Dichloromethane methanol → (RS)-S-Methyl-S-[3-({[4-(thiazol-2-ylamino)quinazolin-7-yl]amino}methyl)-phenyl]sulphoximide
反応式
C(OC([N:6]=[S:7]([CH3:33])([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH2:15][NH:16][C:17]2[CH:26]=[C:25]3[C:20]([C:21]([NH:27][C:28]4[S:29][CH:30]=[CH:31][N:32]=4)=[N:22][CH:23]=[N:24]3)=[CH:19][CH:18]=2)[CH:10]=1)=[O:8])=O)C.ClCCl.CO>CO>[CH3:33][S:7]([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([CH2:15][NH:16][C:17]2[CH:26]=[C:25]3[C:20]([C:21]([NH:27][C:28]4[S:29][CH:30]=[CH:31][N:32]=4)=[N:22][CH:23]=[N:24]3)=[CH:19][CH:18]=2)[CH:10]=1)(=[NH:6])=[O:8]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
According to GWP 6, the conversion of (RS)-N-(ethoxycarbonyl)-S-methyl-S-[3-({[4-(thiazol-2-ylamino)quinazolin-7-yl]amino}methyl)phenyl]sulphoximide (40 mg, 0.083 mmol) and chromatographic purification (silica gel, dichloromethane/methanol: 0→20% methanol) gives the desired product in 77% yield (26 mg).
出典と根拠
- ORDレコード
- ord-84bd8c8c80644c9cafa754f9157d2ce6
- 出典データセット
- uspto-grants-2011_01
- 特許番号
- US07863283B2
反応ノート
読み込み中…