HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Chloro-4-(4-formylpiperazino)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichloropyrimidine | HCID 77531 | — |
| Reactant | 1-Piperazinecarboxaldehyde | HCID 82191 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Chloro-4-(4-formylpiperazino)pyrimidine | HCID 13869570 | 31.5% |
Reaction Steps
1-Formylpiperazine (38.5 g) and triethylamine (34 g) in ethanol (500 ml) were added slowly to a stirred solution of 2,4-dichloropyrimidine (50 g) in ethanol (2.5 ml) at room temperature. The mixture was stirred at room temperature for 24 hours then evaporated in vacuo and the residue partitioned between chloroform and water. The organic phase was washed with water and the combined aqueous phases extracted with chloroform. The combined chloroform extracts were dried (Na2SO4), evaporated in vacuo and the residue was crystallized twice from ethyl acetate to give 2-chloro-4-(4-formylpiperazino)pyrimidine, (24 g), m.p. 125°-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04483859 |
| Source dataset | uspto-grants-1984_11 |
| ORD ID | ord-b7a94321cbfc400694dc368fc88f9c81 |
| Source note | uspto-grants-1984_11 |