N^α-tert-butoxycarbonyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine methyl ester

Base Information

• Chemical Name: N^α-tert-butoxycarbonyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine methyl ester
• CAS No.: 522644-19-5
• Molecular Formula: C₆₆H₈₇N₁₅O₁₅
• Molecular Weight: 1330.51

Synonyms:N^α-tert-butoxycarbonyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine methyl ester

Chemical Property of N^α-tert-butoxycarbonyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

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Technology Process of N^α-tert-butoxycarbonyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine methyl ester

There total 6 articles about N^α-tert-butoxycarbonyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine 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: 82.0%

Nα-tert-butoxycarbonyl-Nε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine (522644-16-2) + 3-[(S)-2-{3-[(S)-2-Amino-6-(1-benzyloxy-2-oxo-1,2-dihydro-pyrimidin-4-ylamino)-hexanoylamino]-propionylamino}-6-(1-benzyloxy-2-oxo-1,2-dihydro-pyrimidin-4-ylamino)-hexanoylamino]-propionic acid methyl ester; compound with trifluoro-acetic acid → Nα-tert-butoxycarbonyl-Nε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl Nε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl-Nε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine methyl ester (522644-19-5)

Guidance literature:

With 4-methyl-morpholine; WSC*HCl; benzotriazol-1-ol; In dichloromethane; N,N-dimethyl-formamide; at 0 - 20 ℃; for 73h;

DOI:10.3987/COM-02-S(M)34

Reference yield:

N-α-(tert-butoxycarbonyl)-L-lysine methyl ester (55757-60-3) → Nα-tert-butoxycarbonyl-Nε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl Nε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl-Nε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine methyl ester (522644-19-5)

Guidance literature:

Multi-step reaction with 5 steps

1: 83 percent / CH₂Cl₂ / 144 h / 40 °C

2: 98 percent / aq. NaOH / methanol / 3 h / 20 °C

3: 87 percent / N-methylmorpholine; HOBt*H₂O; WSC*HCl / CH₂Cl₂ / 50 h / 0 - 20 °C

4: 85 percent / aq. NaOH / methanol / 20 °C

5: 82 percent / N-methylmorpholine; HOBt*H₂O; WSC*HCl / dimethylformamide; CH₂Cl₂ / 73 h / 0 - 20 °C

With 4-methyl-morpholine; sodium hydroxide; WSC*HCl; benzotriazol-1-ol; In methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.3987/COM-02-S(M)34

Reference yield:

1-(benzyloxy)-4-(1′,2′,4′-triazol-1′-yl)-2-(1H)-pyrimidinone (219992-65-1) → Nα-tert-butoxycarbonyl-Nε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl Nε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanyl-Nε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine methyl ester (522644-19-5)

Guidance literature:

Multi-step reaction with 5 steps

1: 83 percent / CH₂Cl₂ / 144 h / 40 °C

2: 98 percent / aq. NaOH / methanol / 3 h / 20 °C

3: 87 percent / N-methylmorpholine; HOBt*H₂O; WSC*HCl / CH₂Cl₂ / 50 h / 0 - 20 °C

4: 85 percent / aq. NaOH / methanol / 20 °C

5: 82 percent / N-methylmorpholine; HOBt*H₂O; WSC*HCl / dimethylformamide; CH₂Cl₂ / 73 h / 0 - 20 °C

With 4-methyl-morpholine; sodium hydroxide; WSC*HCl; benzotriazol-1-ol; In methanol; dichloromethane; N,N-dimethyl-formamide;

DOI:10.3987/COM-02-S(M)34

upstream raw materials:

N^α-tert-butoxycarbonyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysyl-β-alanine

N-α-(tert-butoxycarbonyl)-L-lysine methyl ester

1-(benzyloxy)-4-(1′,2′,4′-triazol-1′-yl)-2-(1H)-pyrimidinone

N^α-tert-butoxycarbonyl-N^ε-(1-benzyloxy-1,2-dihydro-2-oxopyrimidin-4-yl)-L-lysine

Downstream raw materials:

C₆₅H₈₅N₁₅O₁₅

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