HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 23044936, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 4-Amino-N-(1-azabicyclo[2.2.2]octan-3-yl)-5-chloro-2-(cyclopropylmethoxy)benzene-1-carboximidic acid | HCID 71342 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 23044936 | HCID 23044936 | 79.3% |
Reaction Steps
To a solution of N-(1-azabicyclo[2.2.2]oct-3-yl)-2-cyclopropylmethoxy-4-amino-5-chlorobenzamide (3.5 g; 0.01 mol) in acetone (200 ml), iodomethane (2.8 g; 0.02 moles) was added and the resulting mixture stirred to room temperature for 20 hours. The precipitated solid was collected, washed with acetone and dried to give N-(1-azabicyclo[2.2.2]oct-3-yl)-2-cyclopropylmethoxy-4-amino-5-chlorobenzamide methyl iodide (3.9 g), m.p. 274°-276° C. (d) (after recrystallisation from a mixture of acetonitrile and water).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04937236 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-225c71a2b6494669a2eb42d333d38f53 |
| Source note | uspto-grants-1990_06 |