Ethyl N-(2,3-dichloro-6-nitrobenzyl)glycine → ethyl-N-(6-amino-2,3-dichlorobenzyl)glycine

HRID 481137

反応式

HRID 481137 の反応式
[CH2:1]([N:3]([CH2:8][C:9]1[C:14]([N+:15]([O-])=O)=[CH:13][CH:12]=[C:11]([Cl:18])[C:10]=1[Cl:19])[CH2:4][C:5]([OH:7])=[O:6])[CH3:2]>[Pt]>[CH2:1]([N:3]([CH2:8][C:9]1[C:14]([NH2:15])=[CH:13][CH:12]=[C:11]([Cl:18])[C:10]=1[Cl:19])[CH2:4][C:5]([OH:7])=[O:6])[CH3:2]

参加物

3

反応物 1

HCID 22439334Ethyl N-(2,3-dichloro-6-nitrobenzyl)glycine2 回

生成物 1

HCID 67080112ethyl-N-(6-amino-2,3-dichlorobenzyl)glycine

試薬・触媒・溶媒 1

HCID 23939Platinum触媒

実験手順

Ethyl N-(2,3-dichloro-6-nitrobenzyl)glycine (compound VI) may also be catalytically hydrogenated using a sulfided platinum on carbon catalyst under hydrogen pressure. The catalyst is then removed by filtration and the filtrate concentrated, diluted with water and an organic solvent and basified using an alkali to a pH of about 9-10. The organic phase is separated and concentrated and the crude material purified by low temperature recrystallization to give ethyl-(6-amino-2,3-dichlorobenzyl)glycine (compound I). 6,7-dichloro-1,5-dihydroimidazo[2,1-b]quinazoline-2(3H)one (compound III) may be prepared from compound II by suspending 5,6-dichloro-3,4-dihydro-2(1H)iminoquinazoline-3-acetate HBR (compound II) in water and adding an organic base such as TEA. After filtering the solution the filtered cake is washed in water and the solids suspended in alcohol. After filtering, the solids are rinsed in an alcohol and dried to give compound III.

後処理

  1. customThe catalyst is then removed by filtration
  2. concentrationthe filtrate concentrated
  3. additiondiluted with water
  4. customThe organic phase is separated
  5. concentrationconcentrated
  6. customthe crude material purified by low temperature recrystallization

出典と根拠

ORDレコード
ord-13078e11f0c1437fae99de3ec5765b6e
出典データセット
uspto-grants-2003_11
特許番号
US06653500B2

関連ノート

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