1-(Chloromethoxy)-2-methoxyethane → 10-Hexyl-3,7-dimethoxy-4-(2-methoxyethoxymethoxymethyl)-phenothiazine
反応式
[CH2:1]([N:7]1[C:20]2[CH:19]=[CH:18][C:17]([O:21][CH3:22])=[C:16]([CH:23]=[O:24])[C:15]=2[S:14][C:13]2[C:8]1=[CH:9][CH:10]=[C:11]([O:25][CH3:26])[CH:12]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[BH4-].[Li+].C(N1C2C=CC(OC)=C(CO)C=2SC2C1=CC=C(OC)C=2)CCCCC.C([Li])CCC.[CH3:60][O:61][CH2:62][CH2:63][O:64][CH2:65]Cl>O1CCCC1.C(OCC)C.CCCCCC>[CH2:1]([N:7]1[C:20]2[CH:19]=[CH:18][C:17]([O:21][CH3:22])=[C:16]([CH2:23][O:24][CH2:60][O:61][CH2:62][CH2:63][O:64][CH3:65])[C:15]=2[S:14][C:13]2[C:8]1=[CH:9][CH:10]=[C:11]([O:25][CH3:26])[CH:12]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]参加物
8
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of 2.39 g (6.43 mmol) of 10-hexyl-3,7-dimethoxy-phenothiazine-4-carbaldehyde in 30 ml of tetrahydrofuran was reduced with 7.0 ml of lithium borohydride solution (1M in tetrahydrofuran) analogously to that described in Example 4.1.1.da. The resulting 10-hexyl-3,7-dimethoxy-phenothiazine-4-methanol was reacted with 4.0 ml of n-butyllithium solution (1.6M in hexane) and 1.0 g (8.0 mmol) of 2-methoxyethoxymethyl chloride analogously to that described in Example 4.1.1.db. After chromatography on silica gel with diethyl ether/hexane (3:2) 2.33 g (78.5%) of 10-hexyl-3,7-dimethoxy-4-(2-methoxy-ethoxymethoxymethyl)-phenothiazine were obtained as a light yellowish oil.
出典と根拠
- ORDレコード
- ord-4ab05ff76a83408b9d85b88fb5bac813
- 出典データセット
- uspto-grants-1998_09
- 特許番号
- US05811548
反応ノート
読み込み中…