HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Aminomethyl)-1-methylpyridin-2(1H)-one → HCID 178480332, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Aminomethyl)-1-methylpyridin-2(1H)-one | HCID 22061287 | — |
| Reactant | (E)-6-iodo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione | HCID 68691018 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178480332 | HCID 178480332 | 88% |
Reaction Steps
(4E)-6-iodo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione (130 mg, 0.40 mmol), 4-aminomethyl-1-methyl-1H-pyridin-2-one (55 mg, 0.40 mol) were coupled in N,N-dimethylformamide (2 mL) at room temperature. The reaction mixture is diluted with water and the precipitate is collected by Büchner filtration and then dried under house vacuum to give (4Z)-6-iodo-4-({[(1-methyl-2-oxo-1,2-dihydropyridin-4-yl)methyl]amino}methylene)isoquinoline-1,3(2H,4H)-dione as an orange solid (0.15 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-49d5d93f6cdc41d0a17a54da7a4c8299 |
| Source note | uspto-grants-2010_05 |