1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid

Base Information

Chemical Name:1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid
CAS No.:1260433-36-0
Molecular Formula:
Molecular Weight:0
Hs Code.:
DSSTox Substance ID:DTXSID50693249
Wikidata:Q82622290
Mol file:1260433-36-0.mol

Synonyms:1260433-36-0;1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid;(1H-Pyrrolo[2,3-b]pyridin-3-yl)boronic acid;1H-pyrrolo[2,3-b]pyridine-3-boronic acid;{1H-pyrrolo[2,3-b]pyridin-3-yl}boronic acid;DTXSID50693249;MFCD18414667;AKOS005214188;AB86020;CS-0055843;FT-0737277;(1H-Pyrrolo[2,3-b]pyridin-3-yl)boronicacid;EN300-150066

Suppliers and Price of 1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid

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 5 raw suppliers

Chemical Property of 1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid

Chemical Property:

Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:162.0600576
Heavy Atom Count:12
Complexity:168

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:B(C1=CNC2=C1C=CC=N2)(O)O

Technology Process of 1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid

There total 1 articles about 1H-pyrrolo[2,3-b]pyridin-3-ylboronic acid 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:

: 271-63-6
7-Azaindole

: 67-56-1
methanol

: 73183-34-3
bis(pinacol)diborane

: 1260433-36-0
{1H-pyrrolo[2,3-b]pyridin-3-yl}boronic acid

Guidance literature:: 7-Azaindole; bis(pinacol)diborane; With (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 3,4,7,8-Tetramethyl-o-phenanthrolin; In tetrahydrofuran; at 80 ℃; Sealed tube; Inert atmosphere;

methanol;

Reference yield:

: 1260433-36-0
{1H-pyrrolo[2,3-b]pyridin-3-yl}boronic acid

: 1365534-45-7
C₁₈H₁₅N₅O

Guidance literature:: Multi-step reaction with 3 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / 1,2-dimethoxyethane; N,N-dimethyl-formamide / 130 - 170 °C / Microwave irradiation

2: Oxone / water; ethyl acetate

3: 1,4-dioxane / Reflux

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; Oxone; potassium carbonate; In 1,4-dioxane; 1,2-dimethoxyethane; water; ethyl acetate; N,N-dimethyl-formamide; 1: Suzuki coupling;
DOI:10.1016/j.bmcl.2012.01.041

Reference yield:

: 1260433-36-0
{1H-pyrrolo[2,3-b]pyridin-3-yl}boronic acid

: 1365534-46-8
C₁₉H₁₇N₅O

Guidance literature:: Multi-step reaction with 3 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium carbonate / 1,2-dimethoxyethane; N,N-dimethyl-formamide / 130 - 170 °C / Microwave irradiation

2: Oxone / water; ethyl acetate

3: 1,4-dioxane / Reflux

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; Oxone; potassium carbonate; In 1,4-dioxane; 1,2-dimethoxyethane; water; ethyl acetate; N,N-dimethyl-formamide; 1: Suzuki coupling;
DOI:10.1016/j.bmcl.2012.01.041