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C28H37N5O4

Base Information Edit
C<sub>28</sub>H<sub>37</sub>N<sub>5</sub>O<sub>4</sub>

Synonyms:C28H37N5O4

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C28H37N5O4 Edit
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Technology Process of C28H37N5O4

There total 5 articles about C28H37N5O4 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:
Guidance literature:
C28H37N5O5; With acetic anhydride; acetic acid; for 0.5h;
With palladium 10% on activated carbon; hydrogen; for 12h; under 2585.81 - 2844.39 Torr;
DOI:10.1016/j.bioorg.2020.103856
Guidance literature:
Multi-step reaction with 5 steps
1.1: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.17 h
1.2: 16 h / 20 °C
2.1: hydrogenchloride / methanol; water / 3 h / 0 - 20 °C
3.1: 1-hydroxy-7-aza-benzotriazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 0.17 h
3.2: 16 h / 20 °C
4.1: hydroxylamine hydrochloride / methanol / 0.17 h
4.2: 18 h
5.1: acetic acid; acetic anhydride / 0.5 h
5.2: 12 h / 2585.81 - 2844.39 Torr
With hydrogenchloride; 1-hydroxy-7-aza-benzotriazole; hydroxylamine hydrochloride; acetic anhydride; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bioorg.2020.103856
Guidance literature:
Multi-step reaction with 2 steps
1.1: hydroxylamine hydrochloride / methanol / 0.17 h
1.2: 18 h
2.1: acetic acid; acetic anhydride / 0.5 h
2.2: 12 h / 2585.81 - 2844.39 Torr
With hydroxylamine hydrochloride; acetic anhydride; acetic acid; In methanol;
DOI:10.1016/j.bioorg.2020.103856
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