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Imidazo[1,2-c]quinazoline, 2,3-dihydro-3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-5-(methylthio) -, (3S)-

Base Information Edit
  • Chemical Name:Imidazo[1,2-c]quinazoline, 2,3-dihydro-3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-5-(methylthio) -, (3S)-
  • CAS No.:180959-12-0
  • Molecular Formula:C23H27N5OS
  • Molecular Weight:421.566
  • Hs Code.:
  • Mol file:180959-12-0.mol
Imidazo[1,2-c]quinazoline,
2,3-dihydro-3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-5-(methylthio)
-, (3S)-

Synonyms:

Suppliers and Price of Imidazo[1,2-c]quinazoline, 2,3-dihydro-3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-5-(methylthio) -, (3S)-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Imidazo[1,2-c]quinazoline, 2,3-dihydro-3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-5-(methylthio) -, (3S)- Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Imidazo[1,2-c]quinazoline, 2,3-dihydro-3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-5-(methylthio) -, (3S)-

There total 9 articles about Imidazo[1,2-c]quinazoline, 2,3-dihydro-3-[[4-(2-methoxyphenyl)-1-piperazinyl]methyl]-5-(methylthio) -, (3S)- 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 potassium carbonate; methanesulfonyl chloride; triethylamine; In dichloromethane; at 2 - 25 ℃; for 25h; Yields of byproduct given;
DOI:10.1016/0957-4166(96)00198-X
Guidance literature:
Multi-step reaction with 4 steps
1: 73 percent / tetrahydrofuran / 72 h / Heating
2: 86 percent / NH2NH2*H2O / ethanol / 12 h / 25 °C
3: 33 percent / acetonitrile / 96 h / Heating
4: 75 percent / MsCl, Et3N, K2CO3 / CH2Cl2 / 25 h / 2 - 25 °C
With potassium carbonate; hydrazine hydrate; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; acetonitrile;
DOI:10.1016/0957-4166(96)00198-X
Guidance literature:
Multi-step reaction with 2 steps
1: 33 percent / acetonitrile / 96 h / Heating
2: 75 percent / MsCl, Et3N, K2CO3 / CH2Cl2 / 25 h / 2 - 25 °C
With potassium carbonate; methanesulfonyl chloride; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1016/0957-4166(96)00198-X
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