HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium iodide → HCID 58423880, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium iodide | HCID 25487 | — |
| Reactant | Ethanol, reaction products with ammonia, distn. residues | HCID 22020343 | — |
| Reactant | HCID 58423900 | HCID 58423900 | — |
| Product | HCID 58423880 | HCID 58423880 | 107.9% |
Reaction Steps
A solution of 6-bromo-1′-methyl-2′-(methylthio)-2-(tetrahydro-2H-pyran-3-yl)spiro[chroman-4,4′-imidazol]-5′(1′H)-one (20 mg, 0.047 mmol), NH4I (54.5 mg, 0.37 mmol) in a solution of NH3/EtOH (2 mL, 8 N) was heated at 120° C. in a tube in a microwave reactor for 3 h. After cooling, the mixture was concentrated in vacuo to give 2′-amino-6-bromo-1′-methyl-2-(tetrahydro-2H-pyran-3-yl)spiro[chroman-4,4′-imidazol]-5′(1′H)-one (20 mg, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450308B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-cddc47ab50f440e4a11c18ae55edc180 |
| Source note | uspto-grants-2013_05 |