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 [(2E)-3-(4-bromo-3-methoxyphenyl)acrylic acid](12.5 g, 48.6 mmol) was azeotroped with benzene and suspended in benzene (94 mL). Triethylamine (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 h. The mixture was filtered through a pad of silica and eluted with ˜1 L of toluene, the volatiles evaporated, the residue resuspended in diphenylmethane (94 mL) and the mixture heated to reflux for three 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 | US08278322B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-303eae82c25440e5b034011d6793065f |
| Source note | uspto-grants-2012_10 |