HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-methyl-2-pyrrolidone → HCID 60045645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 22273362 | HCID 22273362 | — |
| Reactant | HCID 22273418 | HCID 22273418 | — |
| Product | HCID 60045645 | HCID 60045645 | — |
Reaction Steps
1,1-Dimethylethyl, 4-(4-quinazolinyl)-3,5-dimethylpiperazine-1-carboxylate 4-Chloroquinazoline (6 g), cis-1,1-diethylethyl, 3,5-dimethylpiperazine-1-carboxylate (7.8 g), N,N-diisopropylethylamine (32 ml) in 1-methyl-2-pyrrolidinone (70 ml) were heated at 120° C. for 6 days under nitrogen. The mixture was partitioned between ethyl acetate and brine. The organic phase collected and further washed with brine (×2), collected, dried (MgSO4) and solvent evaporated under reduced pressure to leave a pale brown solid. Purification was by silica gel chromatograpy eluting with ethyl acetate/iso-hexane (3:7) to give the subtitle compound as a pale yellow oil. Yield: 1.1 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06969713B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-a400d6f183ce473391475dadd88e6a2a |
| Source note | uspto-grants-2005_11 |