1,2',6'-tri-N-benzyloxycarbonyl-2''-N-formimidoylistamycin A hydrochloride

Base Information

Chemical Name:1,2',6'-tri-N-benzyloxycarbonyl-2''-N-formimidoylistamycin A hydrochloride
CAS No.:81155-03-5
Molecular Formula:C₄₂H₅₄N₆O₁₁*ClH
Molecular Weight:855.385
Hs Code.:

Synonyms:1,2',6'-tri-N-benzyloxycarbonyl-2''-N-formimidoylistamycin A hydrochloride

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Chemical Property of 1,2',6'-tri-N-benzyloxycarbonyl-2''-N-formimidoylistamycin A hydrochloride

Chemical Property:

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Technology Process of 1,2',6'-tri-N-benzyloxycarbonyl-2''-N-formimidoylistamycin A hydrochloride

There total 3 articles about 1,2',6'-tri-N-benzyloxycarbonyl-2''-N-formimidoylistamycin A hydrochloride 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: 54.0%

: 60099-09-4
methanimidic acid phenylmethyl ester hydrochloride

: 81155-15-9
1,2',6'-tri-N-benzyloxycarbonylistamycin A trifluoroacetat

: 81155-03-5
1,2',6'-tri-N-benzyloxycarbonyl-2''-N-formimidoylistamycin A hydrochloride

Guidance literature:: In methanol; for 1h;
DOI:10.1016/0008-6215(82)84028-7

Reference yield:

: 81155-13-7
1,2',6'-tri-N-benzyloxycarbonyl-2''-N-tert-butoxycarbonylistamycin A

: 81155-03-5
1,2',6'-tri-N-benzyloxycarbonyl-2''-N-formimidoylistamycin A hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 375 mg / 90percent aq. CF₃COOH / 0.75 h / Ambient temperature

2: 54 percent / methanol / 1 h

With trifluoroacetic acid; In methanol;
DOI:10.1016/0008-6215(82)84028-7

Reference yield:

: 73113-81-2
1,2',6'-tri-N-benzyloxycarbonylistamycin A₀

: 81155-03-5
1,2',6'-tri-N-benzyloxycarbonyl-2''-N-formimidoylistamycin A hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: 39 percent / Et₃N / dioxane / 4.5 h / 60 °C

2: 375 mg / 90percent aq. CF₃COOH / 0.75 h / Ambient temperature

3: 54 percent / methanol / 1 h

With triethylamine; trifluoroacetic acid; In 1,4-dioxane; methanol;
DOI:10.1016/0008-6215(82)84028-7