C₃₆H₄₃N₃O₅

Base Information

Chemical Name:C₃₆H₄₃N₃O₅
CAS No.:1447825-61-7
Molecular Formula:C₃₆H₄₃N₃O₅
Molecular Weight:597.755
Hs Code.:

C<sub>36</sub>H<sub>43</sub>N<sub>3</sub>O<sub>5</sub>

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 C₃₆H₄₃N₃O₅

Chemical Property:

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Technology Process of C₃₆H₄₃N₃O₅

There total 17 articles about C₃₆H₄₃N₃O₅ 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:

: 1447825-64-0
C₂₅H₃₇N₃O₄

: 2243-83-6
2-naphthaloyl chloride

: 1447825-61-7
C₃₆H₄₃N₃O₅

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1021/jm400542h

Reference yield:

: C₃₅H₄₉NO₂SSi

: 1447825-61-7
C₃₆H₄₃N₃O₅

Guidance literature:: Multi-step reaction with 12 steps

1: hydrogenchloride / methanol; ethyl acetate / 5 h / 20 °C

2: sodium carbonate / tetrahydrofuran; water / 12 h / 20 °C

3: Dess-Martin periodane / dichloromethane / 0.5 h / 20 °C

4: 2-methyl-but-2-ene; sodium dihydrogenphosphate dihydrate; sodium chlorite / tetrahydrofuran; tert-butyl alcohol; water / 14 h / 20 °C

5: triethylamine; diphenyl phosphoryl azide / dichloromethane / 17.33 h / 0 - 20 °C

6: 29 h / Reflux

7: potassium carbonate / methanol / 14 h / 20 °C

8: triethylamine / dichloromethane / 3 h / 0 - 20 °C

9: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

10: triethylamine / dichloromethane / 19 h / 0 - 20 °C

11: trifluoroacetic acid; palladium on activated charcoal; hydrogen / tetrahydrofuran / 1 h / 0 °C

12: triethylamine / dichloromethane / 1 h / 0 °C

With hydrogenchloride; sodium chlorite; sodium dihydrogenphosphate dihydrate; 2-methyl-but-2-ene; diphenyl phosphoryl azide; palladium on activated charcoal; hydrogen; sodium carbonate; potassium carbonate; Dess-Martin periodane; triethylamine; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; tert-butyl alcohol; 3: |Dess-Martin Oxidation;
DOI:10.1021/jm400542h

Reference yield:

: 692778-40-8
(3S,4R)-3-((S)-sec-butyl)-4-oxooxetane-2-carboxylic acid

: 1447825-61-7
C₃₆H₄₃N₃O₅

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 1 h / 0 °C

2: triethylamine / dichloromethane / 19 h / 0 - 20 °C

3: trifluoroacetic acid; palladium on activated charcoal; hydrogen / tetrahydrofuran / 1 h / 0 °C

4: triethylamine / dichloromethane / 1 h / 0 °C

With palladium on activated charcoal; hydrogen; triethylamine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm400542h