化工社化工社 化学情報印刷レポート · 研究参考用
5-bromomethylene-10,11-dihydro-5H-dibenzo[a,d]cycloheptene → N-[3-(10,11-Dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-2-methyl-phenyl]-methanesulfonamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-bromomethylene-10,11-dihydro-5H-dibenzo[a,d]cycloheptene | HCID 5257940 | — |
| 反応物 | N-[2-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanesulfonamide | HCID 58613440 | — |
| 生成物 | N-[3-(10,11-Dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-2-methyl-phenyl]-methanesulfonamide | HCID 59769895 | 13.2% |
反応手順
Following the procedures essentially as described in Example 219, below, and using N-[2-methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-methanesulfonamide (120 mg, 0.386 mmol) and 5-bromomethylene-10,11-dihydro-5H-dibenzo[a,d]cycloheptene (100 mg, 0.351 mmol), purification by UV-guided semi-preparatory reverse-phase HPLC affords 18 mg (13%) of the title compound as a yellow oil. MS (ES) 407 M+NH4), 388 (M−H); HPLC shows 96% purity.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07411072B2 |
| 出典データセット | uspto-grants-2008_08 |
| ORD ID | ord-0ef03af8d4414d6a8244f0a33dbcaed7 |
| 出典メモ | uspto-grants-2008_08 |