HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178440612, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (4E)-6-t-butyl-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione | HCID 42625173 | — |
| Reactant | 4-aminomethyl-1-furan-3-yl-1H-pyridin-2-one hydrochloride | HCID 42625750 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178440612 | HCID 178440612 | 43% |
Reaction Steps
A mixture of (4E)-6-tert-butyl-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione (50 mg, 0.19 mmol), 4-aminomethyl-1-furan-3-yl-1H-pyridin-2-one hydrochloride (43 mg, 0.19 mmol), and triethylamine (150 μL, 1.1 mmol) in N,N-dimethylformamide (2 mL) is stirred overnight at room temperature. The reaction mixture is concentrated under reduced pressure, and the residue is triturated with chloroform to provide (4Z)-6-tert-butyl-4-[({[1-(3-furyl)-2-oxo-1,2-dihydropyridin-4-yl]methyl}amino)methylene]isoquinoline-1,3(2H,4H)-dione as a white solid (34 mg, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-18c373b4d6044471a7910f67fe442242 |
| Source note | uspto-grants-2010_05 |