Methyl 3-bromobenzoate → 3-(5-Bromo-2-pyridyl)-3-pentanol
反応式
CO[C:3](=O)[C:4]1C=CC=C(Br)C=1.[C:12](OC1C=CC(Br)=CC=1C)(=O)[CH3:13].C([C:26]1[C:27]([C:33]([OH:35])=O)=[N:28][CH:29]=[C:30]([Br:32])[CH:31]=1)C.C([Mg]Br)C>C(Cl)Cl>[Br:32][C:30]1[CH:31]=[CH:26][C:27]([C:33]([OH:35])([CH2:12][CH3:13])[CH2:3][CH3:4])=[N:28][CH:29]=1参加物
6
実験手順
The title compounds were prepared using methyl-3-bromobenzoate, methyl-4-bromophenyl acetate, ethyl-5-bromo-2-carboxypyridine or ethyl-5-bromo-2-carboxypyridine and ethyl magnesium bromide with methylene chloride as solvent, respectively, but otherwise followed the procedure detailed for Preparation 36.
後処理
- customdetailed for Preparation 36
出典と根拠
- ORDレコード
- ord-af4c73c20ef94e7181eed01fd20518e4
- 出典データセット
- uspto-grants-2009_01
- 特許番号
- US07479559B2
反応ノート
読み込み中…