9-benzenesulfonyl-7-methoxy-2-(2-nitrobenzenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-6-ol

Base Information

Chemical Name:9-benzenesulfonyl-7-methoxy-2-(2-nitrobenzenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-6-ol
CAS No.:267666-35-3
Molecular Formula:C₂₄H₂₁N₃O₈S₂
Molecular Weight:543.578
Hs Code.:

Synonyms:9-benzenesulfonyl-7-methoxy-2-(2-nitrobenzenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-6-ol

Suppliers and Price of 9-benzenesulfonyl-7-methoxy-2-(2-nitrobenzenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-6-ol

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 9-benzenesulfonyl-7-methoxy-2-(2-nitrobenzenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-6-ol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 9-benzenesulfonyl-7-methoxy-2-(2-nitrobenzenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-6-ol

There total 3 articles about 9-benzenesulfonyl-7-methoxy-2-(2-nitrobenzenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-6-ol 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: 80.0%

: N-(3-methoxy-4-oxo-cyclohexa-2,5-dienylidene)-benzenesulfonamide

: 1026716-28-8
3,3-dimethoxy-1-(2-nitro-benzenesulfonyl)-piperidine

: 267666-35-3
9-benzenesulfonyl-7-methoxy-2-(2-nitrobenzenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-6-ol

Guidance literature:: 3,3-dimethoxy-1-(2-nitro-benzenesulfonyl)-piperidine; With aluminium trichloride; triethylamine; In diethyl ether; at 20 ℃;

N-(3-methoxy-4-oxo-cyclohexa-2,5-dienylidene)-benzenesulfonamide; With titanium(IV) isopropylate; titanium tetrachloride; In dichloromethane; at -78 - 20 ℃; for 10h;

With ammonium chloride; In dichloromethane; for 0.5h; Further stages.;
DOI:10.1021/jo9916176

Reference yield:

: 1694-92-4
2-Nitrobenzenesulfonyl chloride

: 267666-35-3
9-benzenesulfonyl-7-methoxy-2-(2-nitrobenzenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-6-ol

Guidance literature:: Multi-step reaction with 3 steps

1.1: 88 percent / K₂CO₃ / H₂O; CHCl₃ / 10 h / 20 °C

2.1: p-TsOH*H₂O / 10 h

3.1: AlCl₃; Et₃N / diethyl ether / 20 °C

3.2: TiCl₄; Ti(OiPr)4 / CH₂Cl₂ / 10 h / -78 - 20 °C

3.3: 80 percent / aq. NH₄Cl / CH₂Cl₂ / 0.5 h

With aluminium trichloride; potassium carbonate; toluene-4-sulfonic acid; triethylamine; In diethyl ether; chloroform; water; 1.1: Substitution / 2.1: Addition / 3.1: Elimination / 3.2: cyclocondensation / 3.3: Elimination;
DOI:10.1021/jo9916176

Reference yield:

: 267666-12-6
1-(2-nitro-benzenesulfonyl)-piperidin-3-one

: 267666-35-3
9-benzenesulfonyl-7-methoxy-2-(2-nitrobenzenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-6-ol

Guidance literature:: Multi-step reaction with 2 steps

1.1: p-TsOH*H₂O / 10 h

2.1: AlCl₃; Et₃N / diethyl ether / 20 °C

2.2: TiCl₄; Ti(OiPr)4 / CH₂Cl₂ / 10 h / -78 - 20 °C

2.3: 80 percent / aq. NH₄Cl / CH₂Cl₂ / 0.5 h

With aluminium trichloride; toluene-4-sulfonic acid; triethylamine; In diethyl ether; 1.1: Addition / 2.1: Elimination / 2.2: cyclocondensation / 2.3: Elimination;
DOI:10.1021/jo9916176