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Chemical Structure| 5129-22-6 Chemical Structure| 5129-22-6

Structure of 5129-22-6

Chemical Structure| 5129-22-6

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Product Details of [ 5129-22-6 ]

CAS No. :5129-22-6
Formula : C9H13NO
M.W : 151.21
SMILES Code : OCC1=CC=C(CC)C(N)=C1
MDL No. :MFCD28129087

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Application In Synthesis of [ 5129-22-6 ]

* 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 [ 5129-22-6 ]

[ 5129-22-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5129-22-6 ]
  • [ 7205-46-1 ]
  • [ 1449514-94-6 ]
YieldReaction ConditionsOperation in experiment
With dibenzylideneacetone bis(triphenylphiosphine) palladium(0); 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; sodium t-butanolate; In N,N-dimethyl-formamide; at 120.0℃; for 16h; A mixture of 6-chloro-l-methyl-lH-imidazo[4,5-c]pyridine (intermediate 2) (84 mg, 0.5 mmol), 7-methyl-2,3-dihydrobenzo[6][l,4]dioxin-6-amine ( 1 .5 eq. ) , dib enzylidene ac etone bis(triphenylphiosphine) palladium (0) (5mol.%), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (10 mol.%), sodium tert-butoxide (1.5 eq.) and DMF (0.33 M) is stirred at 120 C for 16 h. The reaction mixture is allowed to cool to room temperature, filtered and the solvent removed in vacuo. The crude product is purified by preparative HPLC to afford the desired product. (4-ethyl-3-(l-methyl-lH-imidazo[4,5-c]pyridin-6-ylamino)phenyl)methanol was obtained by reacting (3-Amino-4-ethylphenyl)methanol with 6-chloro-l-methyl-lH-imidazo[4,5-c]pyridine according to method A" described above
With tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; sodium t-butanolate; In 1,4-dioxane; at 100.0℃; for 7h;Inert atmosphere; To stirred degassed (N2) 1,4-dioxane (30 mL) was added (3-amino-4-ethylphenyl)MeOH (440 mg, 2.90 mmol), 6-chloro-l -methyl-lH-imidazo[4,5-c] pyridine (480 mg, 2.9 mmo l) , tris(dibenzylideneacetone)dipalladium(0) (0.12 mg, 0.145 mmol), 4,5-bis(diphenylphosphino)-9,9- dimethylxanthene (160 mg, 0.29 mmol) and sodium tert-butoxide (690 mg, 0.725 mmol). The reaction mixture was heated to 100 C for 7 h, cooled to room temperature, concentrated in vacuo and ethyl acetate and water were added. The ethyl acetate was separated, dried (MgSO i), filtered and concentrated in vacuo. The residue was dissolved in MeOH and loaded onto a 20 g SCX cartridge which was washed with MeOH and eluted with dilute ammonia in MeOH to give the desired compound.
 

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