1H-Pyrazolo[3,4-b]pyridine-6-carboxamide, 1-phenyl-

Base Information

Chemical Name:1H-Pyrazolo[3,4-b]pyridine-6-carboxamide, 1-phenyl-
CAS No.:116855-17-5
Molecular Formula:C₁₃H₁₀N₄O
Molecular Weight:238.249
Hs Code.:
DSSTox Substance ID:DTXSID601223166

Synonyms:116855-17-5;1H-Pyrazolo[3,4-b]pyridine-6-carboxamide, 1-phenyl-;SCHEMBL18705466;DTXSID601223166

Suppliers and Price of 1H-Pyrazolo[3,4-b]pyridine-6-carboxamide, 1-phenyl-

Supply Marketing:

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

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Chemical Property of 1H-Pyrazolo[3,4-b]pyridine-6-carboxamide, 1-phenyl-

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:238.08546096
Heavy Atom Count:18
Complexity:316

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)N2C3=C(C=CC(=N3)C(=O)N)C=N2

Technology Process of 1H-Pyrazolo[3,4-b]pyridine-6-carboxamide, 1-phenyl-

There total 3 articles about 1H-Pyrazolo[3,4-b]pyridine-6-carboxamide, 1-phenyl- 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: 30.0%

: 77287-34-4,77287-35-5,60100-09-6
formamide

: 20208-81-5
1-phenyl-1H-pyrazolo[3,4-b]pyridine

: 116855-17-5
1-Phenyl-1H-pyrazolo[3,4-b]pyridine-6-carboxylic acid amide

Guidance literature:: With sulfuric acid; dihydrogen peroxide; iron(II) sulfate; at 10 - 15 ℃; for 0.5h;
DOI:10.1139/v88-074

Reference yield:

: 826-85-7
1-phenylpyrazol-5-amine

: 116855-17-5
1-Phenyl-1H-pyrazolo[3,4-b]pyridine-6-carboxylic acid amide

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / ZnCl₂ / aq. HCl; ethanol / 1 h / Heating

2: 30 percent / sulfuric acid, 30percent hydrogen peroxide, iron(II) sulfate heptahydrate / 0.5 h / 10 - 15 °C

With sulfuric acid; dihydrogen peroxide; iron(II) sulfate; zinc(II) chloride; In hydrogenchloride; ethanol;
DOI:10.1139/v88-074

Reference yield:

: 5334-43-0
5-Amino-4-cyano-1-phenylpyrazole

: 116855-17-5
1-Phenyl-1H-pyrazolo[3,4-b]pyridine-6-carboxylic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / 85percent phosphoric acid / 20 h / 170 - 180 °C

2: 97 percent / ZnCl₂ / aq. HCl; ethanol / 1 h / Heating

3: 30 percent / sulfuric acid, 30percent hydrogen peroxide, iron(II) sulfate heptahydrate / 0.5 h / 10 - 15 °C

With phosphoric acid; sulfuric acid; dihydrogen peroxide; iron(II) sulfate; zinc(II) chloride; In hydrogenchloride; ethanol;
DOI:10.1139/v88-074