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Chemical Structure| 7693-45-0 Chemical Structure| 7693-45-0

Structure of 7693-45-0

Chemical Structure| 7693-45-0

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Product Details of [ 7693-45-0 ]

CAS No. :7693-45-0
Formula : C7H4Cl2O2
M.W : 191.01
SMILES Code : O=C(Cl)OC1=CC=C(Cl)C=C1
MDL No. :MFCD00000638
InChI Key :RYWGPCLTVXMMHO-UHFFFAOYSA-N
Pubchem ID :139059

Safety of [ 7693-45-0 ]

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

Application In Synthesis of [ 7693-45-0 ]

* 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 [ 7693-45-0 ]

[ 7693-45-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7693-45-0 ]
  • [ 201150-73-4 ]
  • (3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester-5-yl)carbamic acid p-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,P-chlorophenyl 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. Add 70 ml of ethyl acetate, dilute aqueous hydrochloric acid (0.2-0.3 N) and brine, and dry over anhydrous sodium sulfate. Filtration and concentration to give (3,4-dihydroisoquinolin-2(1H)-carboxylic acid tert-butyl-5-yl)-carbamic acid p-chlorophenyl ester directly to the next step.
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 1h; Weigh out 5-amino-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (50 mmol)And DIPEA (100 mmol) in a reaction flask, adding 300 ml of dichloromethane,P-chlorophenyl chloroformate (51 mmol) was slowly added dropwise with stirring at room temperature.After the completion of the dropwise addition, stirring was continued for 1 h at room temperature to stop the reaction.The reaction mixture was concentrated, and ethyl acetate (70 ml) was added.Wash with dilute aqueous hydrochloric acid (0.2-0.3N) and saturated brine.Dry over anhydrous sodium sulfate, filter,And concentrated to give (3,4-dihydro-isoquinoline -2(1H)-tert-butyl-5-yl)-carbamic acid p-chlorophenyl ester,Used directly in the next step,
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 1h; Weighing 5-amino-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (50 mmol)And DIPEA (100 mmol) in a reaction flask, adding 300 ml of dichloromethane,The p-chlorophenyl chloroformate (51 mmol) was slowly added dropwise with stirring at room temperature.Stirring was continued for 1 h at room temperature, the reaction was stopped, and the reaction mixture was concentrated.Add 70 ml of ethyl acetate,Wash with dilute aqueous hydrochloric acid (0.2-0.3N) and saturated brine, dry over anhydrous sodium sulfate.Filtered and concentrated(3,4-Dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester-5-yl)-p-chlorophenyl ester, used directly in the next step
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 1h; Weighing 5-amino-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (50 mmol)And DIPEA (100 mmol) in a reaction flask, adding 300 ml of dichloromethane,The p-chlorophenyl chloroformate (51 mmol) was slowly added dropwise with stirring at room temperature.Stirring was continued for 1 h at the temperature, the reaction was stopped, and the reaction mixture was concentrated.Add 70 ml of ethyl acetate, dilute aqueous hydrochloric acid (0.2-0.3 N) 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,
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 1h; Step 1: Weigh out 5-amino-3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester (50 mmol)And DIPEA (100 mmol) in a reaction flask, adding 300 ml of dichloromethane,p-chlorophenyl chloroformate (51 mmol) was slowly added dropwise with stirring at room temperature, and the mixture was stirred at room temperature for 1 h.The reaction was stopped, the reaction mixture was concentrated, ethyl acetate was added 70ml, washed with dilute aqueous hydrochloric acid (0.2-0.3N), and saturated brine,Dry over anhydrous sodium sulfate, filter,Concentration (3,4-dihydroisoquinoline-2(1H)-carboxylic acid tert-butyl ester-5-yl)-carbamic acid p-chlorophenyl ester, directly used in the next step,

 

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