C₄₃H₅₄N₆O₁₄

Base Information

Chemical Name:C₄₃H₅₄N₆O₁₄
CAS No.:1448861-58-2
Molecular Formula:C₄₃H₅₄N₆O₁₄
Molecular Weight:878.934
Hs Code.:

C<sub>43</sub>H<sub>54</sub>N<sub>6</sub>O<sub>14</sub>

Synonyms:C₄₃H₅₄N₆O₁₄

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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 C₄₃H₅₄N₆O₁₄

Chemical Property:

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Technology Process of C₄₃H₅₄N₆O₁₄

There total 15 articles about C₄₃H₅₄N₆O₁₄ 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: 75.0%

: 1448861-57-1
C₃₆H₄₉N₅O₁₂

: 96315-26-3
2-chloromethyloxazole-5-carboxylic acid,ethyl ester

: 1448861-58-2
C₄₃H₅₄N₆O₁₄

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 100 ℃; for 1.5h; Inert atmosphere;
DOI:10.1039/c3cc42489h

Reference yield:

: 1448861-54-8
C₄₂H₅₅BrN₂O₁₁

: 1448861-58-2
C₄₃H₅₄N₆O₁₄

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium azide / N,N-dimethyl-formamide / 2 h / 100 °C

2.1: trichlorophosphate / 0.25 h / 20 °C / Inert atmosphere

2.2: 12 h / 20 °C

3.1: magnesium dibromide / benzene / 24 h / 20 - 90 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 1.5 h / 100 °C / Inert atmosphere

With sodium azide; magnesium dibromide; potassium carbonate; trichlorophosphate; In N,N-dimethyl-formamide; benzene;
DOI:10.1039/c3cc42489h

Reference yield:

: 123-31-9,8027-02-9
hydroquinone

: 1448861-58-2
C₄₃H₅₄N₆O₁₄

Guidance literature:: Multi-step reaction with 13 steps

1.1: potassium hydroxide / ethanol / 12 h / 20 °C

2.1: nitric acid / acetic acid / 12 h / 50 °C / Cooling with ice

3.1: trifluoroacetic acid / dichloromethane / 48 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 72 h / 100 °C / Inert atmosphere

5.1: dmap / dichloromethane / 12 h / 0 - 20 °C

6.1: potassium hydroxide / ethanol; water

6.2: 12 h / 120 °C / Inert atmosphere

7.1: hydrogenchloride; tin(II) chloride dihdyrate / ethanol / 0.17 h / 90 °C

8.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 12 h / 90 °C

9.1: hydrogen bromide / dichloromethane; acetic acid / 12 h / 20 °C

10.1: sodium azide / N,N-dimethyl-formamide / 2 h / 100 °C

11.1: trichlorophosphate / 0.25 h / 20 °C / Inert atmosphere

11.2: 12 h / 20 °C

12.1: magnesium dibromide / benzene / 24 h / 20 - 90 °C

13.1: potassium carbonate / N,N-dimethyl-formamide / 1.5 h / 100 °C / Inert atmosphere

With hydrogenchloride; dmap; sodium azide; tin(II) chloride dihdyrate; hydrogen bromide; nitric acid; magnesium dibromide; potassium carbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; potassium hydroxide; trichlorophosphate; In ethanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide; acetonitrile; benzene;
DOI:10.1039/c3cc42489h