HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-Amino-4-[4-(tert-butoxycarbonyl)piperazin-1-yl]-6-chloropyrimidine-5-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 2-Amino-4,6-dichloropyrimidine-5-carboxaldehyde | HCID 265546 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Amino-4-[4-(tert-butoxycarbonyl)piperazin-1-yl]-6-chloropyrimidine-5-carboxaldehyde | HCID 89407451 | — |
Reaction Steps
To a suspension of 2-amino-4,6-dichloropyrimidine-5-carboxaldehyde (3.84 g, 20 mmol) and DIPEA (5.2 mL, 30 mmol) in DMF was added tert-butyl piperazine-1-carboxylate (3.73 g, 20 mmol) portionwise. The reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated and the residue obtained was precipitated with H2O. The precipitate was collected, washed with water and dried in vacuo, to provide the title compound as a white solid in quantitative yield. MS (m/z) 342 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227984B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-92767fc64e594fd0889bf904dbe89207 |
| Source note | uspto-grants-2016_01 |