HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrrolidine → HCID 10760148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 4-amino-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide | HCID 10852711 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10760148 | HCID 10760148 | 63.1% |
Reaction Steps
0.314 g (0.001 mol) of 4-amino-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide and 2.5 ml (0.15 mol) of pyrrolidine were stirred in 20 ml of ethanol in an autoclave at 130° C. for 4 hours. The reaction mixture was freed from solvent, the residue was suspended in 5 ml of ethanol and treated in an ultrasound bath for 15 min. The precipitate was filtered off, dissolved in 150 ml of 1N NaOH and filtered. The filtrate was adjusted to pH 6 with 1N HCl. The precipitate was filtered off under suction, washed with water and dried. There was obtained 0.22 g (63%) of 4 -amino-N-(2-methylamino-6-pyrrolidin-1-yl-pyrimidin-4-yl)-benzenesulfonamide as beige crystals; m.p.: >300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06030976 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-71b9a28dd77942ddb15fdf5ed872f699 |
| Source note | uspto-grants-2000_02 |