Benzenesulfonamide, 4-(2-(2-(4-chlorophenyl)-1H-indol-3-yl)hydrazino)-N-(4,6-dimethyl-2-pyrimidinyl)-

Base Information

Chemical Name:Benzenesulfonamide, 4-(2-(2-(4-chlorophenyl)-1H-indol-3-yl)hydrazino)-N-(4,6-dimethyl-2-pyrimidinyl)-
CAS No.:88152-04-9
Molecular Formula:C26H23 Cl N6 O2 S
Molecular Weight:519.027
Hs Code.:
DSSTox Substance ID:DTXSID40236861
Wikidata:Q83118951

Synonyms:88152-04-9;Benzenesulfonamide, 4-(2-(2-(4-chlorophenyl)-1H-indol-3-yl)hydrazino)-N-(4,6-dimethyl-2-pyrimidinyl)-;4-(2-(2-(4-Chlorophenyl)-1H-indol-3-yl)hydrazinyl)-N-(4,6-dimethylpyrimidin-2-yl)benzenesulfonamide;BRN 4615217;DTXSID40236861

Suppliers and Price of Benzenesulfonamide, 4-(2-(2-(4-chlorophenyl)-1H-indol-3-yl)hydrazino)-N-(4,6-dimethyl-2-pyrimidinyl)-

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
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Total 1 raw suppliers

Chemical Property of Benzenesulfonamide, 4-(2-(2-(4-chlorophenyl)-1H-indol-3-yl)hydrazino)-N-(4,6-dimethyl-2-pyrimidinyl)-

Chemical Property:

XLogP3:6.1
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:518.1291729
Heavy Atom Count:36
Complexity:802

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=NC(=N1)NS(=O)(=O)C2=CC=C(C=C2)NNC3=C(NC4=CC=CC=C43)C5=CC=C(C=C5)Cl)C

Technology Process of Benzenesulfonamide, 4-(2-(2-(4-chlorophenyl)-1H-indol-3-yl)hydrazino)-N-(4,6-dimethyl-2-pyrimidinyl)-

There total 3 articles about Benzenesulfonamide, 4-(2-(2-(4-chlorophenyl)-1H-indol-3-yl)hydrazino)-N-(4,6-dimethyl-2-pyrimidinyl)- 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%

: 88151-95-5
4-[2-(4-Chloro-phenyl)-1H-indol-3-ylazo]-N-(4,6-dimethyl-pyrimidin-2-yl)-benzenesulfonamide

: 88152-04-9
4-{N'-[2-(4-Chloro-phenyl)-1H-indol-3-yl]-hydrazino}-N-(4,6-dimethyl-pyrimidin-2-yl)-benzenesulfonamide

Guidance literature:: With hydrazine hydrate; nickel; In ethanol; for 4h; Heating;

Reference yield:

: 1211-35-4
2-(4-chlorophenyl)-1H-indole

: 88152-04-9
4-{N'-[2-(4-Chloro-phenyl)-1H-indol-3-yl]-hydrazino}-N-(4,6-dimethyl-pyrimidin-2-yl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / pyridine / 1) cooled in ice, 1 h 2) room temperature, 1 h 3) reflux, 4 h

2: 60 percent / Hydrazine hydrate / Raney-Ni / ethanol / 4 h / Heating

With hydrazine hydrate; nickel; In pyridine; ethanol;

Reference yield:

: 131430-30-3
C₁₂H₁₂ClN₅O₂S

: 88152-04-9
4-{N'-[2-(4-Chloro-phenyl)-1H-indol-3-yl]-hydrazino}-N-(4,6-dimethyl-pyrimidin-2-yl)-benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / pyridine / 1) cooled in ice, 1 h 2) room temperature, 1 h 3) reflux, 4 h

2: 60 percent / Hydrazine hydrate / Raney-Ni / ethanol / 4 h / Heating

With hydrazine hydrate; nickel; In pyridine; ethanol;