Ethanethiol → 4-Bromo-3-(ethylthio)-N-methyl-2-nitroaniline
反応式
[Br:1][C:2]1[CH:9]=[CH:8][C:5]([NH:6][CH3:7])=[C:4]([N+:10]([O-:12])=[O:11])[C:3]=1F.[CH2:14]([SH:16])[CH3:15]>>[Br:1][C:2]1[CH:9]=[CH:8][C:5]([NH:6][CH3:7])=[C:4]([N+:10]([O-:12])=[O:11])[C:3]=1[S:16][CH2:14][CH3:15]参加物
3
実験手順
This compound was synthesized according to the procedure of Example 11, Step 1, using 4-bromo-3-fluoro-N-methyl-2-nitroaniline and ethanethiol as the starting materials. LCMS calculated for C9H12BrN2O2S (M+H)+: m/z=291.0, 293.0. found: 290.9, 292.9.
後処理
- customThis compound was synthesized
出典と根拠
- ORDレコード
- ord-bb6929217e8640c397b1b8c55ef1db52
- 出典データセット
- uspto-grants-2016_07
- 特許番号
- US09399640B2
反応ノート
読み込み中…