HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloroaniline → 4-(3-Chloro-anilino)-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloroaniline | HCID 7932 | — |
| Reactant | 4-chloro-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine | HCID 22484442 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Product | 4-(3-Chloro-anilino)-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine | HCID 9905178 | — |
Reaction Steps
A suspension of 1.251 g (5.45 mmol) of 4-chloro-6-phenyl-7H-pyrrolo[2,3-d]pyrimidine and 1.15 ml (10.9 mmol) of 3-chloro-aniline in 20 ml of n-butanol and 0.5 ml of DMPU is heated at boiling for 2 hours. The reaction mixture is cooled and filtered. Stirring of the residue in hot THF/methanol yields the title compound; m.p. 285-286° C.; FAB-MS: (M+H)+ =321.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06140332 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-cc7c3d072056483bbd490e35c7107d83 |
| Source note | uspto-grants-2000_10 |