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Chemical Structure| 2580098-92-4 Chemical Structure| 2580098-92-4

Structure of 2580098-92-4

Chemical Structure| 2580098-92-4

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Product Details of [ 2580098-92-4 ]

CAS No. :2580098-92-4
Formula : C6H13Cl2N3
M.W : 198.09
SMILES Code : C[C@H](N)C1=CN(C)N=C1.[H]Cl.[H]Cl
English Name :(S)-1-(1-Methyl-1H-pyrazol-4-yl)ethan-1-amine dihydrochloride

Safety of [ 2580098-92-4 ]

Application In Synthesis of [ 2580098-92-4 ]

* 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 [ 2580098-92-4 ]

[ 2580098-92-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 2839856-24-3 ]
  • [ 2580098-92-4 ]
  • [ 2839855-75-1 ]
YieldReaction ConditionsOperation in experiment
76 % With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; Inert atmosphere; 14.4 Step 4: Synthesis of (S)-6-(4-chlorophenyl)-N-(1-(1-methyl-1H-pyrazol-4-yl)ethyl)-2-(1-methyl-1H-pyrazol-4-yl)pyrimidine-4-carboxamide (Compound 14) 6-(4-chlorophenyl)-2-(1-methyl-1H-pyrazol-4-yl)pyrimidine-4-carboxylic acid (100mg, 0.32mmol), (S)-(1-methyl -1H-pyrazol-4-yl)ethyl-1-amine hydrochloride (67mg, 0.42mmol) was dissolved in 10ml of tetrahydrofuran, and N,N-diisopropylethylamine (108mg, 0.84mmol ) and 1-propylphosphoric anhydride (350mg, 0.55mmol), the reaction was stirred at room temperature for 2h. The crude product was separated by forward column chromatography to obtain (S)-6-(4-chlorophenyl)-N-(1-(1-methyl-1H-pyrazol-4-yl)ethyl)-2-( 1-methyl-1H-pyrazol-4-yl)pyrimidine-4-carboxamide (compound 14), white solid 102 mg, yield 76%
  • 2
  • [ 2813339-11-4 ]
  • [ 2580098-92-4 ]
YieldReaction ConditionsOperation in experiment
70 % With hydrogenchloride In tetrahydrofuran; 1,4-dioxane at 20℃; Inert atmosphere; 14.3 Step 3: Synthesis of (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl-1-amine hydrochloride (14-c) Dissolve (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl-2-sulfinamide (1.59g, 6.9mmol) in 30mL tetrahydrofuran, add 4M hydrochloric acid 1,4 - Dioxane solution (7.4mL, 29.6mmol) The reaction was stirred at room temperature for 3h. After the reaction, the solid was rinsed twice with ethyl acetate and petroleum ether, and dried to obtain (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl -1-amine hydrochloride (14-c), white solid 0.61g, yield 70%
70 % With hydrogenchloride In tetrahydrofuran; 1,4-dioxane at 20℃; 109 Synthesis of (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl-1-amine hydrochloride: (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl-2-sulfenamide (1.59g, 6.9mmol) was dissolved in 30mL tetrahydrofuran, and 4M hydrochloric acid 1,4-dioxane solution (7.4mL, 29.6mmol) was added to react and stirred at room temperature for 3h. After the reaction was completed, the solid was pulled dry, and the solid was washed twice with ethyl acetate and twice with petroleum ether. The solid was dried to obtain (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl-1-amine hydrochloride, 0.61g of white solid, and the yield was 70%
70 % With hydrogenchloride In tetrahydrofuran; 1,4-dioxane at 20℃; 109 Synthesis of (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl-1-amine hydrochloride: (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl-2-sulfenamide (1.59g, 6.9mmol) was dissolved in 30mL tetrahydrofuran, and 4M hydrochloric acid 1,4-dioxane solution (7.4mL, 29.6mmol) was added to react and stirred at room temperature for 3h. After the reaction was completed, the solid was pulled dry, and the solid was washed twice with ethyl acetate and twice with petroleum ether. The solid was dried to obtain (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl-1-amine hydrochloride, 0.61g of white solid, and the yield was 70%
  • 3
  • [ 2242467-80-5 ]
  • [ 2580098-92-4 ]
  • [ 2813337-98-1 ]
YieldReaction ConditionsOperation in experiment
55 % 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 20℃; 109 Synthesis of (S)-6-(4-chlorophenyl)-2-(1-methyl-1H-pyrazol-4-yl)-N-(1-(1-methyl-1H-pyrazol-4-yl)ethyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide: Dissolve 6-(4-chlorophenyl)-2-(1-methyl-1H-pyrazol-4-yl)-3-oxo-2,3-dihydropyridazine-4-carboxylic acid (50 mg, 0.15 mmol) and (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl-1-amine (27 mg, 0.22 mmol) in 3 mL N, N-dimethylformamide,N, N-diisopropylethylamine (39 mg, 0.30 mmol) and 2-(7-azobenzotriazole)-N, N, N', N'-tetramethyluronium hexafluorophosphate (114 mg, 0.30 mmol) were added in sequence at room temperature,and the reaction was stirred at room temperature for 8 hours. The crude product was purified by reverse column to obtain (S)-6-(4-chlorophenyl)-2-(1-methyl-1H-pyrazol-4-yl)-N-(1-(1-methyl-1H-pyrazol-4-yl)ethyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide, 36 mg of light yellow solid, yield 55%.
55 % 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 20℃; 109 Synthesis of (S)-6-(4-chlorophenyl)-2-(1-methyl-1H-pyrazol-4-yl)-N-(1-(1-methyl-1H-pyrazol-4-yl)ethyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide: Dissolve 6-(4-chlorophenyl)-2-(1-methyl-1H-pyrazol-4-yl)-3-oxo-2,3-dihydropyridazine-4-carboxylic acid (50 mg, 0.15 mmol) and (S)-1-(1-methyl-1H-pyrazol-4-yl)ethyl-1-amine (27 mg, 0.22 mmol) in 3 mL N, N-dimethylformamide,N, N-diisopropylethylamine (39 mg, 0.30 mmol) and 2-(7-azobenzotriazole)-N, N, N', N'-tetramethyluronium hexafluorophosphate (114 mg, 0.30 mmol) were added in sequence at room temperature,and the reaction was stirred at room temperature for 8 hours. The crude product was purified by reverse column to obtain (S)-6-(4-chlorophenyl)-2-(1-methyl-1H-pyrazol-4-yl)-N-(1-(1-methyl-1H-pyrazol-4-yl)ethyl)-3-oxo-2,3-dihydropyridazine-4-carboxamide, 36 mg of light yellow solid, yield 55%.
 

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