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Chemical Structure| 19358-41-9 Chemical Structure| 19358-41-9

Structure of 19358-41-9

Chemical Structure| 19358-41-9

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Product Details of [ 19358-41-9 ]

CAS No. :19358-41-9
Formula : C7H4Cl2O2
M.W : 191.01
SMILES Code : O=C(Cl)OC1=CC=CC=C1Cl
MDL No. :MFCD02093716

Safety of [ 19358-41-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H314-H331
Precautionary Statements:P261-P280-P305+P351+P338-P310
Class:6.1(8)
UN#:3277
Packing Group:

Application In Synthesis of [ 19358-41-9 ]

* 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 [ 19358-41-9 ]

[ 19358-41-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19358-41-9 ]
  • [ 201150-73-4 ]
  • (3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester-5-yl)carbamic acid o-chlorophenyl ester [ 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,O-chlorophenyl 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 and 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 (p-chlorophenyl ester of 3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester-5-yl)-carbamic acid,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, 300 ml of dichloromethane was added, and 2-Chlorophenyl chloroformate (51 mmol) was slowly added dropwise with stirring at room temperature, after the dropwise addition the mixture was stirred at room temperature for further 1 hour. The reaction was stopped, the reaction mixture was concentrated, ethyl acetate (70 ml) was added, then Washed with dilute aqueous hydrochloric acid (0.2-0.3N) and saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated to give (3,4-Dihydroisoquinoline-2 (1H)-carboxylic acid tert-butyl ester-5-yl)- Carbamic acid o-chlorophenyl ester, used directly in the next step.
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 1h; Weighing <strong>[201150-73-4]tert-butyl 5-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate</strong> (50 mmol) and DIPEA (100 mmol) in reaction bottle, adding dichloromethane 300 ml, stirring at the room temperature slowly o-chlorophenyl carbonochloridate (51 mmol), then completing, continuing stirring at room temperature 1 h, stopping the reaction, concentrating the reaction mixture, adding ethyl acetate 70 ml, dilute hydrochloric acid aqueous solution (0.2 - 0.3 N) and saturated salt water washing, anhydrous sodium sulfate drying, filtering, concentrated to obtain tert-butyl 5-[(2-chlorophenoxy)carbonyl]amino}-3,4-dihydroisoquinoline-2(1H)-carboxylate, directly used in the next step
 

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