N2-acetyl-N-[(1S)-1-(ethoxycarbonyl)-2-methylpropyl]-2-methyl-D-α-asparaginyl-4-(dibenzylamino)-D-isovalyl-L-valine ethyl ester

Base Information

• Chemical Name: N2-acetyl-N-[(1S)-1-(ethoxycarbonyl)-2-methylpropyl]-2-methyl-D-α-asparaginyl-4-(dibenzylamino)-D-isovalyl-L-valine ethyl ester
• CAS No.: 1268691-55-9
• Molecular Formula: C₄₀H₅₉N₅O₈
• Molecular Weight: 737.937
• Mol file: 1268691-55-9.mol

Synonyms:

Chemical Property of N2-acetyl-N-[(1S)-1-(ethoxycarbonyl)-2-methylpropyl]-2-methyl-D-α-asparaginyl-4-(dibenzylamino)-D-isovalyl-L-valine ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N2-acetyl-N-[(1S)-1-(ethoxycarbonyl)-2-methylpropyl]-2-methyl-D-α-asparaginyl-4-(dibenzylamino)-D-isovalyl-L-valine ethyl ester

There total 5 articles about N2-acetyl-N-[(1S)-1-(ethoxycarbonyl)-2-methylpropyl]-2-methyl-D-α-asparaginyl-4-(dibenzylamino)-D-isovalyl-L-valine ethyl 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:

(2R,5S)-(6-ethoxy-5-isopropyl-2-methyl-3-oxo-2,3,4,5-tetrahydro-pyrazin-2-yl)-acetic acid (908298-93-1) → N2-acetyl-N-[(1S)-1-(ethoxycarbonyl)-2-methylpropyl]-2-methyl-D-α-asparaginyl-4-(dibenzylamino)-D-isovalyl-L-valine ethyl ester (1268691-55-9)

Guidance literature:

Multi-step reaction with 3 steps

1: triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride / tetrahydrofuran / 12 h / 20 °C

2: hydrogenchloride / ethanol; water / 12 h / 20 °C

3: triethylamine / dichloromethane

With hydrogenchloride; triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In tetrahydrofuran; ethanol; dichloromethane; water;

DOI:10.1002/hlca.201000202

Reference yield:

(3R,6S)-3-[2-(dibenzylamino)ethyl]-5-ethoxy-3,6-dihydro-6-isopropyl-3-methylpyrazin-2(1H)-one (1268691-39-9) → N2-acetyl-N-[(1S)-1-(ethoxycarbonyl)-2-methylpropyl]-2-methyl-D-α-asparaginyl-4-(dibenzylamino)-D-isovalyl-L-valine ethyl ester (1268691-55-9)

Guidance literature:

Multi-step reaction with 4 steps

1: hydrogenchloride / ethanol; water / 12 h / 20 °C

2: triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride / tetrahydrofuran / 12 h / 20 °C

3: hydrogenchloride / ethanol; water / 12 h / 20 °C

4: triethylamine / dichloromethane

With hydrogenchloride; triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In tetrahydrofuran; ethanol; dichloromethane; water;

DOI:10.1002/hlca.201000202

Reference yield:

4-(dibenzylamino)-N-{2-[(2R,5S)-6-ethoxy-2,3,4,5-tetrahydro-2-methyl-5-isopropyl-3-oxopyrazin-2-yl]acetyl}-D-isovalyl-L-valine ethyl ester (1268691-47-9) → N2-acetyl-N-[(1S)-1-(ethoxycarbonyl)-2-methylpropyl]-2-methyl-D-α-asparaginyl-4-(dibenzylamino)-D-isovalyl-L-valine ethyl ester (1268691-55-9)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogenchloride / ethanol; water / 12 h / 20 °C

2: triethylamine / dichloromethane

With hydrogenchloride; triethylamine; In ethanol; dichloromethane; water;

DOI:10.1002/hlca.201000202

upstream raw materials:

(2R,5S)-(6-ethoxy-5-isopropyl-2-methyl-3-oxo-2,3,4,5-tetrahydro-pyrazin-2-yl)-acetic acid

(3R,6S)-1-benzyl-3-methyl-3-(2-dibenzylaminoethyl)-5-ethoxy-1,6-dihydro-6-isopropylpyrazin-2-(3H)-one

4-(dibenzylamino)-N-{2-[(2R,5S)-6-ethoxy-2,3,4,5-tetrahydro-2-methyl-5-isopropyl-3-oxopyrazin-2-yl]acetyl}-D-isovalyl-L-valine ethyl ester

(3R,6S)-3-[2-(dibenzylamino)ethyl]-5-ethoxy-3,6-dihydro-6-isopropyl-3-methylpyrazin-2(1H)-one