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Chemical Structure| 66729-00-8 Chemical Structure| 66729-00-8

Structure of 66729-00-8

Chemical Structure| 66729-00-8

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Product Details of [ 66729-00-8 ]

CAS No. :66729-00-8
Formula : C9H7ClN2
M.W : 178.62
SMILES Code : NC1=C(Cl)C2=C(C=N1)C=CC=C2
MDL No. :MFCD13193664

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Application In Synthesis of [ 66729-00-8 ]

* 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 [ 66729-00-8 ]

[ 66729-00-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 66729-00-8 ]
  • [ 25475-67-6 ]
  • 2
  • [ 25475-67-6 ]
  • [ 66729-00-8 ]
YieldReaction ConditionsOperation in experiment
84% With N-chloro-succinimide; In methanol; at 20℃; for 3h; To <strong>[25475-67-6]isoquinolin-3-amine</strong> (2.02 g, 14.0 mmol) inmethanol (60 mL) was added N-chlorosuccinimide (2.19 g,16.4 mmol) at room temperature. The reaction was stirred atroom temperature for 3 hours, then concentrated in vacuo.The crude material was chromatographed (Biotage: 10-100percentethyl acetate/hexanes) to yield 4-chloro<strong>[25475-67-6]isoquinolin-3-amine</strong>(2.1 g, 11.8 mmol, 84percent yield) as a solid.
20.52 g With 1,3-dichloro-5,5-dimethylhydantoin; Isopropyl acetate; at -10℃; for 16h; Isoquinolin-3-amine (25.01 g) (1),Isopropyl acetate (250 mL) was mixed,1,3-Dichloro-5,5-dimethylhydantoin (40.09 g) was added at -10 ° C. and the mixture was stirred for about 16 hours.After raising the temperature to 10 ° C., a 0.6N hydrochloric acid aqueous solution (250 mL) was added dropwise,After filtration with foreign matter, it was washed with water (50 mL).Precoated with activated charcoal (2.5 g), washed with water (50 mL), and separated. A 2 N hydrochloric acid aqueous solution (75 mL) was added to the organic layer, and the mixture was stirred and then separated. The aqueous layer was mixed and 2N sodium hydroxide aqueous solution (175 mL) was added dropwise at 10 ° C.Precipitated crystals were collected by filtration and washed with water (125 mL). The obtained crystals, water (158 mL), 2 N hydrochloric acid aqueous solution (68 mL) and toluene (100 mL) were mixed and after pre-coat filtration with activated carbon (2.0 g), washed with water (50 mL) It was liquid.A 2N sodium hydroxide aqueous solution (140 mL) was added dropwise at 10 ° C.The precipitated crystals were collected by filtration, washed with water (125 mL), and dried under reduced pressure to obtain 4-chloro<strong>[25475-67-6]isoquinolin-3-amine</strong> (2) (20.52 g, yellow crystals).
 

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