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Triethylamine → 7-Bromo-6-methoxy-1(2H)-isoquinolinone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| 反応物 | 4-Bromo-3-methoxycinnamic acid | HCID 58005127 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 7-Bromo-6-methoxy-1(2H)-isoquinolinone | HCID 58005125 | 59.9% |
反応手順
A portion of the product from Step 1 (12.5 g, 48.6 mmol) was azeotroped with benzene and suspended 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 mixture was filtered through a pad of silica and eluted with ˜1 L of PhMe, the volatiles evaporated, the residue 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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08138164B2 |
| 出典データセット | uspto-grants-2012_03 |
| ORD ID | ord-74128ac1381148d3b10bfcc136020e48 |
| 出典メモ | uspto-grants-2012_03 |