1-(benzyloxycarbonyl)-3-[2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)-benzoyl]guanidine

Base Information

Chemical Name:1-(benzyloxycarbonyl)-3-[2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)-benzoyl]guanidine
CAS No.:294204-23-2
Molecular Formula:C₂₂H₂₂N₄O₅S
Molecular Weight:454.506
Hs Code.:

Synonyms:1-(benzyloxycarbonyl)-3-[2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)-benzoyl]guanidine

Suppliers and Price of 1-(benzyloxycarbonyl)-3-[2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)-benzoyl]guanidine

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 0 raw suppliers

Chemical Property of 1-(benzyloxycarbonyl)-3-[2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)-benzoyl]guanidine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-(benzyloxycarbonyl)-3-[2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)-benzoyl]guanidine

There total 4 articles about 1-(benzyloxycarbonyl)-3-[2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)-benzoyl]guanidine 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: 87.0%

: 16706-54-0
N-Cbz-guanidine

: 294204-22-1
2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)benzoic acid

: 294204-23-2
1-(benzyloxycarbonyl)-3-[2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)-benzoyl]guanidine

Guidance literature:: With 2-chloro-1-methyl-pyridinium iodide; N-ethyl-N,N-diisopropylamine; In various solvent(s); at 20 ℃; for 2h;
DOI:10.1002/1099-0690(200006)2000:12<2253::AID-EJOC2253>3.0.CO;2-Q

Reference yield:

: 452-63-1
2-Bromo-5-fluorotoluene

: 294204-23-2
1-(benzyloxycarbonyl)-3-[2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)-benzoyl]guanidine

Guidance literature:: Multi-step reaction with 4 steps

1.1: SOCl₂ / 1 h / Heating

1.2: 65 percent / trifluoromethanesulfonic acid / 3 h / 125 °C

2.1: 92 percent / KOAc; Pd(OAc)2; dppf / dimethylsulfoxide; H₂O / 89 h / 82 °C / 19001.3 - 22801.5 Torr

3.1: 77 percent / NaH / dimethylsulfoxide / 3 h / 20 °C

4.1: 87 percent / 2-chloro-1-methylpyridinium iodide; (iPr)2NEt / various solvent(s) / 2 h / 20 °C

With 1,1'-bis-(diphenylphosphino)ferrocene; palladium diacetate; thionyl chloride; 2-chloro-1-methyl-pyridinium iodide; potassium acetate; sodium hydride; N-ethyl-N,N-diisopropylamine; In water; dimethyl sulfoxide; 1.1: Chlorination / 1.2: Substitution / 2.1: Carbonylation / 3.1: Alkylation / 4.1: Acylation;
DOI:10.1002/1099-0690(200006)2000:12<2253::AID-EJOC2253>3.0.CO;2-Q

Reference yield:

: 190367-38-5
4-fluoro-2-methyl-5-(methylsulfonyl)benzoic acid

: 294204-23-2
1-(benzyloxycarbonyl)-3-[2-methyl-5-methylsulfonyl-4-(pyrrol-1-yl)-benzoyl]guanidine

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / NaH / dimethylsulfoxide / 3 h / 20 °C

2: 87 percent / 2-chloro-1-methylpyridinium iodide; (iPr)2NEt / various solvent(s) / 2 h / 20 °C

With 2-chloro-1-methyl-pyridinium iodide; sodium hydride; N-ethyl-N,N-diisopropylamine; In dimethyl sulfoxide; 1: Alkylation / 2: Acylation;
DOI:10.1002/1099-0690(200006)2000:12<2253::AID-EJOC2253>3.0.CO;2-Q