(2-Chloropyridin-3-yl)boronic acid → 2-chloro-N-methyl-3,4'-bipyridin-3'-amine
反応式
I[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[NH:8][CH3:9].[Cl:10][C:11]1[C:16](B(O)O)=[CH:15][CH:14]=[CH:13][N:12]=1>>[Cl:10][C:11]1[C:16]([C:2]2[CH:7]=[CH:6][N:5]=[CH:4][C:3]=2[NH:8][CH3:9])=[CH:15][CH:14]=[CH:13][N:12]=1参加物
3
実験手順
The title compound was prepared in analogy to example 72, from (4-iodo-pyridin-3-yl)-methyl-amine and 2-chloropyridin-3-ylboronic acid after a reaction time of 5 hours at 90° C. The compound was purified by silica gel chromatography on a 50 g column using an MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane:EtOAc (100:0 to 0:100). Light yellow solid (82%). MS (EI): m/z=219 [M]+.
後処理
- customThe compound was purified by silica gel chromatography on a 50 g column
- washeluting with a gradient of n-heptane:EtOAc (100:0 to 0:100)
出典と根拠
- ORDレコード
- ord-0eac17388f6e43f7a42aaa4aa2059dad
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08987307B2
反応ノート
読み込み中…