methyl (S)-5-(benzyloxy)-1-(chloromethyl)-3-(5-acetylindole-2-carbonyl)-1,2-dihydropyrrolo[3,2-e]indole-2-carboxylate

Base Information

• Chemical Name: methyl (S)-5-(benzyloxy)-1-(chloromethyl)-3-(5-acetylindole-2-carbonyl)-1,2-dihydropyrrolo[3,2-e]indole-2-carboxylate
• CAS No.: 1228694-02-7
• Molecular Formula: C₃₁H₂₆ClN₃O₅
• Molecular Weight: 556.018
• Mol file: 1228694-02-7.mol

Synonyms:methyl (S)-5-(benzyloxy)-1-(chloromethyl)-3-(5-acetylindole-2-carbonyl)-1,2-dihydropyrrolo[3,2-e]indole-2-carboxylate

Chemical Property of methyl (S)-5-(benzyloxy)-1-(chloromethyl)-3-(5-acetylindole-2-carbonyl)-1,2-dihydropyrrolo[3,2-e]indole-2-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl (S)-5-(benzyloxy)-1-(chloromethyl)-3-(5-acetylindole-2-carbonyl)-1,2-dihydropyrrolo[3,2-e]indole-2-carboxylate

There total 5 articles about methyl (S)-5-(benzyloxy)-1-(chloromethyl)-3-(5-acetylindole-2-carbonyl)-1,2-dihydropyrrolo[3,2-e]indole-2-carboxylate 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: 55.0%

5-acetyl-1H-indole-2-carboxylic acid (31380-57-1) + (S)-8-Chloromethyl-4-hydroxy-3,6,7,8-tetrahydro-pyrrolo[3,2-e]indole-2-carboxylic acid methyl ester; hydrochloride → methyl (S)-5-(benzyloxy)-1-(chloromethyl)-3-(5-acetylindole-2-carbonyl)-1,2-dihydropyrrolo[3,2-e]indole-2-carboxylate (1228694-02-7)

Guidance literature:

With sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 25 ℃; for 0.5h;

DOI:10.1016/j.bmcl.2010.03.078

Reference yield:

3,6-di-tert-butyl 7-methyl (S)-1-(chloromethyl)-5-hydroxy-1,2-dihydropyrrolo[3,2-e]indole-3,6,7-tricarboxylate (919535-18-5) → methyl (S)-5-(benzyloxy)-1-(chloromethyl)-3-(5-acetylindole-2-carbonyl)-1,2-dihydropyrrolo[3,2-e]indole-2-carboxylate (1228694-02-7)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogenchloride / ethyl acetate / 25 °C

2: sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethyl acetate; N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2010.03.078

Reference yield:

4-acetyl-2-iodoaniline (97776-06-2) → methyl (S)-5-(benzyloxy)-1-(chloromethyl)-3-(5-acetylindole-2-carbonyl)-1,2-dihydropyrrolo[3,2-e]indole-2-carboxylate (1228694-02-7)

Guidance literature:

Multi-step reaction with 2 steps

1: 1,4-diaza-bicyclo[2.2.2]octane; palladium diacetate / N,N-dimethyl-formamide / 4 h / 105 °C / Inert atmosphere

2: sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 20 °C

With 1,4-diaza-bicyclo[2.2.2]octane; palladium diacetate; sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide;

DOI:10.1016/j.bmcl.2010.03.078

upstream raw materials:

5-acetyl-1H-indole-2-carboxylic acid

3,6-di-tert-butyl 7-methyl (S)-1-(chloromethyl)-5-hydroxy-1,2-dihydropyrrolo[3,2-e]indole-3,6,7-tricarboxylate

p-aminobenzophenone

4-acetyl-2-iodoaniline