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Chemical Structure| 76872-71-4 Chemical Structure| 76872-71-4

Structure of 76872-71-4

Chemical Structure| 76872-71-4

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Product Details of [ 76872-71-4 ]

CAS No. :76872-71-4
Formula : C7H6N2O2S
M.W : 182.20
SMILES Code : O=C1NC2=C(C=C(C)S2)C(N1)=O
MDL No. :MFCD16473216

Safety of [ 76872-71-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 76872-71-4 ]

* 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 [ 76872-71-4 ]

[ 76872-71-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 76872-71-4 ]
  • [ 76872-23-6 ]
YieldReaction ConditionsOperation in experiment
74% b) 2, 4-dichloro-6-methylthieno[2, 3-dJpyrimidine; According to Scheme 10 Step 2: 6-methylthieno[2,3-d]pyrimidine-2,4(lH,5H)-dione (0.89Og, 0.488mmol) was added by portion into phosphorous oxychloride (5.92ml, 63.5mmol) for 20min. The mixture was stirred at r.t for 10 minutes, then pyridine (9.77mmol) was added dropwise for 5min. The mixture was then heated at 110C for 45min. The excess of phosphorous oxychloride was removed in vacuo and the residue was taken up in dichloromethane and quickly washed with cold water. The organic phase was dried over MgSO4, filtered, and evaporated till dryness, yielding crude title compound as a brown solid, (0.79Og, 74%).
21% With N,N-dimethyl-aniline; trichlorophosphate; at 80℃; for 12h; j00374j A mixture of compound B-50 (2.0 g, 11 mmol) and dimethylaniline (1.9 g, 16 mmol) in phosphorus oxychloride (272 mL) was stirred at 80 C for 12 hours. On completion, the mixture was concentrated, poured into water (40 mL) and extracted with ethyl acetate (2 x 50 mL). The combined organic phase was washed with brine (30 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The residue was purified by silica gel chromatography [petroleum ether: ethyl acetate = 5:11 to give compound B-51 (0.50 g, 21% yield) as a yellow solid. LCMS (J): tR=1.221 mi, (ES+) mlz (M+H)+ 241.2
With trichlorophosphate; at 150℃; for 3h; EXAMPLE 16 2,4-Dichloro-6-methylthieno[2,3-d]pyrimidine; 6-Methylthieno[2,3-d]pyrimidine-2,4(1 H,3H)-dione (Example 10, 2.0 g) and POCI3 were heated together in a sealed tube at 150 0C for 3 hours. The mixture was then cooled and concentrated under reduced pressure and the residue was partitioned between dichlorom ethane and aqueous saturated sodium bicarbonate. The organic layer was dried over MgSO4, filtered and concentrated. The residue was triturated with diethyl ether containing a small amount of acetonitrile and the resulting solid was collected and dried under reduced pressure to give the title compound (1.75 g). MS (ESI+) m/z219.05 (M+H)+.
With 2,3-Dimethylaniline; trichlorophosphate; at 140℃; for 12h; Example 8b: 2,4-dichloro-6-methylthieno[2,3-d]pyrimidine; [0326] Example 8a (500mg, 2.75mmol, leq) was dissolved in Phosphorus oxychloride (200ml) containing l%v/v of Dimethylaniline in a high pressure reaction vessel. The solution was heated to 14O0C for 12 hours. Product was confirmed by LCMS. The phosphorus oxychloride was removed in vacuo and the residue co-evaporated with toluene (3x100ml) to leave 1.03g of approximately 60% pure product, which was used without further purification. [M+H] calc'd for C7H4CL2N2S, 219; found, 219.

  • 2
  • [ 124-38-9 ]
  • [ 138564-58-6 ]
  • [ 76872-71-4 ]
YieldReaction ConditionsOperation in experiment
88% With 1,5-diazabicyclo[4.3.0]non-5-ene 2,2,2-trifluoroethanol; at 90℃; for 48h; Compound 1j (1 mmol, 138 mg), [HDBN+][TFE-] (6 mmol, 1.35 g) was added to a 10 ml round bottom flask. In a CO2 environment, the reaction was heated to 90C for 48 hours, the reaction was stopped, the temperature was cooled to room temperature, and a saturated aqueous solution of NH4Cl was added. Adjust the pH to neutral, extract three times with 20ml CH2Cl2, collect the CH2Cl2 solution and dry it over anhydrous sodium sulfate. After filtration, the solution was removed by evaporation under reduced pressure, and the resulting solid was separated by silica gel column chromatography (eluent: CH2Cl2:CH3OH=15:1).160 mg of pale yellow solid Compound 2j, yield 88%.
88% With 1,5-diazabicyclo[4.3.0]non-5-ene 2,2,2-trifluoroethanol; at 90℃; under 760.051 Torr; for 48h;Green chemistry; General procedure: Substrate (1.0 mmol), [HDBN+][TFE-] (6.0 mmol) were loaded in a 10 mL glass reaction tube equipped with a magnetic stirrer. The air in the reactor was replaced by CO2. Then, the reactor was stirred at the desired temperature for 3-96 h under CO2 using a balloon. After the reaction, the reaction liquid was cooled to room temperature and quenched by saturated ammonium chloride solution. Then the mixture was filtered to afford the crude product, which was purified by chromatography (silica gel, methanol/dichloromethane=1/20) to give the desired compound. The purified product was characterized by NMR and HR-MS. 1H NMR and 13C NMR studies were carried out with a JEOL NMR 400 (400 MHz, 100 MHz) spectrometer with DMSO-d6 as the solvent. Mass spectra were recorded with an AMD40223(Interambulacra) spectrometer.
 

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