HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 3-[4-(3,4-dimethoxyphenyl)-4-isopropyl-4-cyanobutyl]-6,7-dimethoxy-N-methyl-3,4-dihydroisoquinolinium iodide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 3-[4-(3,4-Dimethoxyphenyl)-4-isopropyl-4-cyanobutyl]-6,7-dimethoxy-3,4-dihydroisoquinoline | HCID 20202182 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-[4-(3,4-dimethoxyphenyl)-4-isopropyl-4-cyanobutyl]-6,7-dimethoxy-N-methyl-3,4-dihydroisoquinolinium iodide | HCID 20202211 | — |
Reaction Steps
The dihydroisoquinoline derivative of formula 40 is then N-alkylated using a compound of formula R3 -L to produce a 3,4-dihydroisoquinolinium derivative of formula 41 (step 2). For example, 3-[4-(3,4-dimethoxyphenyl)-4-isopropyl-4-cyanobutyl]-6,7-dimethoxy-3,4-dihydroisoquinoline (40) is dissolved in acetone with methyl iodide and heated at reflux to produce 3-[4-(3,4-dimethoxyphenyl)-4-isopropyl-4-cyanobutyl]-6,7-dimethoxy-N-methyl-3,4-dihydroisoquinolinium iodide (41).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04667038 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-f3a40d44b9b749baadba927633af2ef0 |
| Source note | uspto-grants-1987_05 |