HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyn-2-one → Bis(1,1-Dimethylethyl) 2-{3-[(ethyloxy)carbonyl]-6-methyl-2-pyridinyl}-1,4-piperazinedicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyn-2-one | HCID 15018 | — |
| Reactant | Bis(1,1-Dimethylethyl) 2-[(1Z)-1-amino-3-(ethyloxy)-3-oxo-1-propen-1-yl]-1,4-piperazinedicarboxylate | HCID 70556570 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Bis(1,1-Dimethylethyl) 2-{3-[(ethyloxy)carbonyl]-6-methyl-2-pyridinyl}-1,4-piperazinedicarboxylate | HCID 68176488 | 59.6% |
Reaction Steps
To a solution of bis(1,1-dimethylethyl) 2-[(1Z)-1-amino-3-(ethyloxy)-3-oxo-1-propen-1-yl]-1,4-piperazinedicarboxylate (may be prepared as described in Intermediate 4; 7.4 g) in ethanol (300 mL), was added 3-butyn-2-one (3.15 g) and the reaction was heated to reflux for 20 hours. The reaction mixture was evaporated and then partitioned between 2× EtOAc and water. The combined organic phases were washed with brine, dried through a hydrophobic frit, and then evaporated to a brown oil (8.54 g), which was purified by silica column (SP4-40M) eluting with 0-40% ethyl acetate in isohexane over 12CV. The clean fractions were combined and evaporated to give the title compound as a yellow oil (4.96 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933132B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-6c7b0824073c43a694beb0294dff5d5c |
| Source note | uspto-grants-2015_01 |