HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 68593328, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 59291570 | HCID 59291570 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68593328 | HCID 68593328 | — |
Reaction Steps
To a solution of 1-azabicyclo[2.2.2]oct-3-ylmethyl (2-phenyl-3-thienyl)carbamate (100 mg) in EtOAc (2 mL) was added iodomethane (36 μL) at room temperature, followed by stirring for overnight. The reaction mixture was filtered, then concentrated under reduced pressure, and freeze-dried to obtain 1-methyl-3-({[(2-phenyl-3-thienyl)carbamoyl]oxy}methyl)-1-azoniabicyclo[2.2.2]octane iodide (88 mg) as a yellow amorphous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367696B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-ba8504a93653440d9fa9d9573e568491 |
| Source note | uspto-grants-2013_02 |