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Chemical Structure| 1416366-34-1 Chemical Structure| 1416366-34-1

Structure of 1416366-34-1

Chemical Structure| 1416366-34-1

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Product Details of [ 1416366-34-1 ]

CAS No. :1416366-34-1
Formula : C6H7ClN2O
M.W : 158.59
SMILES Code : COCC1=CN=C(Cl)N=C1
MDL No. :MFCD28385449

Safety of [ 1416366-34-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H320-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1416366-34-1 ]

* 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 [ 1416366-34-1 ]

[ 1416366-34-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1046816-75-4 ]
  • [ 74-88-4 ]
  • [ 1416366-34-1 ]
YieldReaction ConditionsOperation in experiment
66% With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20℃; for 0.833333h; To a solution of <strong>[1046816-75-4]2-chloro-5-hydroxymethyl-pyrimidine</strong> (9.0 g, 62 mmol) in 70 ml of anhydrous DMF was added methyl iodide (6 eq. 370 mmol, 23 ml). The mixture was cooled to 0°C, then NaH (2.6 lg, 1.05 eq.) was added in portions over 5 mins. The resulting mixture was stirred 25 min. at 0°C, then 25 min. at rt. The reaction mixture was then cooled in ice bath, and quenched by addition of saturated NH4C1 aq. solution (200 ml ), extracted with ether (150 ml x 3). The combined organic layers were washed by brine, dried over Na2S04, filtered and concentrated in vacuo. The residue was purified by ISCO column (330 g of silica gel) using ethyl acetate in hexane (0-90percent ethyl acetate, 2500 ml, then 1000 ml of ethyl acetate) to give 6.5g (66percent) of the title compound: MS (ESI) mlz 159.2 (M+H); 1H NMR (500 MHz, CDC13) delta 8.60 (s, 2H), 4.48 (s, 2H), 3.45 (s, 3H).
66% With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20℃; for 0.916667h; To a solution of <strong>[1046816-75-4]2-chloro-5-hydroxymethyl-pyrimidine</strong> (9.0 g, 62 mmol) in 70 ml of anhydrous DMF was added methyl iodide (6 eq. 370 mmol, 23 ml). The mixture was cooled to 0°C, then NaH (2.6 lg, 1.05 eq.) was added in portions over 5 mins. The resulting mixture was stirred 25 min. at 0°C, then 25 min. at rt. The reaction mixture was then cooled in ice bath, and quenched by addition of saturated NH4CI aq. solution (200 ml ), extracted with ether (150 ml x 3). The combined organic layers were washed by brine, dried over Na2S04, filtered and concentrated in vacuo. The residue was purified by ISCO column (330 g of silica gel) using ethyl acetate in hexane (0-90percent ethyl acetate, 2500 ml, then 1000 ml of ethyl acetate) to give 6.5g (66percent) of the title compound: MS (ESI) mlz 159.2 (M+H); NMR (500 MHz, CDC13) delta 8.60 (s, 2H), 4.48 (s, 2H), 3.45 (s, 3H).
66% With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20℃; for 0.833333h; To a solution of<strong>[1046816-75-4]2-chloro-5-hydroxymethyl-pyrimidine</strong> (9.0 g, 62 mmol) in 70 ml ofanhydrous DMF was added methyl iodide (6 eq. 370 mmol, 23 ml). The mixture was cooled to0°C, then NaH (2.61g, 1.05 eq.) was added in portions over 5 mins. The resulting mixture wasstirred 25 min. at 0°C, then 25 min. at rt. The reaction mixture was then cooled in ice bath, and10 quenched by addition of saturated NH4Cl aq. solution (200 ml ), extracted with ether (150 ml x3). The combined organic layers were washed by brine, dried over Na2S04, filtered andconcentrated in vacuo. The residue was purified by ISCO column (330 g of silica gel) usingethyl acetate in hexane (0-90percent ethyl acetate, 2500 ml, then 1000 ml of ethyl acetate) to give 6.5g(66percent) of the title compound: 1H NMR (500 MHz, CDCh) 8 8.60 (s, 2H), 4.48 (s, 2H), 3.45 (s,15 3H). MS ESI m/z 159.2 (M+H).
Preparation of 2-chloro-5-methoxymethylpyrimidine 18To a solution of <strong>[1046816-75-4]2-chloro-5-hydroxymethyl-pyrimidine</strong> (9.0 g, 62 mmol) in 70 ml of anhydrous DMF was added methyl iodide (6 eq. 370 mmol, 23 ml). The mixture was cooled to 0°C, then NaH (2.6 lg, 1.05 eq.) was added in portions over 5 mins. The resulting mixture was stirred 25 min. at 0°C, then 25 min. at rt. The reaction mixture was then cooled in ice bath, and quenched by addition of saturated NH4C1 aq. solution (200 ml ), extracted with ether (150 ml x 3). The combined organic layers were washed by brine, dried over Na2S04, filtered and concentrated in vacuo. The residue was purified by IS CO column (330 g of silica gel) using ethyl acetate in hexane (0-90percent ethyl acetate, 2500 ml, then 1000 ml of ethyl acetate) to give 6.5g (66percent) of the title compound: MS (ESI) mlz 159.2 (M+H); 1H NMR (500 MHz, CDC13) delta 8.60 (s, 2H), 4.48 (s, 2H), 3.45 (s, 3H).

 

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