Thiazolo[4,5-c]pyridine-2-thiol

Thiazolo[4,5-c]pyridine-2-thiol Suppliers list
Company Name: SynAsst Chemical.  
Tel: 021-60343070
Email:
Company Name: Suzhou JingTong Pharmaceutical Co., Ltd.  
Tel: 13675155016
Email: tongtf110@sina.com
Company Name: Aikon International Limited  
Tel: 025-66113011 19370895928
Email: qzhang@aikonchem.com
Company Name: Suzhou Nuoouman Biological Technology Co., Ltd.  
Tel: 15026866316
Email: 180642609@qq.com
Company Name: Shanghai Xuerong Chemical Technology Co., LTD  
Tel: 18201727566
Email: 230497258@qq.com
Thiazolo[4,5-c]pyridine-2-thiol Basic information
Product Name:Thiazolo[4,5-c]pyridine-2-thiol
Synonyms:Thiazolo[4,5-c]pyridine-2-thiol;Thiazolo[4,5-c]pyridine-2(3H)-thione;[1,3]thiazolo[4,5-c]pyridine-2-thiol
CAS:65128-66-7
MF:C6H4N2S2
MW:168.24
EINECS:
Product Categories:
Mol File:65128-66-7.mol
Thiazolo[4,5-c]pyridine-2-thiol Structure
Thiazolo[4,5-c]pyridine-2-thiol Chemical Properties
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
Safety Information
MSDS Information
Thiazolo[4,5-c]pyridine-2-thiol Usage And Synthesis
Synthesis
3-Amino-4-chloropyridine

20511-15-3

Potassium ethylxanthate

140-89-6

Thiazolo[4,5-c]pyridine-2-thiol

65128-66-7

Synthesis of thiazolo[4,5-c]pyridine-2-thiol (68): 3-amino-4-chloropyridine (67, 1.0 g, 8.3 mmol) was dissolved in 15 mL of anhydrous N,N-dimethylformamide (DMF) under nitrogen protection. Potassium ethylxanthate (KSCSOEt, 2.0 g, 12.5 mmol) was added to this solution in batches. The reaction mixture was stirred at 95-100°C for 15 h. The progress of the reaction was monitored by thin layer chromatography (TLC, unfolding agent: 70% ethyl acetate/hexane) to confirm complete consumption of the raw material. Upon completion of the reaction, the reaction was quenched with 35 mL of ice water followed by the addition of 40 mL of 1 M hydrochloric acid (HCl). The mixture was continued to be stirred for 30 minutes, during which time a precipitate was generated. The precipitate was collected by filtration, washed with 250 mL of water and dried under vacuum over phosphorus pentoxide (P4O10) to afford the target product thiazolo[4,5-c]pyridine-2-thiol (68, 0.98 g, 70% yield).

References[1] Patent: WO2006/122156, 2006, A2. Location in patent: Page/Page column 145-146
[2] Advanced Synthesis and Catalysis, 2017, vol. 359, # 11, p. 1837 - 1843
Thiazolo[4,5-c]pyridine-2-thiol Preparation Products And Raw materials
Raw materials3-Amino-4-chloropyridine-->Potassium ethylxanthate-->N,N-Dimethylformamide-->Hydrochloric acid
Preparation Products2-(Methylthio)thiazolo[4,5-c]pyridine
Tag:Thiazolo[4,5-c]pyridine-2-thiol(65128-66-7) Related Product Information
thiazolo[4,5-b]pyridine-2(3H)-thione THIAZOLO[5,4-B]PYRIDIN-2-AMINE Thiazolo[5,4-c]pyridine Thiazolo[4,5-c]pyridin-2-ol (5CI) Thiazolo[4,5-c]pyridin-2-amine 2-Mercaptobenzothiazole