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Chemical Structure| 6200-36-8 Chemical Structure| 6200-36-8

Structure of 6200-36-8

Chemical Structure| 6200-36-8

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Product Details of [ 6200-36-8 ]

CAS No. :6200-36-8
Formula : C8H6Cl2O2
M.W : 205.04
SMILES Code : O=C(Cl)OCC1=CC=C(Cl)C=C1
MDL No. :MFCD24141290

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Application In Synthesis of [ 6200-36-8 ]

* 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 [ 6200-36-8 ]

[ 6200-36-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6200-36-8 ]
  • [ 201150-73-4 ]
  • tert-butyl 5-((((p-chlorophenyl)methoxy)carbonyl)amino)-1,2,3,4-tetrahydroisoquinoline-2-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 1h; 5-Amino-3,4-dihydroisoquinolin-2(1H)-carboxylic acid tert-butyl ester (50 mmol) and DIPEA (100 mmol) were weighed in a reaction flask.Add 300ml of dichloromethane,P-chlorobenzyl chloroformate (51 mmol) was slowly added dropwise with stirring at room temperature, and the mixture was stirred at room temperature for 1 h.Stop the reaction and concentrate the reaction mixture.Ethyl acetate was added 70ml, washed with dilute aqueous hydrochloric acid (0.2-0.3N), and saturated brine, dried over anhydrous sodium sulfate, filtered, and concentrated to give the title compound, was used directly in the next step.
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 1h; step 1:Weighing 5-amino-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (50 mmol)And DIPEA (100 mmol) in the reaction flask,Add 300ml of dichloromethane,P-chlorobenzyl chloroformate (51 mmol) was slowly added dropwise with stirring at room temperature.After the drop,Stirring was continued for 1 h at room temperature.Stop the reaction,Concentrate the reaction mixture,Add 70 ml of ethyl acetate,Wash with dilute aqueous hydrochloric acid (0.2-0.3N) and saturated brine.Dry over anhydrous sodium sulfate,filter,Concentrated to (3,4-dihydroisoquinolin-2(1H)-carboxylic acid tert-butyl ester-5-yl)-carbamic acid p-chlorobenzyl ester,Used directly in the next step,
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 1h; 5-Amino-3,4-dihydroisoquinolin-2(1H)-carboxylic acid tert-butyl ester (50 mmol) and DIPEA (100 mmol) were weighed in a reaction flask.Add 300ml of dichloromethane,P-chlorobenzyl chloroformate (51 mmol) was slowly added dropwise with stirring at room temperature.After the drop,Stirring was continued for 1 h at room temperature.Stop the reaction,Concentrate the reaction mixture,Add 70 ml of ethyl acetate,Dilute hydrochloric acid solution (0.2-0.3N)Washed with saturated brine,Dry over anhydrous sodium sulfate,Filtered and concentrated to give the title compound.Used directly in the next step.
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 1h; Weigh 5-amino-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (50 mmol) and DIPEA (100 mmol) in a reaction flask, add 300 ml of dichloromethane, and slowly add dropwise at room temperature with stirring. Chlorobenzyl chloroformate (51 mmol) was added dropwise, stirring was continued for 1 h at room temperature, the reaction was stopped, the reaction mixture was concentrated, ethyl acetate (70 ml), diluted aqueous hydrochloric acid (0.2-0.3N) and brine Sodium is dried, filtered and concentrated (3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester-5-yl)-carbamic acid p-chlorobenzyl ester, used directly in the next step.
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 1h; Weighed 5-amino-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (50 mmol) and DIPEA (100 mmol) in a reaction flask, and added 300 ml of dichloromethane. The mixture was slowly added dropwise with p-chlorobenzyl chloroformate (51 mmol) at room temperature, and the mixture was stirred at room temperature for 1h, the reaction was stopped, the reaction mixture was concentrated, ethyl acetate (70 ml), diluted aqueous hydrochloric acid (0.2-0.3N) and saturated salt washed with water, dried over anhydrous sodium sulfate, filtered,concentrated to (3,4-dihydroisoquinolin-2(1H)-carboxylic acid tert-butyl ester-5-yl)-carbamic acid p-chlorobenzyl ester, used directly in the next step,

 

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