HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Cyclopentyl-6-(1-piperazinyl)-2-pyrimidinamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 4-Chloro-6-cyclopentylpyrimidin-2-amine | HCID 21846367 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-Cyclopentyl-6-(1-piperazinyl)-2-pyrimidinamine | HCID 24798144 | 18.1% |
Reaction Steps
A solution of crude 2-amino-4-chloro-6-cyclopentylpyrimidine (150 mg, 0.76 mmol), N-BOC piperazine (184 mg, 0.99 mmol) and Et3N (210 uL, 1.5 mmol) in EtOH (2 mL) was heated at 70° C. for 16 h. The reaction was cooled to rt and concentrated and the crude residue purified (2 M NH3 in MeOH/CH2Cl2) to yield a white solid (34 mg, 11%). MS (ESI): mass calcd. for C18H29N5O2, 347.2; m/z found, 348.3 [M+H]+. 1H NMR (MeOD): 6.01 (s, 1H), 3.66-3.58 (m, 4H), 3.53-3.43 (m, 4H), 3.33 (td, J=3.3, 1.6, 1H), 2.90-2.75 (m, 1H), 2.05-1.90 (m, 2H), 1.87-1.77 (m, 2H), 1.77-1.62 (m, 4H), 1.53-1.46 (m, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07923451B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-7915622ae4624d508fb4076d5da9a5b1 |
| Source note | uspto-grants-2011_04 |