89786-54-9

Usage

Uses

Due to the limited information available on Thiazolo[4,5-c]pyridin-2-amine, specific uses in different industries cannot be accurately listed. However, given its classification as a benzimidazole, it is reasonable to infer that it may have potential applications similar to other compounds in this class. These applications may include, but are not limited to:
1. Used in Pharmaceutical Industry:
Thiazolo[4,5-c]pyridin-2-amine could be used as a pharmaceutical intermediate or a potential drug candidate for the development of new medications. Benzimidazoles are known for their diverse biological activities, including antiparasitic, anthelmintic, and anticancer properties.
2. Used in Materials Science:
In the field of materials science, Thiazolo[4,5-c]pyridin-2-amine might be employed as a component in the synthesis of new materials with specific properties, such as conductivity, magnetism, or optical characteristics.
3. Used in Chemical Research:
As a lesser-known compound, Thiazolo[4,5-c]pyridin-2-amine could serve as a subject of study in chemical research, where its properties, reactivity, and potential applications can be further explored.

InChI:InChI=1/C6H5N3S/c7-6-9-4-3-8-2-1-5(4)10-6/h1-3H,(H2,7,9)

Upstream product

• 98130-83-7 3-nitro-4-thiocyanato-pyridine 
• 273-75-6 thiazolo[4,5-c]pyridine 
• 3425-46-5 potassium selenocyanate 
• 20511-15-3 3-amino-4-chloropyridine 
• 13091-23-1 4-chloro-3-nitropyridine 
• 17356-08-0 thiourea 
• 97249-84-8 N-(thiazolo[4,5-c]pyridin-2-yl)acetamide 
• 7647-01-0 hydrogenchloride 
• 7732-18-5 water 

Downstream Products

• 884860-63-3 2-chlorothiazolo[4,5-c]pyridine 
• 1311319-10-4 (S)-4-tert-butyl 1-((S)-1-(2-((Z)-3-butylthiazolo[4,5-c]pyridin-2(3H)-ylidenecarbamoyl)-4-(trifluoromethyl)phenoxy)propan-2-yl) 2-(tert-butoxycarbonylamino)succinate 
• 1311319-11-5 (3S)-4-({(1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl}oxy)-3-amino-4-oxobutanoic acid hydrochloride 
• 1311318-81-6 (1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl 2-methylalaninate 
• 1311319-03-5 (1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl 2-methylalaninate hydrochloride 
• 1311318-92-9 (2Z)-5-[4-(acetyloxy)-3,5-dimethylbenzyl]-3-butyl-2-{[2-{[(2S)-2-hydroxypropyl]oxy}-5-(trifluoromethyl)benzoyl]imino}-2,3-dihydro[1,3]thiazolo[4,5-c]pyridin-5-ium bromide 
• 1311319-06-8 dibenzyl (1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl phosphate 
• 1311319-02-4 (1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl N-(tert-butoxycarbonyl)-2-methylalaninate 
• 1311318-80-5 (2Z)-5-[(acetyloxy)methyl]-3-butyl-2-{[2-{[(2S)-2-hydroxypropyl]oxy}-5-(trifluoromethyl)benzoyl]imino}-2,3-dihydro[1,3]thiazolo[4,5-c]pyridin-5-ium bromide 
• 1311318-94-1 (1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl 2-(dimethylamino)ethylcarbamate 
• 1311318-93-0 4-({(1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl}oxy)-4-oxobutanoic acid 
• 1311318-91-8 N-[(2Z)-3-butyl-5-oxido[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]-2-{[(2S)-2-hydroxypropyl]oxy}-5-(trifluoromethyl)benzamide 
• 1311318-88-3 (1S)-2-[2-({[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]amino}carbonyl)-4-(trifluoromethyl)phenoxy]-1-methylethyl dihydrogen phosphate 
• 1311319-00-2 (2S)-1-[2-{[(2Z)-3-butyl[1,3]thiazolo[4,5-c]pyridin-2(3H)-ylidene]carbamoyl}-4-(trifluoromethyl)phenoxy]propan-2-yl acetate 

Relevant academic research and scientific papers

Iodine-catalyzed amination of benzothiazoles with KSeCN in water to access primary 2-aminobenzothiazoles

A facile and sustainable approach for the amination of benzothiazoles with KSeCN using iodine as the catalyst in water has been disclosed under transition-metal free conditions. The reaction proceeded smoothly to afford various primary 2-amino benzothiazoles in up to 96% yield. A series of control experiments were performed, suggesting a ring-opening mechanism was involved via a radical process. This protocol provides efficient synthesis of primary 2-aminobenzothiazoles

HETEROCYCLIC COMPOUNDS FOR MODULATING NR2F6

The present disclosure relates to compounds capable of modulating the activity of NR2F6. The compounds of the disclosure may be used in methods for the prevention and/or the treatment of diseases and disorders associated with modulating NR2F6 activity.

THIENOPYRIMIDINE COMPOUNDS

The present invention relates to the use of novel compounds of Formula I: wherein all variable substituents are defined as described herein, which are SYK inhibitors and are useful for the treatment of auto-immune and inflammatory diseases.

DERIVATlVES OF UREA AND RELATED DIAMINES, METHODS FOR THEIR MANUFACTURE AND USES THEREFOR

The present invention relates generally to compounds represented in Formula I, pharmaceutical compositions comprising them and methods of treating of diseases or disorders related to the function of the calcium sensing receptor. The invention also relates to processes for making such compounds and to intermediates useful in these processes

A single-step preparation of thiazolo[5,4-b]pyridine- and thiazolo[5,4-c]pyridine derivatives from chloronitropyridines and thioamides, or thioureas

(Chemical Equation Presented) A one-step synthesis of thiazolo[5,4-b] pyridines from an appropriately substituted chloronitropyridine and thioamide, or thiourea, is presented. In particular, the reaction was used to prepare a large number of 6-nitrothiazo