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Ammonium Hydroxide → 6-Chloro-4-methylpyridazin-3-amine

HRID 1943451
ノート
印刷プレビュー

反応式

HRID 1943451 の反応式
Cl[C:2]1[N:3]=[N:4][C:5]([Cl:9])=[CH:6][C:7]=1[CH3:8].[OH-].[NH4+].ClC1N=[N:17]C(N)=CC=1C>>[Cl:9][C:5]1[N:4]=[N:3][C:2]([NH2:17])=[C:7]([CH3:8])[CH:6]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 14923Ammonium HydroxideHCID 879233,6-Dichloro-4-methylpyridazineHCID 123536636-Chloro-5-methylpyridazin-3-amine

生成物 1

HCID 123536646-Chloro-4-methylpyridazin-3-amine収率 85%

反応条件

温度
100 °C

実験手順

A 20 mL microwave vial was charged with, a stir bar, 3,6-dichloro-4-methylpyridazine (4.0 g, 24.54 mmol) and 14 mL of a new, freshly opened bottle of ammonium hydroxide. The vial was quickly sealed. The solution was heated in a microwave (Personal Chemistry, Emrys Optimizer) to 100° C. for 3 h. The vial was cooled, opened, and a stream of nitrogen was used to remove excess ammonium hydroxide. Water was added, the solid was collected by filtration, washed with water and dried to provide a mixture of 6-chloro-5-methylpyridazin-3-amine and 6-chloro-4-methylpyridazin-3-amine (3 g, 20.90 mmol, 85% yield). The mixture was used without further purification.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. additionA 20 mL microwave vial was charged with, a stir bar
  2. customThe vial was quickly sealed
  3. temperatureThe vial was cooled
  4. customto remove excess ammonium hydroxide
  5. additionWater was added
  6. filtrationthe solid was collected by filtration
  7. washwashed with water
  8. customdried
  9. customto provide

出典と根拠

ORDレコード
ord-17f349d1596a4a1d8a51fa6bcf729892
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08389527B2

反応ノート

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