反応式
[NH2:1][C:2]1[C:3]([C:9]([O:11]C)=[O:10])=[N:4][C:5]([Br:8])=[CH:6][CH:7]=1.[Li+].[OH-].Cl>C1COCC1.CO>[NH2:1][C:2]1[C:3]([C:9]([OH:11])=[O:10])=[N:4][C:5]([Br:8])=[CH:6][CH:7]=1参加物
5
実験手順
To a solution of methyl 3-amino-6-bromopicolinate (2.31 g, 10 mmoles) in 2:1 THF/MeOH (51 mL) was added 1.0 M LiOH (17 mL, 17 mmoles). After stirring for 16 hours, 1 N HCl (17 mL, 17 mmoles) was added and the THF/MeOH was removed in vacuo. The resulting solid was filtered, rinsed with cold H2O (4×20 mL) and pumped on yielding 3-amino-6-bromopicolinic acid (97%). LCMS (m/z): 216.9 (MH+); LC Rt=1.93 min.
後処理
- customthe THF/MeOH was removed in vacuo
- filtrationThe resulting solid was filtered
- washrinsed with cold H2O (4×20 mL)
出典と根拠
- ORDレコード
- ord-d0e2ccb450fe471bbb99ddb873041bc0
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08822497B2
関連ノート
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