Oxalyl chloride → 8-chloro-3-[2-(4-morpholinyl)ethyl]-3H-imidazo[4,5-g]quinoline-7-carbonitrile
反応式
[N:1]1([CH2:7][CH2:8][N:9]2[C:21]3[C:12](=[CH:13][C:14]4[C:15](=O)[C:16]([C:22]#[N:23])=[CH:17][NH:18][C:19]=4[CH:20]=3)[N:11]=[CH:10]2)[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.C(Cl)(=O)C([Cl:28])=O>CN(C=O)C>[Cl:28][C:15]1[C:14]2[CH:13]=[C:12]3[N:11]=[CH:10][N:9]([CH2:8][CH2:7][N:1]4[CH2:6][CH2:5][O:4][CH2:3][CH2:2]4)[C:21]3=[CH:20][C:19]=2[N:18]=[CH:17][C:16]=1[C:22]#[N:23]参加物
実験手順
A suspension of 190.0 mg (0.59 mmol) of 3-[2-(4-morpholinyl)ethyl]-8-oxo-5,8-dihydro-3H-imidazo[4,5-g]quinoline-7-carbonitrile, 5.45 mL of 2M oxalyl chloride (in methylene chloride) and 5 drops of DMF is heated at reflux temperature for 1.5 hours. After cooling, the solvent is evaporated to dryness. The residue is cooled in an ice bath and neutralized to pH 7 by slow addition of ice-cooled, aqueous saturated sodium bicarbonate solution. The aqueous solution is extracted with methylene chloride. The organic phase is washed with cold brine and dried over sodium sulfate. Removal of the solvent in vacuo gives the crude product. Purification of the crude product by preparative TLC (developing solvent: 5:95 methanol/methylene chloride) gives 122.8 mg (61%) of the product as a yellow solid, mp 205–207° C.
後処理
- temperatureis heated
- temperatureat reflux temperature for 1.5 hours
- temperatureAfter cooling
- customthe solvent is evaporated to dryness
- temperatureThe residue is cooled in an ice bath
- additionneutralized to pH 7 by slow addition of ice-
- temperaturecooled
- extractionThe aqueous solution is extracted with methylene chloride
- washThe organic phase is washed with cold brine
- dry with materialdried over sodium sulfate
- customRemoval of the solvent in vacuo
- customgives the crude product
- customPurification of the crude product by preparative TLC (developing solvent: 5:95 methanol/methylene chloride)
出典と根拠
- ORDレコード
- ord-53d8e02a38614263aa14ea9ab05d59c8
- 出典データセット
- uspto-grants-2006_09
- 特許番号
- US07105531B2
反応ノート
読み込み中…