HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 58423762, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178423433 | HCID 178423433 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58423762 | HCID 58423762 | 90.3% |
Reaction Steps
NaH (5.3 mg, 0.131 mmol) is added to a solution of 2′-amino-6-bromo-2,2-dimethylspiro[chroman-4,4′-imidazol]-5′(3′H)-one (45 mg, 0.131 mmol) in THF (3 mL) at 0° C. under N2. The mixture is stirred for 1 h at room temperature. Then MeI (18.6 mg, 0.131 mmol) is added. The mixture is quenched with water and extracted with ethyl acetate. The organic layer is concentrated in vacuo. The residue is purified by preparative TLC to give 2′-amino-6-bromo-1′,2,2-trimethylspiro[chroman-4,4′-imidazol]-5′(1′H)-one (40 mg, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450308B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-0b62fa3b076d40f0b636a0fdece336ab |
| Source note | uspto-grants-2013_05 |