4-amino-N-(2-cyclopentylbenzotriazol-5-yl)benzenesulfonamide

Base Information

Chemical Name:4-amino-N-(2-cyclopentylbenzotriazol-5-yl)benzenesulfonamide
CAS No.:130787-24-5
Molecular Formula:C₁₇H₁₉N₅O₂S
Molecular Weight:357.436
Hs Code.:
DSSTox Substance ID:DTXSID50872234
Nikkaji Number:J1.564.282C

Synonyms:130787-24-5;DTXSID50872234;4-Amino-N-(2-cyclopentyl-2H-benzotriazol-5-yl)benzene-1-sulfonamide

Suppliers and Price of 4-amino-N-(2-cyclopentylbenzotriazol-5-yl)benzenesulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 4-amino-N-(2-cyclopentylbenzotriazol-5-yl)benzenesulfonamide

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:357.12594604
Heavy Atom Count:25
Complexity:552

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC(C1)N2N=C3C=CC(=CC3=N2)NS(=O)(=O)C4=CC=C(C=C4)N

Technology Process of 4-amino-N-(2-cyclopentylbenzotriazol-5-yl)benzenesulfonamide

There total 6 articles about 4-amino-N-(2-cyclopentylbenzotriazol-5-yl)benzenesulfonamide 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: 90.0%

: 130787-27-8
2-cyclopentyl-5-(p-acetamidobenzensulfonamido)benzotriazole

: 130787-24-5
2-cyclopentyl-5-(p-aminobenzensulfonamido)benzotriazole

Guidance literature:: With sodium hydroxide; for 1h; Heating;
DOI:10.1016/0223-5234(90)90118-M

Reference yield:

: 137-43-9
Cyclopentyl bromide

: 130787-24-5
2-cyclopentyl-5-(p-aminobenzensulfonamido)benzotriazole

Guidance literature:: Multi-step reaction with 4 steps

1: 38 percent / C₂H₅ONa / 24 h / Heating

2: 100 percent / H₂ / 10percent Pd/C / methanol / Ambient temperature

3: 72 percent / pyridine / 1.) a) RT, 20 h, b) 60 deg C, 8 h

4: 90 percent / 2 N NaOH / 1 h / Heating

With pyridine; sodium hydroxide; hydrogen; sodium ethanolate; palladium on activated charcoal; In methanol;
DOI:10.1016/0223-5234(90)90118-M

Reference yield:

: 2338-12-7
5-nitrobenzotriazole

: 130787-24-5
2-cyclopentyl-5-(p-aminobenzensulfonamido)benzotriazole

Guidance literature:: Multi-step reaction with 4 steps

1: 38 percent / C₂H₅ONa / 24 h / Heating

2: 100 percent / H₂ / 10percent Pd/C / methanol / Ambient temperature

3: 72 percent / pyridine / 1.) a) RT, 20 h, b) 60 deg C, 8 h

4: 90 percent / 2 N NaOH / 1 h / Heating

With pyridine; sodium hydroxide; hydrogen; sodium ethanolate; palladium on activated charcoal; In methanol;
DOI:10.1016/0223-5234(90)90118-M