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Chemical Structure| 89203-22-5 Chemical Structure| 89203-22-5
Chemical Structure| 89203-22-5

3-Aminopyridazine hydrochloride

CAS No.: 89203-22-5

4.5 *For Research Use Only !

Cat. No.: A194831 Purity: 98%

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Product Details of [ 89203-22-5 ]

CAS No. :89203-22-5
Formula : C4H6ClN3
M.W : 131.56
SMILES Code : [H+].C1=CC=NN=C1N.[Cl-]
MDL No. :MFCD07368609
InChI Key :GCRUEXFJNQVIJM-UHFFFAOYSA-N
Pubchem ID :16427157

Safety of [ 89203-22-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 89203-22-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 89203-22-5 ]

[ 89203-22-5 ] Synthesis Path-Downstream   1~4

  • 1
  • α-bromo-4-methoxy-2-methylsulphonamido-acetophenone [ No CAS ]
  • [ 89203-22-5 ]
  • [ 104691-56-7 ]
YieldReaction ConditionsOperation in experiment
10% EXAMPLE 19 2-(4Methoxy-2-methylsulphonamido-phenyl)-imidazo[1,2-b]pyridazine Prepared from <strong>[89203-22-5]3-amino-pyridazine-hydrochloride</strong> and alpha-bromo-4-methoxy-2-methylsulphonamido-acetophenone analogously to Example 1. Yield: 10% of theory, M.p.: 198-200 C. Calculated: C 52.81 H 4.43 N 17.60 S 10.07: Found: 53.08 4.28 17.69 10.73.
  • 2
  • [ 104462-28-4 ]
  • [ 89203-22-5 ]
  • [ 104691-57-8 ]
YieldReaction ConditionsOperation in experiment
7% EXAMPLE 20 2-(2-Methoxy-4-methylsulphonyloxy-phenyl)-imidazo[1,2-b]pyridazine Prepared from <strong>[89203-22-5]3-amino-pyridazine-hydrochloride</strong> and alpha-bromo-2-methoxy-4-methylsulphonyloxy-acetophenone analogously to Example 1. Yield: 7% of theory, M.p.: 150-151 C. Calculated: C 52.65 H 4.10 N 13.16 S 10.04: Found: 52.88 4.29 13.28 9.94.
  • 3
  • [ 24424-99-5 ]
  • [ 89203-22-5 ]
  • [ 147362-90-1 ]
YieldReaction ConditionsOperation in experiment
1,1-Dimethylethyl 3-pyridazinylcarbamate To a stirred suspension of <strong>[89203-22-5]3-pyridazinamine hydrochloride</strong> (100 g, 760 mmol) in DCM (1000 ml) TEA (212 ml, 1520 mmol) was added dropwise under argon flow. The mixture was stirred for 10 minutes then DMAP (13.93 g, 114 mmol) was added portion-wise and the resulting mixture was stirred for 5 minutes then Boc2O (194 ml, 836 mmol) was added and the mixture was stirred at room temperature overnight. Water (1000 ml) and DCM (500 ml) were added, phases were separated and the organic phase was washed with H2O/saturated NH4Cl solution (1/1) (2*1.5 l).The organic phase was filtered, washed with H2O (500 ml) and dried over Na2SO4. Solvent was removed and the resulting crude was purified by flash chromatography eluding with 100% EtOAc to afford the title compound (113 g). 1H NMR (400 MHz, CDCl3): delta 8.88 (dd, 1H), 8.24 (d, 1H), 7.79 (br s, 1H), 7.44 (dd, 1H), 1.55 (s, 9H).
  • 4
  • [ 1431654-29-3 ]
  • [ 89203-22-5 ]
  • [ 1431647-05-0 ]
YieldReaction ConditionsOperation in experiment
11% With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 60.0℃; for 3.5h;Inert atmosphere; 2,8-dimethyl-6-(2-(trifluoromethyl)phenyl)imidazo[1,2-b]pyridazine-3-carboxylic acid (150.0 mg, 0.45 mmol) was dissolved in DMF (2.4 mL). HATU (255.0 mg, 0.67 mmol) was added, followed by diisopropylethylamine (0.312 mL, 1.79 mmol). 3-aminopyridazine-HCl (59.0 mg, 0.45 mmol) was slurried in DMF (2.4 mL) and diisopropylethylamine (0.078 mL, 0.45 mmol) and added to the reaction mixture. This was warmed to 60 C and allowed to stir under nitrogen atmosphere for 3.5 h. The mixture was cooled to room temp, and saturated aqueous NaHCO3 was added (6 mL), then water was added (10 mL). This was extracted with EtOAc (3x20 mL) and the combined organics were washed with brine, dried with anhydrous Na2SO4, filtered, and concentrated. The crude product was purified by silica gel column chromatography using a gradient of 0 - 10% MeOH in CH2Cl2 to give 2,8-dimethyl-N-(pyridazin-3-yl)-6-(2-(trifluoromethyl)phenyl)imidazo[1,2-b]pyridazine-3-carboxamide (19.6 mg, 11%). MS (ESI) calcd for C20H15F3N6O: 412.13; found: 413.2 [M+H]
11% With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 60.0℃; for 3.5h;Inert atmosphere; 2,8-dimethyl-6-(2-(trifluoromethyl)phenyl)imidazo[1,2-b]pyridazine-3-carboxylic acid (150.0 mg, 0.45 mmol) was dissolved in DMF (2.4 mL). HATU (255.0 mg, 0.67 mmol) was added, followed by diisopropylethylamine (0.312 mL, 1.79 mmol). 3-aminopyridazine-HCl (59.0 mg, 0.45 mmol) was slurried in DMF (2.4 mL) and diisopropylethylamine (0.078 mL, 0.45 mmol) and added to the reaction mixture. This was warmed to 60 C and allowed to stir under nitrogen atmosphere for 3.5 h. The mixture was cooled to room temp, and saturated aqueous NaHCO3 was added (6 mL), then water was added (10 mL). This was extracted with EtOAc (3x20 mL) and the combined organics were washed with brine, dried with anhydrous Na2SO4, filtered, and concentrated. The crude product was purified by silica gel column chromatography using a gradient of 0 - 10% MeOH in CH2Cl2 to give 2,8-dimethyl-N-(pyridazin-3-yl)-6-(2-(trifluoromethyl)phenyl) imidazo[1,2-b]pyridazine-3-carboxamide (19.6 mg, 11%). MS (ESI) calcd for C20H15F3N6O: 412.13; found: 413.2 [M+H].
 

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