Chloroacetyl chloride → 5-Bromo-N'-(chloroacetyl)-3-pyridinecarbohydrazide

HRID 2101835ノート

反応式

HRID 2101835 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([C:8]([NH:10][NH2:11])=[O:9])[CH:5]=[N:6][CH:7]=1.CN1CCOCC1.[Cl:19][CH2:20][C:21](Cl)=[O:22]>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([C:8]([NH:10][NH:11][C:21](=[O:22])[CH2:20][Cl:19])=[O:9])[CH:5]=[N:6][CH:7]=1

参加物

5

反応物 3

HCID 6577Chloroacetyl chlorideHCID 79724-MethylmorpholineHCID 6963655-Bromonicotinohydrazide

生成物 1

HCID 578003225-Bromo-N'-(chloroacetyl)-3-pyridinecarbohydrazide収率 90.1%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To an ice-cold suspension of 5-bromo-3-pyridinecarbohydrazide (3.0 g, 13.88 mmol) in anhydrous CH2Cl2 (60 mL) was added 4-methyl-morpholine (2.1 g, 20.82 mmol), followed by dropwise addition of chloroacetyl chloride (1.88 g, 16.67 mmol). The cold bath was then removed and the mixture stirred at rt for 15 h. Heavy precipitation occurred and the mixture was diluted with additional CH2Cl2 (50 mL) and stirring continued for 24 h. The solids were collected by filtration and washed with CH2Cl2 to afford the title compound (3.66 g, 90% yield): MS (ES) m/z 292 and 294 (M+1 Br isotopes).

後処理

  1. customThe cold bath was then removed
  2. customHeavy precipitation
  3. additionthe mixture was diluted with additional CH2Cl2 (50 mL)
  4. stirringstirring
  5. waitcontinued for 24 h
  6. filtrationThe solids were collected by filtration
  7. washwashed with CH2Cl2

出典と根拠

ORDレコード
ord-6b41a0690ec24b2993bc0c677d5631f6
出典データセット
uspto-grants-2009_08
特許番号
US07572820B2

反応ノート

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