HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(2-Aminoethyl)-2-[[3-[4-(5-chloro-2-methoxyphenyl)-piperazin-1-yl]propyl]amino]pyrazine-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 19934801 | HCID 19934801 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(2-Aminoethyl)-2-[[3-[4-(5-chloro-2-methoxyphenyl)-piperazin-1-yl]propyl]amino]pyrazine-5-carboxamide | HCID 19934802 | — |
Reaction Steps
2 g (0.00365 mol) of 1,1-dimethylethyl 2-[[[2-[[3-[4-(5-chloro-2-methoxyphenyl)piperazin-1-yl]propyl]amino]pyrazin-5-yl]carbonyl]amino]ethylcarbamate are introduced into 10 ml of water in a 0.25 l round-bottomed flask and then 10 ml of concentrated hydrochloric acid are introduced dropwise. The mixture is cooled to 0° C. with an ice/salt/water mixture and 30% sodium hydroxide solution is added portionwise until the pH is basic. Extraction is carried out with dichloromethane, the organic phase is dried over sodium sulphate, filtered and the solvents are evaporated under reduced pressure and 1.32 g (0.00295 mol) of amorphous solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420130 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-079a58c975544c10ace8e00e473130d2 |
| Source note | uspto-grants-1995_05 |