関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylethylamine | HCID 81531 | — |
| 反応物 | Propylphosphonic anhydride | HCID 111923 | — |
| 反応物 | 5-Bromo-2-methylbenzoic acid | HCID 346004 | — |
| 反応物 | Benzoic acid, 4-amino-3,5-dimethyl-, methyl ester | HCID 11030398 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Methyl 4-[(5-bromo-2-methyl-benzoyl)amino]-3,5-dimethyl-benzoate | HCID 86707323 | 107.9% |
反応手順
To a solution of 5-bromo-2-methylbenzoic acid (2.0 g, 0.008 mol) in CH2Cl2 (20 mL) at 0° C. are added methyl 4-amino-3,5-dimethylbenzoate (1.28 g, 0.0072, see preparation 12) and N,N-diisopropylethylamine (4.12 g, 0.032 mol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 7.63 g, 0.024 mol) is added via syringe and stirred at 50° C. After 16 hours, the solvent is removed under reduced pressure and the residue is diluted with water and extracted twice with ethyl acetate. The organic layers are combined and dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) using 12% ethyl acetate in hexane to give the title compound as a white solid (2.9 g, 97%). Mass spectrum (m/z): 376.0 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US08933098B2 |
|---|
| 出典データセット | uspto-grants-2015_01 |
|---|
| ORD ID | ord-3884e0580ecd49ed9584e5f0e80cfee7 |
|---|
| 出典メモ | uspto-grants-2015_01 |
|---|