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Chemical Structure| 362057-20-3 Chemical Structure| 362057-20-3

Structure of 362057-20-3

Chemical Structure| 362057-20-3

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Product Details of [ 362057-20-3 ]

CAS No. :362057-20-3
Formula : C12H12N2O2
M.W : 216.24
SMILES Code : O=C(C1=CC2=C(C=N1)C=CC=C2)N(OC)C

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Application In Synthesis of [ 362057-20-3 ]

* 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 [ 362057-20-3 ]

[ 362057-20-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6624-49-3 ]
  • [ 1117-97-1 ]
  • [ 362057-20-3 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In dichloromethane; for 18h;Product distribution / selectivity; Step 1: Isoquinoline-3-carboxylic acid methoxy-methyl-amide 2.46 g (12.9 mmol) of <strong>[6624-49-3]isoquinoline-3-carboxylic acid</strong> hydrate was dissolved in 100 mL dichloromethane under room temperature. 1.38 g (14.1 mmol) of methoxymethyl amine was added followed by addition of 4.55 g (15.5 mmol) of 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride and 1.44 g (14.1 mmol) of triethylamine. The reaction was stirred for 18 hour and 250 ml of water was added. The organic layer was dried over anhydrous magnesium sulfate and evaporated in vacuum. Purification using flash chromatography, elution with 100percent ethyl acetate yielded to 2.70 g of product as colorless solid. LC-MSD, m/z for C14H25NO3 [M+H]+: 217.3, [M+2H]+: 218.3. LC retention time on HPLC, C18 column gradient 20-95percent acetonitrile with 0.1percent TFA in 4 min: 0.492 min.
  • 2
  • [ 6624-49-3 ]
  • [ 6638-79-5 ]
  • [ 362057-20-3 ]
YieldReaction ConditionsOperation in experiment
67% With N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; triethylamine; In dichloromethane; at 20℃; for 3h; Example 1 Production of N-benzyl-2-[3-benzyl-3,4-dihydroisoquinolin-2(1H)-yl]ethanamine a) Production of N-methoxy-N-methylisoquinoline-3-carboxyamide [Show Image]; 200 mg of <strong>[6624-49-3]3-isoquinolinecarboxylic acid</strong>, 169 mg of N,O-dimethylhydroxylamine monohydrochloride, 332 mg of WSC, and 582 mg of triethylamine were dissolved in 2 mL of dichloromethane, followed by stirring at room temperature for 3 hours. Water was added to the reaction liquid, followed by extraction with chloroform. The organic layer was then washed with saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The residue obtained was purified using silica gel chromatography (chloroform alone) to obtain 169 mg (yield 67percent) of a title compound as a pale yellow solidified product. 1H-NMR (CDCl3) delta: 3.47 (3H, s), 3.80 (3H, s), 7.69 (1H, ddd, J = 1.2, 8.0, 8.0 Hz), 7.76 (1H, ddd, J =1.2, 8.0, 8.0 Hz), 7.92 (1H, d, J = 8.0 Hz), 8.02 (1H, d, J = 8.0 Hz), 8.14 (1H, s), 9.25 (1H, s).
With triethylamine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride; In acetonitrile; for 48h;Product distribution / selectivity; Step 1: Isoquinoline-3-carboxylic acid methoxy-methyl-amide In 50 mL of acetonitrile was dissolved 0.49 g (2.60 mmol) of <strong>[6624-49-3]isoquinoline-3-carboxylic acid</strong> monohydrate. To this 0.28 g (2.87 mmol) of O,N-dimethyl-hydroxylamine hydrochloride, 0.4 mL (2.87 mmol) triethylamine and 0.921 g (3.13 mmol) of 4-(4,6-dimethoxy-[1,3,5]triazin-2-yl)-4-methyl-morpholin-4-ium chloride hydrate were added and stirred for 2 days and then evaporated. A mixture of dichloromethane and water was added to it and the organic layer was evaporated and purified using flash chromatography (0-20percent methanol in dichloromethane). Fractions containing pure product were evaporated to yield 210 mg of the free base as a white solid. LC-MSD, m/z for C12H12N2O2 [M+H]+: 217.4, [M+Na]+: 239.4
 

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