Tetrahydrofuran → N-methanesulfonyl-N1-[4-(4-ethyl-2-hydroxyphenoxy)-3-fluorophenyl]propan-1,3-diamine
反応式
[CH3:1][S:2]([N:5]([C:10]1[CH:15]=[CH:14][C:13]([O:16][C:17]2[CH:22]=[CH:21][C:20]([CH2:23][CH3:24])=[CH:19][C:18]=2[O:25]CC2C=CC=CC=2)=[C:12]([F:33])[CH:11]=1)[CH2:6][CH2:7][CH2:8][NH2:9])(=[O:4])=[O:3].O1CCCC1>CO>[CH3:1][S:2]([N:5]([C:10]1[CH:15]=[CH:14][C:13]([O:16][C:17]2[CH:22]=[CH:21][C:20]([CH2:23][CH3:24])=[CH:19][C:18]=2[OH:25])=[C:12]([F:33])[CH:11]=1)[CH2:6][CH2:7][CH2:8][NH2:9])(=[O:3])=[O:4]参加物
4
実験手順
According to the procedure of example 20 (b) except substituting 4-ethyl-2-methoxy-1-[4-nitro-2-(trifluoromethyl) phenoxy]benzene for N-Methanesulfonyl-N1-[4-(2-benzyloxy-4-ethylphenoxy)-3-fluorophenyl]propan-1,3-diamine (90 mg, 0.19 mmol) and tetrahydrofurane for methanol (15 mL), the title compound (50 mg, 68%) was obtained as a brown liquid, after purification on silica gel (dichloromethane/ethyl acetate: 8/2)
出典と根拠
- ORDレコード
- ord-bebafff9c0ce427f81c854ce35988f46
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09309179B2
反応ノート
読み込み中…