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6-Chloro-5-methyl-1-((2-(2-methylpyrid-3-yloxy)pyrid-5-yl)carbamoyl)indoline

Base Information
  • Chemical Name:6-Chloro-5-methyl-1-((2-(2-methylpyrid-3-yloxy)pyrid-5-yl)carbamoyl)indoline
  • CAS No.:181632-25-7
  • Molecular Formula:C21H19ClN4O2
  • Molecular Weight:394.86
  • Hs Code.:
  • UNII:9FEE9A2U4Z
  • DSSTox Substance ID:DTXSID401017151
  • Nikkaji Number:J853.940E
  • Wikipedia:SB-242084
  • Wikidata:Q7388908
  • Pharos Ligand ID:MZGNDB1S6VJ4
  • ChEMBL ID:CHEMBL14563
  • Mol file:181632-25-7.mol
6-Chloro-5-methyl-1-((2-(2-methylpyrid-3-yloxy)pyrid-5-yl)carbamoyl)indoline

Synonyms:6-chloro-5-methyl-1-((2-(2-methylpyrid-3-yloxy)pyrid-5-yl)carbamoyl)indoline;SB 242084;SB-242084;SB242084

Suppliers and Price of 6-Chloro-5-methyl-1-((2-(2-methylpyrid-3-yloxy)pyrid-5-yl)carbamoyl)indoline
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
  • TRC
  • SB242084
  • 100mg
  • $ 1455.00
  • Tocris
  • SB242084 ≥99%(HPLC)
  • 50
  • $ 942.00
  • Tocris
  • SB242084 ≥99%(HPLC)
  • 10
  • $ 225.00
  • Sigma-Aldrich
  • SB 242084 dihydrochloride hydrate ≥98% (HPLC), powder
  • 25mg
  • $ 3090.00
  • Sigma-Aldrich
  • SB 242084 Hydrochloride - CAS 181632-25-7 - Calbiochem
  • 10 mg
  • $ 169.00
  • Sigma-Aldrich
  • SB 242084 Hydrochloride - CAS 181632-25-7 - Calbiochem
  • 5064170001
  • $ 163.00
  • Sigma-Aldrich
  • SB 242084 dihydrochloride hydrate ≥98% (HPLC), powder
  • 5mg
  • $ 896.00
  • Medical Isotopes, Inc.
  • SB242084
  • 100 mg
  • $ 2200.00
  • Matrix Scientific
  • 6-Chloro-5-methyl-N-(6-((2-methylpyridin-3-yl)oxy)pyridin-3-yl)indoline-1-carboxamide dihydrochloride 95+%
  • 1g
  • $ 3200.00
  • Matrix Scientific
  • 6-Chloro-5-methyl-N-(6-((2-methylpyridin-3-yl)oxy)pyridin-3-yl)indoline-1-carboxamide dihydrochloride 95+%
  • 250mg
  • $ 1352.00
Total 39 raw suppliers
Chemical Property of 6-Chloro-5-methyl-1-((2-(2-methylpyrid-3-yloxy)pyrid-5-yl)carbamoyl)indoline
Chemical Property:
  • Melting Point:181-183℃ 
  • Boiling Point:620.1±55.0 °C(Predicted) 
  • PKA:12.47±0.20(Predicted) 
  • PSA:67.35000 
  • Density:1.362±0.06 g/cm3(Predicted) 
  • LogP:6.87570 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO: soluble15mg/mL, clear 
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:394.1196536
  • Heavy Atom Count:28
  • Complexity:551
Purity/Quality:

99%, *data from raw suppliers

SB242084 *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:CC1=CC2=C(C=C1Cl)N(CC2)C(=O)NC3=CN=C(C=C3)OC4=C(N=CC=C4)C
  • Uses SB 242084 is a 5-HT2C receptor antagonist that displays 158- and 100-fold selectivity over 5-HT2A and 5-HT2B receptors respectively. SB 242084 displays selectivity over a range of other 5-HT, dopamine and adrenergic receptors.SB 242084 os a brain penetrant; exerts anxiolytic-like activity. SB 242084 is a 5-HT2C receptor antagonist that displays 158- and 100-fold selectivity over 5-HT2A and 5-HT2B receptors respectively. SB 242084 displays selectivity over a range of other 5-HT, dopamine and adrenergic receptors.SB 242084 os a brain penetrant; exerts anxiolytic-like activity.
Technology Process of 6-Chloro-5-methyl-1-((2-(2-methylpyrid-3-yloxy)pyrid-5-yl)carbamoyl)indoline

There total 10 articles about 6-Chloro-5-methyl-1-((2-(2-methylpyrid-3-yloxy)pyrid-5-yl)carbamoyl)indoline 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:
Guidance literature:
With triethylamine; In N,N-dimethyl-formamide; at 100 ℃; for 1h;
DOI:10.1021/jm970424c
Guidance literature:
Multi-step reaction with 4 steps
1.1: NaH / dimethylformamide / 3.25 h / 0 - 20 °C
1.2: 95 percent / dimethylformamide / 18 h / 20 °C
2.1: 86 percent / SnCl2; conc. HCl / ethanol / 1 h / 50 °C
3.1: 56 percent / Et3N / CH2Cl2 / 1 h / -20 °C
4.1: 71 percent / Et3N / dimethylformamide / 1 h / 95 - 105 °C
With hydrogenchloride; sodium hydride; triethylamine; tin(ll) chloride; In ethanol; dichloromethane; N,N-dimethyl-formamide; 1.1: Metallation / 1.2: Substitution / 2.1: Reduction / 3.1: Condensation / 4.1: Substitution;
DOI:10.1021/jm990388c
Guidance literature:
Multi-step reaction with 3 steps
1: 86 percent / SnCl2; conc. HCl / ethanol / 1 h / 50 °C
2: 56 percent / Et3N / CH2Cl2 / 1 h / -20 °C
3: 71 percent / Et3N / dimethylformamide / 1 h / 95 - 105 °C
With hydrogenchloride; triethylamine; tin(ll) chloride; In ethanol; dichloromethane; N,N-dimethyl-formamide; 1: Reduction / 2: Condensation / 3: Substitution;
DOI:10.1021/jm990388c
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