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Chemical Structure| 850424-11-2 Chemical Structure| 850424-11-2

Structure of 850424-11-2

Chemical Structure| 850424-11-2

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Product Details of [ 850424-11-2 ]

CAS No. :850424-11-2
Formula : C9H7ClN2O
M.W : 194.62
SMILES Code : COC1=CC2=CN=C(Cl)N=C2C=C1
MDL No. :MFCD17215768

Safety of [ 850424-11-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 850424-11-2 ]

* 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 [ 850424-11-2 ]

[ 850424-11-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 850424-11-2 ]
  • [ 5369-19-7 ]
  • [ 850424-15-6 ]
  • 2
  • [ 105763-77-7 ]
  • [ 850424-11-2 ]
YieldReaction ConditionsOperation in experiment
71% With ammonia; zinc; In dichloromethane; water; at 40℃; for 4h;Inert atmosphere; To a solution of 2,4-dichloro-6- methoxyquinazoline (3 g, 13.1 mmol) in dichloromethane (50 mL) were added zinc dust (2.57 g, 39.3 mmol), aqueous solution of ammonia (50 mL, 34% w/w) and brine (10 mL). The resulting mixture was stirred for 4 hours at 40 C under nitrogen atmosphere. After cooling down to ambient temperature, the resulting mixture was filtered through Celite. The organic layer was collected and the aqueous layer was extracted with dichloromethane (2 x 50 mL). The combined organic layers was dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography, eluted with 1-2% methanol in dichloromethane to afford 2-chloro-6- methoxyquinazoline as a yellow solid: MS (ESI, m/z): 195.2 [M + 1]+; 1H MR (300 MHz, CDC13) delta 9.19 (s, 1H), 7.91 (d, J= 9.3 Hz, 1H), 7.61 (dd, J= 2.7 Hz, 6.6 Hz, 1H), 7.16 (d, J = 2.7 Hz, 1H), 3.96 (s, 3H).
68% To a solution of 2,4- dichloro-6-methoxyquinazoline (400 mg, 1.75 mmol) in CH2C12 (10 mL) was added brine (10 mL) containing 9% NuEta32Omicron. Then zinc powder (336 mg, 5.25 mmol) was added and the mixture was refluxed for 2 hours. The mixture was diluted with CH2C12 (50 mL) and filtered off, the filtrate was neutralized by 2M HC1 to pH 7. The aqueous layer extracted with CH2C12 (20 mL x2), the combined organic layer washed with brine (30 mL), dried over Na2S04, filtered and concentrated to give the crude product, which was purified by silica gel column (PE / EtOAc=5 / 1) to give Intermediate 8 (232 mg, yield 68%). *H NMR (CDC13 300 MHz): delta 9.20 (s, 1H), 7.90 (d, J = 9.3 Hz, 1H), 7.40 (dd, J = 9.3, 2.7 Hz, 1H), 7.15 (d, J = 3.0 Hz, 1H), 3.95 (s, 3H).
24% With ammonium hydroxide; sodium chloride; zinc; In dichloromethane; water; at 50℃; for 48h; To a solution of <strong>[105763-77-7]2,4-dichloro-6-methoxyquinazoline</strong> (880 mg, 3.8 mmol) in sat. NaCl (10 mL) and DCM (15 mL) was added NH4OH (4.5 mL) and Zn (750 mg, 11.5 mmol). The reaction mixture was stirred at 50 C for 2 days. The mixture was diluted with water (100 mL) and extracted with DCM (100 mL*2). The combined organic layers were dried over Na2S04, filtered and (0611) concentrated. The residue was purified by silica gel chromatography (PE/EA, 5: 1) to afford 2- chloro-6-methoxyquinazoline (180 mg, 24%) as a yellow solid. 1H NMR (400 MHz, CDCI3): d 3.97 (s, 3H), 7.17 (d, J= 2.8 Hz, 1H), 7.60 (dd, 7= 3.2, 9.2 Hz 1H), 7.90 (d, J= 9.2 Hz, 1H), 9.20 (s, 1H).
 

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