HuagongsheHuagongshe Chemistry Print Report · For research reference only
O,O-Dipyridin-2-yl carbonothioate → HCID 12049865, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O,O-Dipyridin-2-yl carbonothioate | HCID 719784 | — |
| Reactant | HCID 12049864 | HCID 12049864 | — |
| Reactant | 3-Chloro-1,3-dihydro-4-isothiocyanato-2H-indol-2-one | HCID 22461250 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12049865 | HCID 12049865 | 96% |
Reaction Steps
3-Chloro-4-isothiocyanatooxindole. 4-Dimethylaminopyridine (0.031 g, 0.256 mmol) and di-2-pyridyl thionocarbonate (0.983 g, 4.23 mmol) are added to a solution of 4-amino-3-chloroindole (0.655 g, 2.82 mmol) in methylene chloride. The resulting mixture is stirred at room temperature for 1 hour. The volatile organics are removed by rotary evaporation and the crude residue is purified via silica gel column chromatography using 20% ethyl acetate/hexanes as the eluent. The appropriate fractions are combined and the solvents removed by rotary evaporation to yield 0.511 g of 3-chloro-4-isothiocyanatoindole as a yellow solid (96%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06395764B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-6f89d4fc88e942259119eacbccc82bc5 |
| Source note | uspto-grants-2002_05 |