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Chemical Structure| 1255939-58-2 Chemical Structure| 1255939-58-2

Structure of 1255939-58-2

Chemical Structure| 1255939-58-2

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Product Details of [ 1255939-58-2 ]

CAS No. :1255939-58-2
Formula : C7H5BrClN3
M.W : 246.49
SMILES Code : CN1C=C(Br)C2=NC=NC(Cl)=C21
MDL No. :MFCD23106433

Safety of [ 1255939-58-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Application In Synthesis of [ 1255939-58-2 ]

* 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 [ 1255939-58-2 ]

[ 1255939-58-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1032650-41-1 ]
  • [ 74-88-4 ]
  • [ 1255939-58-2 ]
YieldReaction ConditionsOperation in experiment
With sodium hydride; In tetrahydrofuran; oil; for 18h; Step 1 : To Compound 13-1 (0.30g, 1.3mmol) and CH3I (0.12mL, 1.9mmol ) in THF (5mL) was added NaH (60% in oil, 0.078g, 1 ,9mmol). The mixture was stirred 18h and concentrated.
romo-4-chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine To <strong>[1032650-41-1]7-bromo-4-chloro-5H-pyrrolo[3,2-d]pyrimidine</strong> (147 mg), N,N- dimethylformamide (10 mL) was added, and NaH (36 mg) was further added thereto, followed by stirring for 30 min. Subsequently, methyl iodide was added thereto, and the reaction mixture was heated to 50C and stirred for 2 hours. After completion of the reaction, the reaction mixture was mixed with ethyl acetate and washed with water. The washed mixture was dried over anhydrous sodium sulfate, and filtered and distilled under reduced pressure to obtain the title compound. 'H NMR (300 MHz, DMSO- 6): delta 8.68(s, 1H), 8.22(s, 1H), 4.11(s, 3H).
To <strong>[1032650-41-1]7-bromo-4-chloro-5H-pyrrolo[3,2-d]pyrimidine</strong> (147 mg), N,N-dimethylformamide (10 mL) was added, and NaH (36 mg) was further added thereto, followed by stirring for 30 min. Subsequently, methyl iodide was added thereto, and the reaction mixture was heated to 50 C. and stirred for 2 hours. After completion of the reaction, the reaction mixture was mixed with ethyl acetate and washed with water. The washed mixture was dried over anhydrous sodium sulfate, and filtered and distilled under reduced pressure to obtain the title compound. [0214] 1H NMR (300 MHz, DMSO-d6): delta 8.68 (s, 1H), 8.22 (s, 1H), 4.11 (s, 3H).
Step 4: Preparation of 7-bromo-4-chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine N,N-dimethylformamide (10 mL) and NaH (36 mg) were added to <strong>[1032650-41-1]7-bromo-4-chloro-5H-pyrrolo[3,2-d]pyrimidine</strong> (147 mg), followed by stirring for 30 mins. Subsequently, methyl iodide was added thereto, and the mixture was heated under stirring at 50C for 2 hrs. Upon completion of the reaction, ethyl acetate was added thereto, and the mixture was washed with water. The resulting compound was dried over anhydrous sodium sulfate, filtered and distilled under reduced pressure to obtain the title compound. 1H NMR (300 MHz, DMSO-d6): delta 8.68(s, 1H), 8.22(s, 1H), 4.11 (s, 3H).
Step 4: Preparation of 7-bromo-4-chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine N,N-dimethylformamide (10 mL) and NaH (36 mg) were added to <strong>[1032650-41-1]7-bromo-4-chloro-5H-pyrrolo[3,2-d]pyrimidine</strong> (147 mg), followed by stirring for 30 mins. Subsequently, methyl iodide was added thereto, and the mixture was heated under stirring at 50 C. for 2 hrs. Upon completion of the reaction, ethyl acetate was added thereto, and the mixture was washed with water. The resulting compound was dried over anhydrous sodium sulfate, filtered and distilled under reduced pressure to obtain the title compound. 1H NMR (300 MHz, DMSO-d6): delta 8.68 (s, 1H), 8.22 (s, 1H), 4.11 (s, 3H).

 

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