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Chemical Structure| 389606-35-3 Chemical Structure| 389606-35-3

Structure of 389606-35-3

Chemical Structure| 389606-35-3

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Product Details of [ 389606-35-3 ]

CAS No. :389606-35-3
Formula : C9H11Cl2N3O
M.W : 248.11
SMILES Code : O=C(C1=CN=C(Cl)N=C1Cl)NC(C)(C)C
MDL No. :MFCD27952605

Safety of [ 389606-35-3 ]

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

Application In Synthesis of [ 389606-35-3 ]

* 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 [ 389606-35-3 ]

[ 389606-35-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 75-64-9 ]
  • [ 2972-52-3 ]
  • [ 389606-35-3 ]
YieldReaction ConditionsOperation in experiment
90% With triethylamine; In tetrahydrofuran; Method 79 5-N-t-Butylcarbamoyl-2,4-dichloropyrimidine. A solution of 2,4-dichloro-5-chloroformylpyrimidine (Method 31; 9.8 g, 46.3 mmol) in dry THF (50 ml) was cooled to -15 C. t-Butylamine (5.2 ml, 49.3 mmol) and triethylamine (6.9 ml, 49.5 mmol) in dry THF (20 ml) were added slowly so as to maintain the temperature below -10 C. The resulting mixture was stirred at -10 C. for 2 hours, allowed to warm to ambient temperature and stirred for a further 30 minutes. The precipitate was removed by filtration and the filtrate evaporated to give a viscous oil, and then evaporated under high vacuum to give the title compound as a solid (10.48 g, 90%). NMR: 1.49 (s, 9H), 6.19 (brs, 1H), 8.86 (s, 1H); m/z: 248.
85% With triethylamine; In chloroform; at 0℃; for 1h; 100 g of 2,4-dichloro-5-pyrimidinyl chloride is dissolved in 800 g of anhydrous chloroform,Add 95 grams of triethylamine, lower the temperature to 0 C, and add 38 grams of tert-butylamine dropwise.After the addition, the reaction was held at 0 C for 1 hour.100 g of compound 2,4-dichloro-5-pyrimidine tert-butyramide was obtained by filtration,The measured purity is greater than 98% and the yield is 85%;
50% With triethylamine; In tetrahydrofuran; at -15 - 20℃; for 3h; 4b Production of 2,4-Dichloro-pyrimidine-5-carboxylic acid-tert-butylamide A solution of 24.85 g (117.5 mmol) of 2,4-dichloro-pyrimidine-5-carbonyl chloride in 125 ml of THF is cooled to -15 C. It is slowly mixed with a solution of 13.2 ml (124.5 mmol) of tert-buylamine and 17.4 ml (125.7 mmol) of triethylamine in 50 ml of THF, so that the temperature of the reaction mixture remains less than -10 C. It is stirred for another 2 hours at -10 C., then the cooling bath is removed, and the reaction mixture is heated to room temperature while being stirred. After 1 hour, the precipitate that is formed is filtered off, and the filtrate is completely concentrated by evaporation. The residue that is obtained is purified by chromatography (hexane/ethyl acetate 4:1). 14.01 g (56.6 mmol, corresponding to 50% of theory) of the product is obtained. 1H-NMR (DMSO): 8.81 (s, 1H), 8.34 (s, 1H), 1.36 (s, 9H)
With triethylamine; In tetrahydrofuran; at -7 - 20℃; for 4h; Preparation of 2,4-dichloro-pyhmidine-5- tert-butylcarboxamide (Vl):; A solution of 13,7 ml (129 mmol) terf.-butylamine and 17,9 ml (129 mmol) triethylamine in 163 ml THF is added dropwise under argon over a period of 70 minutes to a solution of 26,0 g (123 mmol) 2,4-dichloro-pyrimidine-5- carbonyl chloride at -7C to -3C. The mixture is kept at this temperature for 4 hours and then slowly warmed to room temperature. The precipitate that forms is filtered off and the filtrate concentrated to dryness. 32,6 g of the product, which is used without further purification, is obtained. 1H-NMR (DMSO): 8.79 (s, 1 H), 8.29 (s, 1 H), 1.32 (s, 9H).
With triethylamine; In tetrahydrofuran; at -7 - -3℃; for 5.16667h; A solution of 13,7 ml (129 mmol) tert.-butylamine and 17,9 ml (129 mmol) triethylamine in 163 ml THF is added dropwise under argon over a period of 70 minutes to a solution of 26,0 g (123 mmol) 2,4-dichloro-pyrimidine-5-carbonyl chloride at -7 C. to -3 C. The mixture is kept at this temperature for 4 hours and then slowly warmed to room temperature. The precipitate that forms is filtered off and the filtrate concentrated to dryness. 32,6 g of the product, which is used without further purification, is obtained. 1H-NMR (DMSO): 8.79 (s, 1H), 8.29 (s, 1H), 1.32 (s, 9H).

 

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