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Chemical Structure| 1312535-18-4 Chemical Structure| 1312535-18-4

Structure of 1312535-18-4

Chemical Structure| 1312535-18-4

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Product Details of [ 1312535-18-4 ]

CAS No. :1312535-18-4
Formula : C13H20BNO2
M.W : 233.11
SMILES Code : NC1=CC(B2OC(C)(C)C(C)(C)O2)=CC(C)=C1
MDL No. :MFCD22207064

Safety of [ 1312535-18-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1312535-18-4 ]

* 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 [ 1312535-18-4 ]

[ 1312535-18-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1312535-18-4 ]
  • [ 37554-70-4 ]
  • [ 1312535-38-8 ]
YieldReaction ConditionsOperation in experiment
With methanesulfonic acid; In 1,4-dioxane; at 100℃; INTERMEDIATE 9: 5-fluoro-4-methoxy-N-[3-methyl-5-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)phenyl]pyrimidin-2-amineTo a flask containing <strong>[37554-70-4]2-chloro-5-fluoro-4-methoxypyrimidine</strong> (0.32 g, 1.97 mmol) and 3-methyl- 5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)aniline (0.40 g, 1.72 mmol) were added dioxane (17 mL) and methanesulfonic acid (0.13 mL, 1.97 mmol). The reaction was heated at 100C overnight. The reaction was then cooled to room temperature, diluted with ethyl acetate, washed with water, dried over magnesium sulfate, filtered and concentrated. Flash chromatography was used for purification to yield 5-fluoro-4-methoxy-N-[3-methyl-5-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)phenyl]pyrimidin-2-amine. MS ESI calc'd for Ci8H2 BFN303 [M + H]+ 360, found 360. H NMR (500 MHz, DMSO-d6) delta 9.51 (s, 1H), 8.27 (d, J= 3.2, 1H), 8.00 (s, 1H),7.57 (s, 1H), 7.07 (s, 1H), 4.01 (s, 3H), 2.25 (s, 3H), 1.26 (s, 12H).
With methanesulfonic acid; In 1,4-dioxane; at 100℃; Preparative Example 1.3 - 5-Fluoro-4-methoxy-N-[3-methyl-5-(4,4,5,5-tetramethyl- 1,3,2- dioxaborolan-2-yl)phenyl]pyrimidin-2-amine PrepEx. 1.3 [00217] A solution of <strong>[37554-70-4]2-chloro-5-fluoro-4-methoxypyrimidine</strong> (0.32 g, 1.97 mmol) and 3- methyl-5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)aniline (0.40 g, 1.72 mmol) in dioxane (17 mL) and methanesulfonic acid (0.13 mL, 1.97 mmol) was heated to 100C overnight. The reaction was then cooled to room temperature, diluted with ethyl acetate, washed with water, dried over magnesium sulfate, filtered and concentrated in reduced pressure. The residue was purified by chromatography on silica gel to afford 5-fluoro-4-methoxy-N-[3-methyl-5-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl]pyrimidin-2-amine. MS ESI calc'd for Ci8H24BFN303 [M + H]+ 360, found 360. 'H NMR (500 MHz, DMSO-d6) delta 9.51 (s, 1H), 8.27 (d, J= 3.2, 1H), 8.00 (s, 1H), 7.57 (s, 1H), 7.07 (s, 1H), 4.01 (s, 3H), 2.25 (s, 3H), 1.26 (s, 12H).
With methanesulfonic acid; In 1,4-dioxane; at 100℃; Preparative Example 1.11 5-Fluoro-4-methoxy-N-[3-methyl-5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)phenyl]pyrimidin-2-amine Methanesulfonic acid (0.13 mL, 1.97 mmol) was added to a solution of 2-chloro- 5-fluoro-4-methoxypyrimidine (0.32 g, 1.97 mmol) and 3-methyl-5-(4,4,5,5-tetramethyl-l,3,2- dioxaborolan-2-yl)aniline (0.40 g, 1.72 mmol) in dioxane (17 mL). The reaction mixture was heated at 100C overnight. The reaction was then cooled to room temperature, diluted with EtOAc, washed with water, dried over magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel to afford 5- fluoro-4-methoxy-N-[3-methyl-5-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl]- pyrimidin-2-amine. MS ESI calc'd for CisH^BF sOs [M + H]+ 360, found 360. lH NMR (500 MHz, DMSO-d6) delta 9.51 (s, IH), 8.27 (d, J= 3.2, IH), 8.00 (s, IH), 7.57 (s, IH), 7.07 (s, IH), 4.01 (s, 3H), 2.25 (s, 3H), 1.26 (s, 12H).
 

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