HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178483974, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-{[2-(Dimethylamino)ethyl]sulfanyl}aniline | HCID 43299439 | — |
| Reactant | (E)-6-bromo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione | HCID 68692760 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178483974 | HCID 178483974 | 65% |
Reaction Steps
(4E)-6-Bromo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione (0.21 g, 0.76 mmol) and 4-(2-dimethylamino-ethylsulfanyl)-phenylamine (0.15 g, 0.76 mmol) were stirred in N,N-dimethylformamide (5 mL) and triethylamine (0.3 mL) at 60-70° C. for 5 minutes and then at room temperature for 10 minutes. The reaction mixture is quenched by the addition of water. The solid material is then collected, washed with diethyl ether, water, and methanol, and then dried under vacuum to give (4Z)-6-bromo-4-{[(4-{[2-(dimethylamino)ethyl]thio}phenyl)amino]methylene}isoquinoline-1,3(2H,4H)-dione (0.22 mg, 65%) as a golden powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-821a714a3a614d2cb625109d52a93874 |
| Source note | uspto-grants-2010_05 |