Dimethylamine → HCID 13208960、化合物
反応式
[F:1][C:2]1[CH:23]=[C:22]([F:24])[CH:21]=[CH:20][C:3]=1[O:4][C:5]1[CH:13]=[C:12]2[C:8]([CH2:9][CH2:10][CH:11]2O)=[CH:7][C:6]=1[NH:15][S:16]([CH3:19])(=[O:18])=[O:17].P(Cl)(Cl)(Cl)(Cl)[Cl:26].[CH3:31][NH:32][CH3:33]>ClCCl.C(OCC)C.ClCCl>[ClH:26].[F:1][C:2]1[CH:23]=[C:22]([F:24])[CH:21]=[CH:20][C:3]=1[O:4][C:5]1[CH:13]=[C:12]2[C:8]([CH2:9][CH2:10][CH:11]2[N:32]([CH3:33])[CH3:31])=[CH:7][C:6]=1[NH:15][S:16]([CH3:19])(=[O:18])=[O:17]参加物
6
実験手順
2.84 g of N-[6-(2,4-difluorophenoxy)-1-hydroxy-5-indanyl]methanesulfonamide and 1.83 g of phosphorus pentachloride are stirred in 50 ml of dichloromethane-diethyl ether (1:1) for 45 minutes at 0° C. At 0° C., a solution of 7 g of dimethylamine in 25 ml of dichloromethane is added to the reaction mixture. After 2 hours at 20° C. and 20 minutes of boiling, the mixture is concentrated and the residue is recrystallized from aqueous hydrochloric acid, yielding 2.41 g of N-[6-(2,4-difluorophenoxy)-1-dimethylamino-5-indanyl]methanesulfonamide, hydrochloride, mp 195° C.
後処理
- custom20 minutes
- concentrationthe mixture is concentrated
- customthe residue is recrystallized from aqueous hydrochloric acid
出典と根拠
- ORDレコード
- ord-161c7797c8854fe1a6d91047e0d56461
- 出典データセット
- uspto-grants-1985_11
- 特許番号
- US04555406
反応ノート
読み込み中…