C₃₅H₃₆N₄O₅

Base Information

Chemical Name:C₃₅H₃₆N₄O₅
CAS No.:1371592-95-8
Molecular Formula:C₃₅H₃₆N₄O₅
Molecular Weight:592.695
Hs Code.:

C<sub>35</sub>H<sub>36</sub>N<sub>4</sub>O<sub>5</sub>

Synonyms:C₃₅H₃₆N₄O₅

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Chemical Property of C₃₅H₃₆N₄O₅

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Technology Process of C₃₅H₃₆N₄O₅

There total 9 articles about C₃₅H₃₆N₄O₅ 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: 87.0%

: 13722-73-1
4-ethylpent-4-enoic acid

: 1371593-00-8
C₂₈H₂₆N₄O₄

: 1371592-95-8
C₃₅H₃₆N₄O₅

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 18h;
DOI:10.1021/ol300599p

Reference yield:

: C₂₂H₂₁NO

: 1371592-95-8
C₃₅H₃₆N₄O₅

Guidance literature:: Multi-step reaction with 7 steps

1: trichlorophosphate / N,N-dimethyl-formamide / 1.58 h / 0 - 35 °C

2: ammonium acetate / 1 h / Inert atmosphere; Reflux

3: lithium aluminium tetrahydride / tetrahydrofuran / 1.5 h / 0 °C / Reflux

4: 1,1'-carbonyldiimidazole / tetrahydrofuran; dichloromethane / 0 - 20 °C

5: acetic acid / tetrahydrofuran / 40 °C

6: triethylamine; p-toluenesulfonyl chloride / dichloromethane / 6 h / 0 - 20 °C

7: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 18 h / 20 °C

With dmap; lithium aluminium tetrahydride; ammonium acetate; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; p-toluenesulfonyl chloride; 1,1'-carbonyldiimidazole; trichlorophosphate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol300599p

Reference yield:

: 1371593-14-4
C₂₃H₁₉NO₂

: 1371592-95-8
C₃₅H₃₆N₄O₅

Guidance literature:: Multi-step reaction with 6 steps

1: ammonium acetate / 1 h / Inert atmosphere; Reflux

2: lithium aluminium tetrahydride / tetrahydrofuran / 1.5 h / 0 °C / Reflux

3: 1,1'-carbonyldiimidazole / tetrahydrofuran; dichloromethane / 0 - 20 °C

4: acetic acid / tetrahydrofuran / 40 °C

5: triethylamine; p-toluenesulfonyl chloride / dichloromethane / 6 h / 0 - 20 °C

6: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 18 h / 20 °C

With dmap; lithium aluminium tetrahydride; ammonium acetate; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; p-toluenesulfonyl chloride; 1,1'-carbonyldiimidazole; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ol300599p