Thionyl Chloride → 3-(Chloromethyl)-8-methyl-2-o-tolylquinoline
反応式
[CH3:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[N:10]=[C:9]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH3:18])[C:8]([CH2:19]O)=[CH:7]2.O=S(Cl)[Cl:23]>C(Cl)(Cl)Cl>[Cl:23][CH2:19][C:8]1[C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH3:18])=[N:10][C:11]2[C:6]([CH:7]=1)=[CH:5][CH:4]=[CH:3][C:2]=2[CH3:1]参加物
4
実験手順
Prepared according to Procedure C using (8-methyl-2-o-tolylquinolin-3-yl)-methanol (670 mg, 2.5 mmol) and SOCl2 (0.91 mL, 5 eq) in CHCl3 (10 mL). After isolation, the resultant oil was carried on crude without purification for the next step.
後処理
- customPrepared
- customAfter isolation, the resultant oil was carried on crude without purification for the next step
出典と根拠
- ORDレコード
- ord-d6276ba642af47418dcbba960a738f46
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08193199B2
反応ノート
読み込み中…