7-aminoaziridinomitosene

Base Information

Chemical Name:7-aminoaziridinomitosene
CAS No.:103422-25-9
Molecular Formula:C₁₄H₁₄N₄O₄
Molecular Weight:302.29
Hs Code.:

Synonyms:7-aminoaziridinomitosene

Suppliers and Price of 7-aminoaziridinomitosene

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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 7-aminoaziridinomitosene

Chemical Property:

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Technology Process of 7-aminoaziridinomitosene

There total 2 articles about 7-aminoaziridinomitosene 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: 30.0%

: 50-07-7
mitomycin C

: 99745-88-7,78655-54-6
trans-1-hydroxy-2,7-diaminomitosene

: 98462-75-0,78655-54-6
2β,7-Diamino-1β-hydroxymitosene

: 103422-25-9
7-aminoaziridinomitosene

Guidance literature:: In methanol; for 0.0833333h; at -1.00 V, Pt electrode vs. SCE, supporting electrolyte: 0.1 M NaClO₄;
DOI:10.1021/jo00015a016

Reference yield:

: 4055-39-4
mitomycin A

: 103422-25-9
7-aminoaziridinomitosene

Guidance literature:: Multi-step reaction with 2 steps

1: 55 percent / H₂ / PtO₂ / ethyl acetate / 2 h

2: 20 percent / methanolic NH₃ / dimethylformamide / 2 h / Ambient temperature

With ammonia; hydrogen; platinum(IV) oxide; In ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/jm00160a012

Reference yield: 20.0%

: 144-55-8
sodium hydrogencarbonate

: 103422-25-9
7-aminoaziridinomitosene

: 1207530-65-1
C₁₅H₁₄N₄O₆

: 98462-75-0,78655-54-6
2β,7-Diamino-1β-hydroxymitosene

Guidance literature:: 7-aminoaziridinomitosene; With sodium hydrogencarbonate; In water; acetonitrile; at 20 ℃; for 5h;

sodium hydrogencarbonate; With tert-butyldicarbonate; In methanol; water; acetonitrile; at 20 ℃; for 24h; Further stages;
DOI:10.1016/j.bmcl.2009.11.046