HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-Bromo-6-methoxy-1(2H)-isoquinolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 4-Bromo-3-methoxycinnamic acid | HCID 58005127 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 7-Bromo-6-methoxy-1(2H)-isoquinolinone | HCID 58005125 | 59.9% |
Reaction Steps
A portion of the product from Step 1 (12.5 g, 48.6 mmol) was azeotroped with benzene and resuspended in benzene (94 mL). Et3N (9.49 mL, 68.1 mmol) and diphenylphosphoryl azide (10.48 mL, 48.6 mmol) were added, and the reaction mixture stirred at RT for 1 hour. The reaction mixture was then filtered through a pad of silica and eluted with ˜1 L of PhMe; the volatiles were evaporated; the residue was resuspended in diphenylmethane (94 mL); and the mixture heated to reflux for 3 hours (internal temperature 250° C.). The reaction mixture was allowed to cool to RT, stirred overnight, filtered and the solid washed with hexanes (100 mL) to give tan solid (7.4 g). LRMS ESI+ (M+H)+ 254.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08377874B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-919e903631084bfda8b1e0e10094874b |
| Source note | uspto-grants-2013_02 |