HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 21715697, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 18472312 | HCID 18472312 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21715697 | HCID 21715697 | — |
Reaction Steps
To a solution of (E)-N-[4-[N-methyl-N-(tetrahydro-pyran-4-yl)aminomethyl]phenyl]-3-[5-(4-isopropylphenyl)thiophen-2-yl]acrylamide (80 mg) in DMF (5 ml) was added at room temperature methyl iodide (0.04 ml), and the mixture was stirred for 3 days. Under reduced pressure, the solvent was evaporated, and to the residue was added acetonitrile. The resulting crystals were collected by filtration to give yellow crystals of N,N-dimethyl-N-[4-[[(E)-3-[5-(4-isopropylphenyl)thiophen-2-yl]-2-propenoyl]amino]benzyl]-4-tetrahydropyranyl ammonium iodide (Compound 280) (76.9 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06268354B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-bb071e57a85d463f9b7b0a278d918098 |
| Source note | uspto-grants-2001_07 |