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Chemical Structure| 59368-16-0 Chemical Structure| 59368-16-0

Structure of 59368-16-0

Chemical Structure| 59368-16-0

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Product Details of [ 59368-16-0 ]

CAS No. :59368-16-0
Formula : C7H7BrN6
M.W : 255.07
SMILES Code : NC1=NC(N)=C2N=C(CBr)C=NC2=N1
MDL No. :MFCD13180628

Safety of [ 59368-16-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P280

Application In Synthesis of [ 59368-16-0 ]

* 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 [ 59368-16-0 ]

[ 59368-16-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 945-24-4 ]
  • [ 59368-16-0 ]
YieldReaction ConditionsOperation in experiment
With bromine; triphenylphosphine; In ISOPROPYLAMIDE; at 20℃; for 18h; To a solution of triphenylphosphene (408 mg, 1 .03 mmol) in anhydrous DMA ( 1 mL) is added bromine dropwise at 0 0C (0.08 mL, 1 .03 mmol) under N2 atmosphere. After stirring for 5 additional minutes, <strong>[945-24-4](2,4-diaminopteridin-6-yl)methanol</strong> (100 mg, 0.33 mmol) is added at once and the reaction mixture is stirred at RT for 18 h. Barium oxide ( 100 mg, 0.65 mmol) is then added to the reaction mixture followed by 3-aminobenzoic acid (107 mg, 0.78 mmol) at RT. The reaction mixture is then heated at 56 0C and stirred at that temperature for 24 h and cooled to RT. The mixture is diluted with methylene chloride (5 mL) and the resulting brownish precipitate is filtered. The solids are washed with water and methanol. The solids are then taken in methanol and heated at reflux for 2 h. After cooling to RT, the solids are filtered again and dried overnight in a heated vacuum oven to give 45 mg product (Yield: 26.9%) as a brownish yellow solid. 1 H NMR (500 MHz, DMSOd6) delta 4.6 (br s, 2H), 6.7 (s, 1 H), 6.9-7.0 (d, 1 H), 7.15-7.3 (m, 2H), 7.38 (br s, 2H), 8.6-8.7 (br s, I H), 8.9 (s, I H), 9.3-9.4 (m, 2H), 12.8 (br s, I H); LC-MS m/z 312 (MH+), retention time 1 1 .48 min., HPLC Method B.
With dibromotriphenylphosphorane; In N,N-dimethyl acetamide; The compound 13 was allowed to react with triphenylphosphine dibromide in DMA to obtain a compound 14.The compound 14 was dissolved in DMA under nitrogen gas stream, and then the compound 15 and DIEA were addedand reacted to obtain a compound 16 (yield: 69%). Subsequently, the compound 16 and the compound 17 were dissolvedin DMSO under nitrogen gas stream, and condensation reaction was performed with a BOP reagent to obtain a compound18 (yield: 46%). Subsequently, the compound 18 and the compound 19 were dissolved in DMA under nitrogen gasstream, and condensation reaction was performed with HATU to obtain a compound 20 (yield: 69%). Then, the compound20 was dissolved in dichloromethane, and deprotection was performed with TFA to obtain a compound 21 (MTX-NH2).
  • 2
  • [ 59368-16-0 ]
  • [ 174579-31-8 ]
  • [ 1246636-77-0 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; acetonitrile; at 70℃; for 15h; Crude 6-(bromomethyl)-2,4-pteridinediamine (Step 1 , Example 19)(80 mg, 0.392 mmol), <strong>[174579-31-8]tert-butyl 2-(4-aminophenyl)acetate</strong> (228 mg, 1.12 mmol), and K2CO3 (542 mg, 3.9 mmol) are dissolved in a DMF (1 mL), CH3CN (3 mL) mixture and heated to 70 0C overnight (15 h). The crude reaction mixture is filtered and washed with MeOH ( 30 mL). The filtrate is concentrated by rotoevaporation, dissolved in minimum amount of MeOH (5 mL), and filtered again by syringe filter (0.45 um) for purification by prep HPLC using Method 1. The desired fractions are combined and concentrated to give 15 mg of tert-butyl 2-(4- ((2,4-diaminopteridin-6-yl)methylamino) phenyl)acetate (Yield; 10%).
 

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