HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 5-Iodo-N-(phenylmethyl)imidazo[2,1-b]-1,3,4-thiadiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 5-Iodo-2-(methanesulfinyl)imidazo[2,1-b][1,3,4]thiadiazole | HCID 67109008 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Iodo-N-(phenylmethyl)imidazo[2,1-b]-1,3,4-thiadiazol-2-amine | HCID 58285397 | 80.8% |
Reaction Steps
5-Iodo-2-methanesulfinyl-imidazo[2,1-b][1,3,4]thiadiazole (500.00 mg; 1.60 mmol; 1.00 eq.) was dissolved in dichloromethane (1.60 ml) and benzylamine (622.18 μl; 4.79 mmol; 3.00 eq.) was added. Then, the reaction was refluxed overnight. The reaction was concentrated in vacuo. Then, 5 ml of isopropanol were added and the suspended solution was heated under reflux for 15 min. The mixture was allowed to cool to room temperature and then cooled to 0° C. After 15 min at 0° C., the solid was filtered and washed with isopropanol to give a white solid. The solid was dried at 60° C. for 1 h to give 460.2 mg of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08389554B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-5812b330eef54daf9d7f5983b9732bf7 |
| Source note | uspto-grants-2013_03 |