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

HRID 1943451
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HRID 1943451 반응식
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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

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

생성물 1

HCID 123536646-Chloro-4-methylpyridazin-3-amine수율 85%

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온도
100 °C

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-17f349d1596a4a1d8a51fa6bcf729892
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08389527B2

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