HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → N,N-diethyl-4-[(3-methoxyphenyl)-(10-prop-2-enyl-9,10-diazatricyclo[4.2.1.12,5]decan-9-yl)methyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-[(9,10-diazatricyclo[4.2.1.12,5]dec-9-yl)-(3-methoxy phenyl)methyl]-N,N-diethylbenzamide | HCID 67237501 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | N,N-diethyl-4-[(3-methoxyphenyl)-(10-prop-2-enyl-9,10-diazatricyclo[4.2.1.12,5]decan-9-yl)methyl]benzamide | HCID 53258062 | 96% |
Reaction Steps
A mixture formed of the compound obtained in example 5.1 (0.98 mmoles), of allyl bromide (1.5 equivalents) and of anhydrous potassium carbonate (3 equivalents) in acetone (25 ml) is heated at reflux for 14 hours. At the end it is filtered and the filtrate is evaporated under vacuum. The compound 4-[(10-allyl-9,10-diazatricyclo[4.2.1.12,5]dec-9-yl)-(3-methoxyphenyl)methyl]-N,N-diethyl benzamide (light solid) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08609659B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-db60b76b1b5d4a69a73f33faddbae21d |
| Source note | uspto-grants-2013_12 |