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2-FURAN-2-YL-IMIDAZO[1,2-A]PYRIDINE, also known as LGD-2226, is a chemical compound with potential pharmacological properties. It belongs to the class of imidazo[1,2-a]pyridine derivatives and has been investigated for its potential therapeutic uses in cancer treatment and immunomodulation. Studies have shown that 2-FURAN-2-YL-IMIDAZO[1,2-A]PYRIDINE exhibits antiproliferative and pro-apoptotic effects on cancer cells, making it a promising candidate for drug development in the field of oncology. Additionally, its immunomodulatory properties suggest that it may have potential applications in the treatment of autoimmune and inflammatory diseases. Further research is ongoing to explore the full range of pharmacological activities and potential therapeutic uses of 2-FURAN-2-YL-IMIDAZO[1,2-A]PYRIDINE.

28795-36-0

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28795-36-0 Usage

Uses

Used in Oncology:
2-FURAN-2-YL-IMIDAZO[1,2-A]PYRIDINE is used as an anticancer agent for its antiproliferative and pro-apoptotic effects on cancer cells. It has potential therapeutic uses in the treatment of various types of cancer.
Used in Immunomodulation:
2-FURAN-2-YL-IMIDAZO[1,2-A]PYRIDINE is used as an immunomodulatory agent for its potential applications in the treatment of autoimmune and inflammatory diseases. Its immunomodulatory properties are currently being explored for their therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 28795-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,9 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28795-36:
(7*2)+(6*8)+(5*7)+(4*9)+(3*5)+(2*3)+(1*6)=160
160 % 10 = 0
So 28795-36-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H8N2O/c1-2-6-13-8-9(12-11(13)5-1)10-4-3-7-14-10/h1-8H

28795-36-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(furan-2-yl)imidazo[1,2-a]pyridine

1.2 Other means of identification

Product number -
Other names 2-(2-furyl)imidazolo[1,2-a]pyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:28795-36-0 SDS

28795-36-0Relevant academic research and scientific papers

Liquid-phase organic synthesis of imidazo[1,2-a]pyridine derivatives using PEG-supported sulfonyl chloride

Wang, Chao-Li,Sheng, Shou-Ri.,Chen, Hu,Liu, Xiao-Ling,Cai, Ming-Zhong

, p. 289 - 291 (2008)

Reaction of PEG-bound sulfonic acid with thionyl chloride formed the difunctionalised PEG-supported sulfonyl chloride, which was treated with α-hydroxyketones, followed by treatment with 2-aminopyridine in the presence of potassium carbonate efficient to afford imidazo[1,2-a]pyridines in good yields with a facile work-up procedure.

A multi pathway coupled domino strategy: I2/ TBHP-promoted synthesis of imidazopyridines and thiazoles via sp3, sp2 and sp C-H functionalization

Feng, Lei,Li, Shichen,Ma, Chen,Wang, Xinfeng,Wang, Yishou,Yao, Yiming

, p. 5919 - 5927 (2022/03/31)

I2/TBHP-promoted, one-pot, multi pathway synthesis of imidazopyridines and thiazoles has been achieved through readily available ethylarenes, ethylenearenes and ethynearenes. I2/TBHP as an initiator and oxidant is used to realize the C-H functionalization of this domino reaction. Simple and available starting materials, wide range of functional group tolerance, high potential for drug activity of the products and application in production are the advantageous features of this method.

Synthetic method of imidazopyridine compounds

-

Paragraph 0054-0067, (2021/03/24)

The invention provides a novel method for synthesizing imidazopyridine compounds. According to the invention, aminopyridine compounds and sulfur ylide are used as original reaction substrates, iron phthalocyanine (FeIIPc) is used as a catalyst, and a series of the imidazopyridine compounds are obtained under the condition that the advantages of mildness, greenness, high efficiency, wide substrateuniversality and the like are achieved.

Molecular iodine enabled generation of iminyl radicals from oximes: A facile route to imidazo[1,2-a]pyridines and its regioselective C-3 sulfenylated products from simple pyridines

Singh, Deepak,Chowdhury, Soumyadeep Roy,Pramanik, Shyamal,Maity, Soumitra

, (2021/04/22)

An iodine promoted simple and environment friendly protocol has been developed to access imidazo[1,2-a]pyridines from unfunctionalized pyridines and oxime esters. This straightforward method efficiently converts the substrates into corresponding products affording moderate to good yields with large functional group tolerance. Additionally extensive investigation revealed that regioselective domino C-3 methyl sulfenylated imidazo[1,2-a]pyridines were also accessible first time from pyridines and oxime esters in DMSO solvent. The reaction operates through metal-free generation of iminyl radicals from easily accessible oxime esters, to build up the second heterocyclic ring on pyridines.

