N¹-benzyloxycarbonyl-N⁸-(N^α-t-butoxycarbonyl-N^g-tosyl-N^α-methylarginyl-D-leucyl)-1,8-octanediamine

Base Information

• Chemical Name: N¹-benzyloxycarbonyl-N⁸-(N^α-t-butoxycarbonyl-N^g-tosyl-N^α-methylarginyl-D-leucyl)-1,8-octanediamine
• CAS No.: 212716-36-4
• Molecular Formula: C₄₁H₆₅N₇O₈S
• Molecular Weight: 816.075

Synonyms:N¹-benzyloxycarbonyl-N⁸-(N^α-t-butoxycarbonyl-N^g-tosyl-N^α-methylarginyl-D-leucyl)-1,8-octanediamine

Chemical Property of N¹-benzyloxycarbonyl-N⁸-(N^α-t-butoxycarbonyl-N^g-tosyl-N^α-methylarginyl-D-leucyl)-1,8-octanediamine

Chemical Property:

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Technology Process of N¹-benzyloxycarbonyl-N⁸-(N^α-t-butoxycarbonyl-N^g-tosyl-N^α-methylarginyl-D-leucyl)-1,8-octanediamine

There total 4 articles about N¹-benzyloxycarbonyl-N⁸-(N^α-t-butoxycarbonyl-N^g-tosyl-N^α-methylarginyl-D-leucyl)-1,8-octanediamine 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: 93.0%

Boc-N-Me-Arg(Tos)-OH (108695-16-5,136642-84-7) + N1-benzyloxycarbonyl-N8-D-leucyl-1,8-octanediamine (175216-23-6) → N1-benzyloxycarbonyl-N8-(Nα-t-butoxycarbonyl-Ng-tosyl-Nα-methylarginyl-D-leucyl)-1,8-octanediamine (212716-36-4)

Guidance literature:

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; 1.) 0 deg C, 10 min, 2.) room temperature, overnight;

DOI:10.1016/S0968-0896(98)00031-5

Reference yield:

N-Boc-D-Leu (16937-99-8,53296-34-7) → N1-benzyloxycarbonyl-N8-(Nα-t-butoxycarbonyl-Ng-tosyl-Nα-methylarginyl-D-leucyl)-1,8-octanediamine (212716-36-4)

Guidance literature:

Multi-step reaction with 3 steps

1: 97.8 percent / DCC, TEA, HOBt / dimethylformamide / Ambient temperature

2: 1.) TFA, 2.) NaHCO₃ / 1.) CH₂Cl₂, 2 h, 2.) AcOEt

3: 93 percent / HOBt, EDC*HCl / dimethylformamide / 1.) 0 deg C, 10 min, 2.) room temperature, overnight

With TEA; sodium hydrogencarbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dicyclohexyl-carbodiimide; trifluoroacetic acid; In N,N-dimethyl-formamide;

DOI:10.1016/S0968-0896(98)00031-5

Reference yield:

N1-benzyloxycarbonyl-N8-(t-butoxycarbonyl-D-leucyl)-1,8-octanediamine (175216-22-5) → N1-benzyloxycarbonyl-N8-(Nα-t-butoxycarbonyl-Ng-tosyl-Nα-methylarginyl-D-leucyl)-1,8-octanediamine (212716-36-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 1.) TFA, 2.) NaHCO₃ / 1.) CH₂Cl₂, 2 h, 2.) AcOEt

2: 93 percent / HOBt, EDC*HCl / dimethylformamide / 1.) 0 deg C, 10 min, 2.) room temperature, overnight

With sodium hydrogencarbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In N,N-dimethyl-formamide;

DOI:10.1016/S0968-0896(98)00031-5

upstream raw materials:

Boc-N-Me-Arg(Tos)-OH

N¹-benzyloxycarbonyl-N⁸-D-leucyl-1,8-octanediamine

N-Boc-D-Leu

N¹-benzyloxycarbonyl-N⁸-(t-butoxycarbonyl-D-leucyl)-1,8-octanediamine

Downstream raw materials:

N¹-(4-nitrobenzo-6-oxa-5,7-diazolyl)-N⁸-(N^α-t-butoxycarbonyl-N^g-tosylarginyl-N^g-tosyl-N^α-methylarginyl-D-leucyl)-1,8-octanediamine

N¹-benzyloxycarbonyl-N⁸-(N^α-t-butoxycarbonyl-N^g-tosylarginyl-N^α-methyl-N^g-tosylarginyl-D-leucyl)-1,8-octanediamine

N¹-benzyloxycarbonyl-N⁸-(N^α-methyl-N^g-tosylarginyl-D-leucyl)-1,8-octanediamine

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