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Chemical Structure| 35849-31-1 Chemical Structure| 35849-31-1

Structure of 35849-31-1

Chemical Structure| 35849-31-1

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Product Details of [ 35849-31-1 ]

CAS No. :35849-31-1
Formula : C9H11ClN2O
M.W : 198.65
SMILES Code : O=C1NC2=C(C=CC=C2)CC1N.[H]Cl
MDL No. :MFCD09999258

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Application In Synthesis of [ 35849-31-1 ]

* 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 [ 35849-31-1 ]

[ 35849-31-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7732-18-5 ]
  • [ 35849-31-1 ]
  • [ 49827-15-8 ]
  • [ 98626-39-2 ]
YieldReaction ConditionsOperation in experiment
With NaH; In tetrahydrofuran; ethyl acetate; A. t-Butoxycarbonylmethyl-3-aminodihydrocarbostyril STR5 To a suspension of 2.42 gm NaH (50percent oil dispersion washed 3*hexanes) in 50 ml of THF at 0° C. was added solid 5 gm (0.025 mol) of 3-aminodihydrocarbostyrilhydrochloride (T. J. McCord, Arch. of Biochem. and Biophys. 102 48 (1963)) stirring at 0° C. until the evolution of hydrogen had ceased at which time the reaction mixture was warmed to room temperature and stirred a further 1 hour. To the stirred reaction mixture was added dropwise a solution of 6 gm of <strong>[49827-15-8]t-butyl iodoacetate</strong> in 20 ml of THF stirring a further 2 hours at room temperature at which time the reaction was quenched with 20 ml of saturated NaHCO3. The reaction mixture was diluted with 20 ml of H2 O and extracted 2*50 ml of 9:1 ethylacetate:acetonitrile. The organic layers were combined, filtered through MgSO4 and concentrated in vacuo to give 5 gm of 1-t-butoxycarbonylmethyl-3 -aminodihydrocarbostyril. NMR (CDCl3, TMS): 1.4 (s, 9H); 2.0-3.2 (m, 4H), 3.4-3.8 (m, 1H); 4.6 (Q, 2H); 6.6-7.2 (m, 4H).
With NaH; In tetrahydrofuran; EXAMPLE 17 Preparation of t-butoxycarbonylmethyl-3-aminodihydrocarbostyril STR54 To a suspension of 2.42 gm NaH (50percent oil dispersion washed 3*hexanes) in 50 ml of THF at 0° C. was added solid 5 gm (0.025 mol) of 3-aminodihydrocarbostyrilhydrochloride (T. J. McCord, Arch. of Biochem. and Biophys. 102 48, 1963) and the mixture was stirred at 0° C. until the evolution of hydrogen had ceased. When the evolution stopped, the reaction mixture was warmed to room temperature and stirred an additional 1 hour, at which time a solution of 6 gm of <strong>[49827-15-8]t-butyl iodoacetate</strong> in 20 ml of THF was added dropwise. After an additional two hours of stirring at room temperature, the reaction was quenched with 20 ml of saturated NaHCO3, and the reaction mixture was diluted with 20 ml of H2 O and extracted twice with 50 ml of 9:1 ethylacetate:acetonitrile. The organic layers were combined, filtered through MgSO4 and concentrated in vacuo to give 5 gm of 1-t-butoxycarbonylmethyl-3 -aminodihydrocarbostyril. NMR (CDCl3, TMS) 1.4 (s, 9H); 2.0-3.2 (m, 4H), 3.4-3.8 (m, 1H); 4.6 (Q, 2H); 6.6-7.2 (m, 4H).
With NaH; In tetrahydrofuran; ethyl acetate; A. t-Butoxycarbonylmethyl-3-aminodihydrocarbostyril STR7 To a suspension of 2.42 gm NaH (50percent oil dispersion washed 3 *hexanes) in 50 ml of THF at 0° C. was added solid 5 gm (0.025 mol) of 3-aminodihydrocarbostyrilhydrochloride (T. J. McCord, Arch. of Biochem. and Biophys. 102 48 (1963)) stirring at 0° C. until the evolution of hydrogen had ceased at which time the reaction mixture was warmed to room temperature and stirred a further 1 hour. To the stirred reaction mixture was added dropwise a solution of 6 gm of <strong>[49827-15-8]t-butyl iodoacetate</strong> in 20 ml of THF stirring a further 2 hours at room temperature at which time the reaction was quenched with 20 ml of saturated NaHCO3. The reaction mixture was diluted with 20 ml of H2 O and extracted 2*50 ml of 9:1 ethylacetate:acetonitrile. The organic layers were combined, filtered through MgSO4 and concentrated in vacuo to give 5 gm of 1-t-butoxycarbonylmethyl- 3-aminodihydrocarbostyril. NMR (CDCl3, TMS) 1.4 (s, 9H); 2.0-3.2 (m, 4H), 3.4-3.8 (m, 1H); 4.6 (Q, 2H); 6.6-7.2 (m, 4H) IR C=O 1738, 1680
 

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