HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 3-(2-Amino-3-propyl-3,4-dihydro-quinazolin-6-yloxy)-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 3-(4-Amino-3-propylaminomethyl-phenoxy)-benzonitrile | HCID 58625114 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(2-Amino-3-propyl-3,4-dihydro-quinazolin-6-yloxy)-benzonitrile | HCID 58625063 | — |
Reaction Steps
A mixture of 3-(4-amino-3-propylaminomethyl-phenoxy)-benzonitrile (0.032 mol) in ethanol (400 mL) was stirred at room temperature, and cyanogen bromide (0.038 mol) was added, and then the reaction mixture was stirred and refluxed for 2 hours. After cooling, the precipitate was filtered off, washed with diisopropyl ether and dried to yield crude product as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383637B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-58fed401931749de9b0f5ca92aefa48a |
| Source note | uspto-grants-2013_02 |