Thiazolo[4,5-c]pyridine-2-thiol
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
- Mol File:
- 65128-66-7.mol
Thiazolo[4,5-c]pyridine-2-thiol Chemical Properties
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
Thiazolo[4,5-c]pyridine-2-thiol Usage And Synthesis
Synthesis
20511-15-3
140-89-6
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
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