HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178448496, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (E)-6-iodo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione | HCID 68691018 | — |
| Reactant | HCID 68693777 | HCID 68693777 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178448496 | HCID 178448496 | — |
Reaction Steps
A mixture of (4E)-6-iodo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione (170 mg, 0.51 mmol) and 4-aminomethyl-1-butyl-1H-pyridin-2-one trifluoroacetate (150 mg, 0.51 mol) is stirred in dimethylformamide (2.7 mL) at room temperature in the presence of triethylamine (0.33 mL) for 18 hours. The reaction mixture is concentrated under reduced pressure. The residue is purified via semi-preparative HPLC (Prodigy ODS3 column, 5% acetonitrile/95% water/0.01% trifluoroacetic acid to 100% acetonitrile at 10 mL/min) to give (4Z)-6-iodo-4-({[(1-butyl-2-oxo-1,2-dihydropyridin-4-yl)methyl]amino}methylene)isoquinoline-1,3(2H,4H)-dione as an peach colored solid (25 mg, 10% due to substantial loss of material during HPLC malfunction).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-5f0e5ec865b74a9bbe007928a3a7b8b7 |
| Source note | uspto-grants-2010_05 |