N^ε-(tert-butyloxycarbonyl)-(S)-lysinyl-5-amino-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester

Base Information

• Chemical Name: N^ε-(tert-butyloxycarbonyl)-(S)-lysinyl-5-amino-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester
• CAS No.: 849599-79-7
• Molecular Formula: C₂₄H₃₅N₅O₆
• Molecular Weight: 489.572

Synonyms:N^ε-(tert-butyloxycarbonyl)-(S)-lysinyl-5-amino-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester

Chemical Property of N^ε-(tert-butyloxycarbonyl)-(S)-lysinyl-5-amino-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester

Chemical Property:

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Technology Process of N^ε-(tert-butyloxycarbonyl)-(S)-lysinyl-5-amino-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester

There total 4 articles about N^ε-(tert-butyloxycarbonyl)-(S)-lysinyl-5-amino-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester 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: 74.0%

5-(N2-benzyloxycarbonyl-N6-tert-butyloxycarbonyl-(S)-lysyl-amino)-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester (849599-77-5) → Nε-(tert-butyloxycarbonyl)-(S)-lysinyl-5-amino-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester (849599-79-7)

Guidance literature:

With hydrogen; palladium on activated charcoal; In methanol;

DOI:10.1021/ja045558b

Reference yield:

5-amino-2-(p-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester (625386-12-1) → Nε-(tert-butyloxycarbonyl)-(S)-lysinyl-5-amino-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester (849599-79-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 76 percent / HCTU; 6-chloro-1-hydroxy-1H-benzotriazole; 2,6-lutidine / CH₂Cl₂; dimethylformamide / 3.5 h

2: 70 percent / hydrogen / palladium on carbon / methanol / 16 h

With 2,6-dimethylpyridine; 6-chloro-3-((dimethylamino)(dimethyliminio)methyl)-1H-benzo[d][1,2,3]triazol-3-ium-1-olatehexafluorophosphate(V); hydrogen; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1021/jo061918x

Reference yield:

Z-Lys(Boc)-OH (2389-60-8) → Nε-(tert-butyloxycarbonyl)-(S)-lysinyl-5-amino-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester (849599-79-7)

Guidance literature:

Multi-step reaction with 2 steps

1.1: HCTU; Cl-HOBt; 2,6-lutidine / CH₂Cl₂; dimethylformamide / 0.17 h / 0 °C

1.2: 60 percent / CH₂Cl₂; dimethylformamide

2.1: 74 percent / H₂ / Pd/C / methanol

With 2,6-dimethylpyridine; 6-chloro-3-((dimethylamino)(dimethyliminio)methyl)-1H-benzo[d][1,2,3]triazol-3-ium-1-olatehexafluorophosphate(V); hydrogen; 6-chloro-1-hydroxybenzotriazole; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.1021/ja045558b

upstream raw materials:

5-(N²-benzyloxycarbonyl-N⁶-tert-butyloxycarbonyl-(S)-lysyl-amino)-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester

5-amino-2-(p-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester

2-(4-methoxybenzyl)-5-nitro-2H-pyrazole-3-carboxylic acid methyl ester

Z-Lys(Boc)-OH

Downstream raw materials:

C₅₄H₇₈N₁₀O₁₅

N^ε-(tert-butyloxycarbonyl)-(S)-lysinyl-N^ε-(tert-butyloxycarbonyl)-(S)-lysinyl-5-amino-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester

5-{5-[2-[2-(2-methoxy-ethoxy)-ethoxy]-acetylamino]-2-(4-methoxybenzyl)-2H-pyrazole-3-cabonyl-(S)-phenylalanyl-N⁶-tert-butyloxycarbonyl-(S)-lysyl-amino}-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester

5-{5-[2-[2-(2-methoxy-ethoxy)-ethoxy]-acetylamino]-2-(4-methoxybenzyl)-2H-pyrazole-3-cabonyl-(S)-alanyl-N⁶-tert-butyloxycarbonyl-(S)-lysyl-amino}-2-(4-methoxybenzyl)-2H-pyrazole-3-carboxylic acid methyl ester

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