[3-(Benzyloxycarbonyl-ethyl-amino)-propyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamic acid benzyl ester

Base Information

• Chemical Name: [3-(Benzyloxycarbonyl-ethyl-amino)-propyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamic acid benzyl ester
• CAS No.: 180523-60-8
• Molecular Formula: C₃₂H₃₅N₃O₆
• Molecular Weight: 557.646
• Mol file: 180523-60-8.mol

Synonyms:[3-(Benzyloxycarbonyl-ethyl-amino)-propyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamic acid benzyl ester

Chemical Property of [3-(Benzyloxycarbonyl-ethyl-amino)-propyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [3-(Benzyloxycarbonyl-ethyl-amino)-propyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamic acid benzyl ester

There total 4 articles about [3-(Benzyloxycarbonyl-ethyl-amino)-propyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamic acid benzyl 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: 60.0%

benzyl chloroformate (501-53-1,94274-21-2) + 2-[3-(3-Ethylamino-propylamino)-propyl]-isoindole-1,3-dione; hydrobromide → [3-(Benzyloxycarbonyl-ethyl-amino)-propyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamic acid benzyl ester (180523-60-8)

Guidance literature:

With sodium hydrogencarbonate; sodium chloride; In chloroform; for 3h; Heating;

DOI:10.1016/0968-0896(96)00072-7

Reference yield:

1-phthalimido-4-(N-benzyl)-7-<<(2-mesitylene)sulfonyl>amino>-4-azaheptane (151915-06-9) → [3-(Benzyloxycarbonyl-ethyl-amino)-propyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamic acid benzyl ester (180523-60-8)

Guidance literature:

Multi-step reaction with 4 steps

1: 1.) NaH / 1.) DMF, 0 deg C, 30 min, 2.) DMF, a) 0 deg C, 30 min, b) RT, 45 min

2: 60 percent / H₂ / methanol; ethanol / 48 h / 2585.7 Torr / Ambient temperature

3: phenol, 30percent HBr/HOAc / ethyl acetate / 18 h / Heating

4: 60 percent / aq. NaHCO₃, NaCl / CHCl₃ / 3 h / Heating

With hydrogen bromide; hydrogen; sodium hydride; sodium hydrogencarbonate; acetic acid; sodium chloride; phenol; In methanol; ethanol; chloroform; ethyl acetate;

DOI:10.1016/0968-0896(96)00072-7

Reference yield:

N-{3-[3-(1,3-Dioxo-1,3-dihydro-isoindol-2-yl)-propylamino]-propyl}-N-ethyl-2,4,6-trimethyl-benzenesulfonamide → [3-(Benzyloxycarbonyl-ethyl-amino)-propyl]-[3-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-propyl]-carbamic acid benzyl ester (180523-60-8)

Guidance literature:

Multi-step reaction with 2 steps

1: phenol, 30percent HBr/HOAc / ethyl acetate / 18 h / Heating

2: 60 percent / aq. NaHCO₃, NaCl / CHCl₃ / 3 h / Heating

With hydrogen bromide; sodium hydrogencarbonate; acetic acid; sodium chloride; phenol; In chloroform; ethyl acetate;

DOI:10.1016/0968-0896(96)00072-7

upstream raw materials:

benzyl chloroformate

1-phthalimido-4-(N-benzyl)-7-<<(2-mesitylene)sulfonyl>amino>-4-azaheptane

Downstream raw materials:

1-{N-[benzyloxy(methyl)phosphinyl]amino}-4-N-(carbobenzyloxy)-7-[N-ethyl-N-(carbobenzyloxy)amino]-4-azaheptane

{3-[(3-Amino-propyl)-benzyloxycarbonyl-amino]-propyl}-ethyl-carbamic acid benzyl ester