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Ammonium Hydroxide → 3,6-Dichloropyridazine-4-carboxamide

HRID 869163
ノート
印刷プレビュー

反応式

HRID 869163 の反応式
[NH4+].[OH-].C([N:6](C(C)C)CC)(C)C.[Cl:12][C:13]1[N:14]=[N:15][C:16]([Cl:22])=[CH:17][C:18]=1[C:19](Cl)=[O:20]>C1COCC1.CN(C1C=CN=CC=1)C>[Cl:12][C:13]1[N:14]=[N:15][C:16]([Cl:22])=[CH:17][C:18]=1[C:19]([NH2:6])=[O:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 14923Ammonium HydroxideHCID 810183,6-Dichloropyridazine-4-carbonyl chlorideHCID 81531Diisopropylethylamine

生成物 1

HCID 2620493,6-Dichloropyridazine-4-carboxamide収率 96.7%

試薬・触媒・溶媒 2

HCID 142844-(Dimethylamino)pyridine触媒HCID 8028Tetrahydrofuran
このページの内容参加物実験手順後処理出典と根拠反応ノート
溶媒

実験手順

A solution of NH4OH (1.1 mL, 17 mmol, 1.2 equiv) and diisopropylethylamine (6.2 mL, 36 mmol, 2.1 equiv) in THF (57 mL) was sonicated until homogeneous after which was added DMAP (1.0 g, 14 mmol, 1.0 equiv). 3,6-dichloropyridazine-4-carbonyl chloride (3.0 g, 14 mmol, 1.0 equiv) was then added and the solution was stirred at room temperature for 20 minutes. The solution was filtered and partitioned between EtOAc and 1M KHSO4 solution. The organic layer was washed once more with 1M KHSO4 and saturated NaCl, dried over Na2SO4, and evaporated to dryness to give the desired product (2.6 g, 96%).

後処理

  1. filtrationThe solution was filtered
  2. custompartitioned between EtOAc and 1M KHSO4 solution
  3. washThe organic layer was washed once more with 1M KHSO4 and saturated NaCl
  4. dry with materialdried over Na2SO4
  5. customevaporated to dryness

出典と根拠

ORDレコード
ord-d019315dba9342ab9d51e5345a0fc0a8
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08969346B2

反応ノート

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