A simple and efficient route to 2-arylimidazo[1,2-a]pyridines and zolimidine using automated grindstone chemistry

Das, Dharmendra,Bhutia, Zigmee T.,Panjikar, Padmini C.,Chatterjee, Amrita,Banerjee, Mainak

supporting information, p. 4099 - 4107 (2020/09/09)

A green and efficient mechanochemical method for the synthesis of a series of 2-arylimidazo[1,2-a]pyridines was developed using an electrical grinder. I2 catalyzed mechanochemical grinding facilitates the cyclocondensation reaction between various aryl methyl ketones and 2-aminopyridines to afford 2-arylimidazo[1,2-a]pyridines in good yields at ambient temperature. The method was successfully used for the gram-scale synthesis of a marketed drug, zolimidine. The noticeable advantages of this environmentally sustainable protocol include mild conditions, simple instrumentation, inexpensive catalyst, atom economy, short reaction time etc.

Electrochemically initiated intermolecular C-N formation/cyclization of ketones with 2-aminopyridines: An efficient method for the synthesis of imidazo[1,2-: A] pyridines

Feng, Mei-Lin,Li, Shu-Qi,He, Hui-Zi,Xi, Long-Yi,Chen, Shan-Yong,Yu, Xiao-Qi

supporting information, p. 1619 - 1624 (2019/04/08)

Electrochemical intermolecular C-N formation/cyclization of ketones with 2-aminopyridines using catalytic hydriodic acid as the redox mediator was developed, providing imidazo[1,2-a]pyridines under more environmentally benign conditions. The reaction proceeds in a simple undivided cell, using low toxic ethanol as the solvent, without external oxidants, and exhibits high atom economy. A variety of ketones including acetophenones, unsatruated and alkyl ketones are amenable to this reaction, affording the corresponding products in moderate to excellent yields. A three-component tandem reaction realizing C-N, C-S/C-Se bond formation can also be achieved under standard conditions.

Iodine mediated oxidative cross coupling of 2-aminopyridine and aromatic terminal alkyne: A practical route to imidazo[1,2-: A] pyridine derivatives

Samanta, Surya Kanta,Bera, Mrinal K.

, p. 6441 - 6449 (2019/07/10)

A novel, transition-metal free route leading to imidazo[1,2-a]pyridine derivatives via iodine mediated oxidative coupling between 2-aminopyridine and aromatic terminal alkyne has been demonstrated. This newly developed method discloses an operationally simple way for the construction of imidazoheterocycles. Commercially available antiulcer drug zolimidine may readily be synthesized employing this method.

Easy and efficient selenocyanation of imidazoheterocycles using triselenodicyanide

Redon, Sébastien,Obah Kosso, Anne Roly,Broggi, Julie,Vanelle, Patrice

supporting information, p. 2771 - 2773 (2017/06/23)

The regioselective selenocyanation of imidazoheterocycles using triselenodicyanide at room temperature is reported. The electrophilic aromatic substitution of a broad range of substrates is promoted by the triselenodicyanide obtained by oxidative coupling

Au-catalyzed domino process synthesis of imidazo[1,2-a]pyridines from 2-aminopyridine and N-tosylhydrazones: An efficient C[sbnd]N bond formation reaction

Guo, Pengfeng,Huang, Shuyu,Mo, Jiaxian,Chen, Xiaoyan,Jiang, Hangqi,Chen, Weifeng,Cai, Hehuan,Zhan, Haiying

, p. 43 - 46 (2016/11/25)

A novel Au-catalyzed domino reaction for the synthesis of imidazo[1,2-a]pyridines from 2-aminopyridine and N-tosylhydrazones has been developed using molecular oxygen. It represents a new strategy for the formation of C[sbnd]N bonds. This transformation demonstrated a broad tolerance toward the substrates and allowed the generation of a diverse imidazo[1,2-a]pyridine derivatives with good yields.

Highly Efficient and Practical Thiocyanation of Imidazopyridines Using an N-Chlorosuccinimide/NaSCN Combination

Zhang, Hailei,Wei, Qian,Wei, Shiqiang,Qu, Jingping,Wang, Baomin

, p. 3373 - 3379 (2016/07/23)

A direct C–H thiocyanation of imidazo[1,2-a]pyridines, and a practical sequential one-pot condensation/C–H thiocyanation process, using a combination of N-chlorosuccinimide/NaSCN for the synthesis of 3-thiocyanatoimidazo[1,2-a]pyridines have been develope

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