Cyanogen Bromide → 6-Chloro-8-methyl-[1,2,4]triazolo[4,3-b]pyridazin-3-ylamine hydrobromide

HRID 532342

반응식

HRID 532342 반응식
[Cl:1][C:2]1[N:7]=[N:6][C:5]([NH:8][NH2:9])=[C:4]([CH3:10])[CH:3]=1.[N:11]#[C:12][Br:13]>CCO.O>[BrH:13].[Cl:1][C:2]1[CH:3]=[C:4]([CH3:10])[C:5]2[N:6]([C:12]([NH2:11])=[N:9][N:8]=2)[N:7]=1

참가 물질

5

실험 절차

(6-Chloro-4-methylpyridazin-3-yl)hydrazine (W3.002; 4.6 g) were initially charged in EtOH (330 ml) and water (70 ml) while stirring at RT. Thereafter, cyanogen bromide in a mixture of EtOH (170 ml) and water (30 ml) was slowly added dropwise at RT. After stirring at RT for 6 h, the mixture was left to stand overnight. Then the mixture was dried and the residue was purified using silica gel (40 g cartridge, DCM/methanol gradient of 0-10% in 30 min). 7.3 g of the title compound were obtained.

후처리

  1. additionwas slowly added dropwise at RT
  2. waitthe mixture was left
  3. waitto stand overnight
  4. customThen the mixture was dried
  5. customthe residue was purified
  6. customsilica gel (40 g cartridge, DCM/methanol gradient of 0-10% in 30 min)

출처 및 근거

ORD 기록
ord-2fda1a8a262a4bd9ac478f25b5b71584
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08853206B2

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