2',3'-anhydro-6'-N-benzyloxycarbonyl-4'',6''-O-cyclohexylidene-3'-epi-1,3,3''-tri-N-tosylkanamycin A

Base Information

Chemical Name:2',3'-anhydro-6'-N-benzyloxycarbonyl-4'',6''-O-cyclohexylidene-3'-epi-1,3,3''-tri-N-tosylkanamycin A
CAS No.:139978-74-8
Molecular Formula:C₅₃H₆₆N₄O₁₈S₃
Molecular Weight:1143.32
Hs Code.:

Synonyms:2',3'-anhydro-6'-N-benzyloxycarbonyl-4'',6''-O-cyclohexylidene-3'-epi-1,3,3''-tri-N-tosylkanamycin A

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Chemical Property of 2',3'-anhydro-6'-N-benzyloxycarbonyl-4'',6''-O-cyclohexylidene-3'-epi-1,3,3''-tri-N-tosylkanamycin A

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Technology Process of 2',3'-anhydro-6'-N-benzyloxycarbonyl-4'',6''-O-cyclohexylidene-3'-epi-1,3,3''-tri-N-tosylkanamycin A

There total 4 articles about 2',3'-anhydro-6'-N-benzyloxycarbonyl-4'',6''-O-cyclohexylidene-3'-epi-1,3,3''-tri-N-tosylkanamycin A 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: 89.0%

: 105507-33-3
3'-O-benzylsulfonyl-6'-N,4'-O-carbonyl-4'',6''-O-cyclohexylidene-1,3,3''-tri-N-tosylkanamycin A

: 20194-18-7
sodium phenyl-methanolate

: 139978-74-8
2',3'-anhydro-6'-N-benzyloxycarbonyl-4'',6''-O-cyclohexylidene-3'-epi-1,3,3''-tri-N-tosylkanamycin A

Guidance literature:: In benzyl alcohol; at 45 ℃; for 0.00833333h;
DOI:10.1016/0008-6215(92)84101-W

Reference yield:

: 76550-53-3
6'-N,4'-O-carbonyl-4'',6''-O-cyclohexylidene-1,3,3''-tri-N-tosylkanamycin A

: 139978-74-8
2',3'-anhydro-6'-N-benzyloxycarbonyl-4'',6''-O-cyclohexylidene-3'-epi-1,3,3''-tri-N-tosylkanamycin A

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / pyridine, 5percent NaHCO₃ / dimethylsulfoxide; H₂O / Ambient temperature

2: 88 mg / pyridine / 0.17 h / 0 - 5 °C

3: 88 percent / Zemplen deacetylation

4: 89 percent / phenylmethanol / 0.01 h / 45 °C

With pyridine; sodium hydrogencarbonate; In water; dimethyl sulfoxide; benzyl alcohol;
DOI:10.1016/0008-6215(92)84101-W

Reference yield:

: 106996-47-8
2',2''-di-O-acetyl-6'-N,4'-O-carbonyl-4'',6''-O-cyclohexylidene-1,3,3''-tri-N-tosyl-kanamycin A

: 139978-74-8
2',3'-anhydro-6'-N-benzyloxycarbonyl-4'',6''-O-cyclohexylidene-3'-epi-1,3,3''-tri-N-tosylkanamycin A

Guidance literature:: Multi-step reaction with 3 steps

1: 88 mg / pyridine / 0.17 h / 0 - 5 °C

2: 88 percent / Zemplen deacetylation

3: 89 percent / phenylmethanol / 0.01 h / 45 °C

With pyridine; In benzyl alcohol;
DOI:10.1016/0008-6215(92)84101-W