HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 5-Aziridin-1-yl-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-yhnethyl)-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Chloro-5-(2-chloroethyl)amino-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)benzamide | HCID 11417653 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Aziridin-1-yl-2-chloro-N-(tricyclo[3.3.1.13,7]dec-1-yhnethyl)-benzamide | HCID 20670052 | 17% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
2-Chloro-5-(2-chloroethyl)amino-N-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-benzamide (0.15 g), cesium carbonate (0.192 g) and acetonitrile (3 ml) were combined and heated in a sealed tube at 100° C. for 24 hours. The cooled reaction mixture was poured into water (50 ml) and the product extracted into ethyl acetate, dried over magnesium sulphate, filtered and concentrated under reduced pressure. The crude product was purified by NPHPLC eluting with 0-5% ethanol in dichloromethane to give the title compound as a white solid (0.023 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06201024B1 |
| Source dataset | uspto-grants-2001_03 |
| ORD ID | ord-6edbd64372434046b8f795b328408452 |
| Source note | uspto-grants-2001_03 |