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Chemical Structure| 61533-68-4 Chemical Structure| 61533-68-4

Structure of 61533-68-4

Chemical Structure| 61533-68-4

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Product Details of [ 61533-68-4 ]

CAS No. :61533-68-4
Formula : C7H9ClN2O2
M.W : 188.61
SMILES Code : COCCOC1=CN=C(Cl)N=C1
MDL No. :MFCD26403410
Boiling Point : No data available

Safety of [ 61533-68-4 ]

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 [ 61533-68-4 ]

* 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 [ 61533-68-4 ]

[ 61533-68-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6482-24-2 ]
  • [ 4983-28-2 ]
  • [ 61533-68-4 ]
YieldReaction ConditionsOperation in experiment
85% With potassium carbonate; In N,N-dimethyl-formamide; at 50℃; for 16h;Inert atmosphere; j0399j 2-Chloropyrimidin-5-ol (200 mg, 1.53 mmol), 1-bromo-2-methoxyethane (0.158 mL, 1.69 mmol) and potassium carbonate (423.5 mg 3.06 mmol) were suspended in anhydrous NN-dimethylformamicle (5 mL) and heated 10 50 °C in a nitrogen almosphere for 16 hours. The solvents were removed in vacuo and the residue was partitioned between ethyl acetate (50 mL) and water (30 mL), the aqueous was extracted with ethyl acetate (2 x 30 niL) and the conbilled organics washed with brine (20 mL), dried over anhydrous sodium sulfate, filtered and concentrated to give the title compound 244 mg (yield 85percent) as off-white translucent crystals. &i NMR (500 MHz, DMSO) 8.55 (s, 2F1), 4.37 ?4.21 (m, 2H), 3.78 ? 3.59 (m, 2H), 3.30 (s, 3H). Tr(METCRI278) = 1.36 mill, (Est) (M+Na)t 189.
With potassium carbonate; In N,N-dimethyl-formamide; at 60℃; for 26h; To a stirred solution of 2-chloropyrimidm-5-ol (Intermediate No.86 Step 2, 17.5 g, 134 mmol) in DMF (90 mL was added 2-bromoethyl methyl ether (17.6 mL, 1-87 mmol) followed by K2C03 (24.0 g, 174 mmol). The. resulting suspension was heated at 60 °C for 18 hr. In order to drive the reaction to completion, additional 2-bromoethyl methyl ether (16.0 mL, 170 mmol) and K2C03 (18.5 g, 134 mmol) were added, and- the heating was continued for approximately 8 hr. The reaction mixture was cooled and partitioned between 10percent aqueous sodium chloride (250 mL) and EtOAc (500 mL). The layers were separated and the organic layer was washed with 10percent aqueous sodium chloride (250 mL). The first aqueous layer was extracted with EtOAc (250 mL). The second aqueous layer was salted with solid NaCl, and extracted with EtOAc (250-mL). The combined organic layers were driecLover Na2S04, filtered, andconcentrated to a crude oil that was taken up into a minimal amount of DCM and purified by silica gel chromatography to afford 2-chIoro-5-(2-methoxyethoxy)pyrimidine as a white solid. LRMS (ESI) calc'd for C7H10C1N2O2 [M+Hf: 189. ; found 189.
 

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