HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308984Generated: October 25, 2026
N-3-Bromopropylphthalimide → N-[3-(N-phenyl-N-pyrid-2-ylamino)propyl]phthalimide
https://huagongshe.com/reaction/2308984
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-3-Bromopropylphthalimide | HCID 21611 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-2-Pyridylaniline | HCID 81130 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[3-(N-phenyl-N-pyrid-2-ylamino)propyl]phthalimide | HCID 20186606 | — |
Reaction Steps
A solution of 2-(N-phenylamino)pyridine (5.0 g) in DMSO (15 ml) was added to a suspension of sodium hydride (0.78 g) in DMSO (20 ml). The mixture was stirred and slowly heated under nitrogen to 85° C. After the evolution of hydrogen had ceased, the mixture was cooled to room temperature and a solution of N-(3-bromopropyl)phthalimide (7.88 g) in DMSO (15 ml) added dropwise. The mixture was allowed to stand overnight and then poured into water. The aqueous phase was made acid to a pH between 2 to 4 and extracted with ether. The extracts were dried (MgSO4), the ether evaporated and the residue crystallised from ethanol to give N-[3-(N-phenyl-N-pyrid-2-ylamino)propyl]phthalimide, 3.69 g (35%) m.p. 103°-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04692456 |
|---|
| Source dataset | uspto-grants-1987_09 |
|---|
| ORD ID | ord-ef1965a29c304b348a573de56f31640e |
|---|
| Source note | uspto-grants-1987_09 |
|---|