HuagongsheHuagongshe Chemistry Print Report · For research reference only
O,O-Dipyridin-2-yl carbonothioate → 4,7-Dimethyl-5-benzimidazolylisothiocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O,O-Dipyridin-2-yl carbonothioate | HCID 719784 | — |
| Reactant | 4,7-dimethyl-3H-benzimidazol-5-amine | HCID 18379861 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4,7-Dimethyl-5-benzimidazolylisothiocyanate | HCID 21472724 | — |
Reaction Steps
To a solution of di-2-pyridyl thionocarbonate (2.29 g) and 4-dimethylaminopyridine (0.03 g) in CH2Cl2 (150 mL) is added dropwise over 30 minutes a solution of 5-amino-4,7-dimethylbenzimidazole (0.816 g) in methanol (50 mL). The mixture is stirred for 3 hours at room temperature, then rotary evaporated. The residue is purified by flash chromatography on silica gel, eluting with a gradient of 50% to 80% ethyl acetate/hexane to afford 4,7-dimethyl-5-benzimidazolylisothiocyanate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541210 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-80e7db9e6e82480cb85c6b6cd20d3025 |
| Source note | uspto-grants-1996_07 |