[3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl]bis-(methylene)

Base Information

Chemical Name:[3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl]bis-(methylene)
CAS No.:1422377-25-0
Molecular Formula:C₃₁H₃₅ClN₄O₄
Molecular Weight:563.096
Hs Code.:

Synonyms:[3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl]bis-(methylene)

Suppliers and Price of [3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl]bis-(methylene)

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of [3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl]bis-(methylene)

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of [3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl]bis-(methylene)

There total 10 articles about [3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl]bis-(methylene) 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%

: 1422377-07-8
(3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl)dimethanol

: 1795-48-8
Isopropyl isocyanate

: 1422377-25-0
[3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl]bis-(methylene)

Guidance literature:: With triethylamine; at 20 ℃; Inert atmosphere;
DOI:10.1021/jm301788a

Reference yield:

: 1422376-98-4
dimethyl 3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino-[6,7-b]indole-1,2-dicarboxylate

: 1422377-25-0
[3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl]bis-(methylene)

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride / diethyl ether; dichloromethane / 0.5 h / -5 - 0 °C

2: triethylamine / 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; triethylamine; In diethyl ether; dichloromethane;
DOI:10.1021/jm301788a

Reference yield:

: 7524-52-9,26988-71-6,5619-09-0,14907-27-8,41222-70-2,67557-19-1,109492-62-8
(S)-tryptophan methyl ester hydrochloride

: 1422377-25-0
[3-(4-chlorophenyl)-6-methyl-6,11-dihydro-5H-indolizino[6,7-b]indole-1,2-diyl]bis-(methylene)

Guidance literature:: Multi-step reaction with 6 steps

1.1: water; methanol / 5 h / 20 °C

2.1: triethylamine / tetrahydrofuran / 9 h / Reflux

3.1: sodium hydride / mineral oil; tetrahydrofuran / 0.25 h / 0 - 5 °C

3.2: 9 h / 0 - 20 °C

3.3: pH 6

4.1: acetic anhydride / 60 - 75 °C

5.1: lithium aluminium tetrahydride / diethyl ether; dichloromethane / 0.5 h / -5 - 0 °C

6.1: triethylamine / 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; acetic anhydride; sodium hydride; triethylamine; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; mineral oil; 1.1: |Pictet-Spengler Synthesis;
DOI:10.1021/jm301788a