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Chemical Structure| 1440519-63-0 Chemical Structure| 1440519-63-0

Structure of 1440519-63-0

Chemical Structure| 1440519-63-0

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Product Details of [ 1440519-63-0 ]

CAS No. :1440519-63-0
Formula : C10H10ClNO
M.W : 195.65
SMILES Code : O=C1NC(C)(C)C2=C1C=CC(Cl)=C2
MDL No. :MFCD26407089
InChI Key :DQVCNEFERHUONP-UHFFFAOYSA-N
Pubchem ID :71743949

Safety of [ 1440519-63-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 1440519-63-0 ]

* 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 [ 1440519-63-0 ]

[ 1440519-63-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 53710-18-2 ]
  • [ 1440519-63-0 ]
  • 5-chloro-2-(5-iodopyridin-3-yl)-3,3-dimethyl-2,3-dihydroisoindol-1-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
36% With potassium phosphate; copper(l) iodide; trans cyclohexane-1,2-diamine; In 1,4-dioxane; at 110℃; for 2h;Inert atmosphere; A mixture of 5-chloro-3 ,3-dimethyl-2,3-dihydro-isoindol- 1-one (intermediate A-3) (2.3 g,11.8 mmol), <strong>[53710-18-2]3,5-diiodo-pyridine</strong> (example 7[A]) (6.9 g, 21 mmol), CuT (673 mg, 3.54mmol), K3P04 (5.0 g, 23.6 mmol) and trans-cyclohexane- 1 ,2-diamine (810 mg, 7.1 mmol) in dioxane (50 mL) was stuffed at 110C for 2 hours. The reaction was filtered and the filtrate was concentrated under reduced pressure to give a crude solid which was purified by flash chromatography to give the title product as a white solid (1.7 g, 36%). MS: 398.7(M+H).
1.8 g With potassium phosphate; copper(l) iodide; (S,S)-1,2-diaminocyclohexane; In 1,4-dioxane; at 120℃; for 3h;Sealed tube; Inert atmosphere; In a 75-mL sealed tube, <strong>[53710-18-2]3,5-diiodo-pyridine</strong> (intermediate A-5, 6.6 g, 20 mmol), 5-chloro- 3,3-dimethyl-2,3-dihydro-isoindol-1-one (intermediate A-3, 1.95 g, 10 mmol), CuT (571 mg, 3 mmol), K3P04 (4.24 g, 20 mmol) and (+)-(S,S)-1,2-diaminocyclohexane (0.7 mL, 6 mmol) were dissolved in 20 mL of dioxane. The resulting reaction mixture was heated at120C for 3 hours before it was poured into water (50 mL) and extracted with EtOAc (2 x125 mL). The combined organic layers were washed with brine, dried over anhy. Na2SO4,filtered and concentrated in vacuo to give a crude product, which was purified by silica gelflash chromatography (0-30% EtOAc-hexane gradient) to yield the title compound (1.8 g,45%) as a light yellow solid. MS: 399.2 (M+Hj.
1.8 g With potassium phosphate; copper(l) iodide; (S,S)-1,2-diaminocyclohexane; In 1,4-dioxane; at 120℃; for 3h;Sealed tube; Inert atmosphere; In a 75-mL sealed tube, <strong>[53710-18-2]3,5-diiodo-pyridine</strong> (intermediate A-5, 6.6 g, 20 mmol), 5-chloro- 3,3-dimethyl-2,3-dihydro-isoindol-1-one (intermediate A-3, 1.95 g, 10 mmol), CuT (571 mg, 3 mmol), K3P04 (4.24 g, 20 mmol) and (+)-(S,S)-1,2-diaminocyclohexane (0.7 mL, 6 mmol) were dissolved in 20 mL of dioxane. The resulting reaction mixture was heated at120C for 3 hours before it was poured into water (50 mL) and extracted with EtOAc (2 x125 mL). The combined organic layers were washed with brine, dried over anhy. Na2SO4, filtered and concentrated in vacuo to give a crude product, which was purified by silica gel flash chromatography (0-30% EtOAc-hexane gradient) to yield the title compound (1.8 g, 45%) as a light yellow solid. MS: 399.2 (M+H).
 

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