4'',6''-O-Cyclohexylidene-3'-deoxy-3'-fluoro-6'-N-methoxycarbonyl-1,3,2',3''-tetra-N-tosylkanamycin B

Base Information

Chemical Name:4'',6''-O-Cyclohexylidene-3'-deoxy-3'-fluoro-6'-N-methoxycarbonyl-1,3,2',3''-tetra-N-tosylkanamycin B
CAS No.:100343-24-6
Molecular Formula:C₅₄H₇₀FN₅O₁₉S₄
Molecular Weight:1240.43
Hs Code.:

Synonyms:4'',6''-O-Cyclohexylidene-3'-deoxy-3'-fluoro-6'-N-methoxycarbonyl-1,3,2',3''-tetra-N-tosylkanamycin B

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Chemical Property of 4'',6''-O-Cyclohexylidene-3'-deoxy-3'-fluoro-6'-N-methoxycarbonyl-1,3,2',3''-tetra-N-tosylkanamycin B

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Technology Process of 4'',6''-O-Cyclohexylidene-3'-deoxy-3'-fluoro-6'-N-methoxycarbonyl-1,3,2',3''-tetra-N-tosylkanamycin B

There total 4 articles about 4'',6''-O-Cyclohexylidene-3'-deoxy-3'-fluoro-6'-N-methoxycarbonyl-1,3,2',3''-tetra-N-tosylkanamycin B 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: 49.0%

: 105507-32-2
4'',6''-O-Cyclohexylidene-2'-deamino-3'-deoxy-3'-epi-6'-N-methoxycarbonyl-1,3,3''-tri-N-tosyl-2',3'-(N-tosylepimino)kanamycin B

: 100343-24-6
4'',6''-O-Cyclohexylidene-3'-deoxy-3'-fluoro-6'-N-methoxycarbonyl-1,3,2',3''-tetra-N-tosylkanamycin B

Guidance literature:: With potassium hydrogen bifluoride; In N,N-dimethyl-formamide; at 150 ℃; for 2h; Further byproducts given;
DOI:10.1016/S0008-6215(00)90515-9

Reference yield:

: 100343-21-3
2''-O-Acetyl-6'-N,4'-O-carbonyl-4'',6''-O-cyclohexylidene-1,3,2',3''-tetra-N-tosylkanamycin B

: 100343-24-6
4'',6''-O-Cyclohexylidene-3'-deoxy-3'-fluoro-6'-N-methoxycarbonyl-1,3,2',3''-tetra-N-tosylkanamycin B

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / pyridine / 4.5 h / -20 °C

2: 92 percent / 0.5 M NaOH / methanol / 4 h / Ambient temperature

3: 49 percent / KHF₂ / dimethylformamide / 2 h / 150 °C

With pyridine; sodium hydroxide; potassium hydrogen bifluoride; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(00)90515-9

Reference yield:

: 100343-22-4
2''-O-Acetyl-3'-O-benzylsulfonyl-6'-N,4'-O-carbonyl-4'',6''-O-cyclohexylidene-1,3,2',3''-tetra-N-tosylkanamycin B

: 100343-24-6
4'',6''-O-Cyclohexylidene-3'-deoxy-3'-fluoro-6'-N-methoxycarbonyl-1,3,2',3''-tetra-N-tosylkanamycin B

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / 0.5 M NaOH / methanol / 4 h / Ambient temperature

2: 49 percent / KHF₂ / dimethylformamide / 2 h / 150 °C

With sodium hydroxide; potassium hydrogen bifluoride; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(00)90515-9