(5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanone

Base Information

• Chemical Name: (5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanone
• CAS No.: 244241-90-5
• Molecular Formula: C₃₂H₂₉ClN₂O₅
• Molecular Weight: 557.046
• Mol file: 244241-90-5.mol

Synonyms:(5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanone

Chemical Property of (5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanone

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanone

There total 2 articles about (5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanone 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: 53.0%

5,6,7-trimethoxy-1H-indole-2-carboxylic acid (128781-07-7) + 5-benzyloxy-1-chloromethyl-2,3-dihydro-1H-benzo[e]indole; hydrochloride → (5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanone (244241-90-5)

Guidance literature:

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;

DOI:10.1021/jo990452y

Reference yield:

5-(benzyloxy)-3-(tert-butyloxycarbonyl)-1-(chloromethyl)-1,2-dihydro-3H-benzindole (128300-12-9) → (5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanone (244241-90-5)

Guidance literature:

Multi-step reaction with 2 steps

1: HCl / ethyl acetate

2: 53 percent / EDCI

With hydrogenchloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In ethyl acetate;

DOI:10.1021/jo990452y

Reference yield: 88.0%

(5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanone (244241-90-5) → (5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanethione (244241-91-6)

Guidance literature:

With Lawessons reagent; In benzene; at 80 ℃; for 1.5h;

DOI:10.1021/jo990452y

upstream raw materials:

5,6,7-trimethoxy-1H-indole-2-carboxylic acid

5-(benzyloxy)-3-(tert-butyloxycarbonyl)-1-(chloromethyl)-1,2-dihydro-3H-benzindole

Downstream raw materials:

(5-benzyloxy-1-chloromethyl-1,2-dihydro-benzo[e]indol-3-yl)-(5,6,7-trimethoxy-1H-indol-2-yl)-methanethione