloromethane;

Reference yield:

: 123183-72-2
N-(tert-butyl)oxycarbonyl-N,N’-trimethyl-1,3-diaminopropane

: 1246246-97-8
C₄₄H₆₁FN₆O₆

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; pivaloyl chloride / dichloromethane / 0.25 h / 20 °C / Cooling with ice

1.2: 2 h / 20 °C / Cooling with ice

2.1: hydrogen / palladium 10% on activated carbon / methanol / 1 h / 20 °C

3.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 20 °C

3.2: 1 h / 20 °C

With hydrogen; pivaloyl chloride; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; palladium 10% on activated carbon; In methanol; dichloromethane;

Reference yield:

: 1246246-94-5
tert-Butyl (3-{[(2-fluoro-4-nitrophenyl)carbonyl](methyl)amino}propyl)methylcarbamate

: 1246246-97-8
C₄₄H₆₁FN₆O₆

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen / palladium 10% on activated carbon / methanol / 1 h / 20 °C

2.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 20 °C

2.2: 1 h / 20 °C

With hydrogen; sodium tris(acetoxy)borohydride; acetic acid; palladium 10% on activated carbon; In methanol; dichloromethane;