HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1'-Thiocarbonyldi-2(1H)-pyridone → 2-Isothiocyanato-6-methoxy-[1,2,4]triazolo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1'-Thiocarbonyldi-2(1H)-pyridone | HCID 853162 | — |
| Reactant | 6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine | HCID 46864066 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Isothiocyanato-6-methoxy-[1,2,4]triazolo[1,5-a]pyridine | HCID 57476552 | 44.4% |
Reaction Steps
To 6-methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine (0.3 g, 1.8 mmol) in dichloromethane (15 mL) was added 1,1′-thiocarbonyldi-2(1H)-pyridone (0.51 g, 2.2 mmol). The reaction was stirred at room temperature overnight, concentrated in vacuo and purified via flash chromatography yielding 2-isothiocyanato-6-methoxy-[1,2,4]triazolo[1,5-a]pyridine (166 mg, 0.8 mmol, 44% yield) as a white solid. 1H NMR (300 MHz, CDCl3) δ ppm 8.03 (1H, d, J=2.20 Hz), 7.54 (1H, d, J=9.88 Hz), 7.34 (1H, dd, J=9.51, 2.56 Hz), 3.88 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309577B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-c30a880185174780a0f41039dafb725e |
| Source note | uspto-grants-2012_11 |