Home Cart 0 Sign in  

[ CAS No. 1073560-68-5 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 1073560-68-5
Chemical Structure| 1073560-68-5
Structure of 1073560-68-5 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 1073560-68-5 ]

Related Doc. of [ 1073560-68-5 ]

Alternatived Products of [ 1073560-68-5 ]

Product Details of [ 1073560-68-5 ]

CAS No. :1073560-68-5 MDL No. :MFCD32197258
Formula : C47H52N4O7 Boiling Point : -
Linear Structure Formula :- InChI Key :GZMLKDJDSMXRGP-HCVICXAGSA-N
M.W : 784.94 Pubchem ID :138911354
Synonyms :
Chemical Name :(S)-2-((S)-1-((S)-2-((S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)propanamido)-2-cyclohexylacetyl)pyrrolidine-2-carboxamido)-3,3-diphenylpropanoic acid

Safety of [ 1073560-68-5 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1073560-68-5 ]

* 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 [ 1073560-68-5 ]

[ 1073560-68-5 ] Synthesis Path-Downstream   1~14

  • 1
  • [ 124-09-4 ]
  • [ 1073560-68-5 ]
  • C100H116N10O12 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 14h; 38 Example 38 dimer compound 8Compound a (160 mg, 0.2 mmol) was dissolved in 1 mL DMF and HATU (91 mg, 0.24 mmol) followed by addition of 1,6-diaminohexane (12 mg, 0.1 mmol) and diisoproplyethylamine (52 μL, 0.3 mmol). The reaction was stirred at room temperature for 14 hours. The reaction was diluted with EtOAc, washed 2x with saturated NaHCO3 and washed with brine. Dried over MgSO4 and concentrated. The residue was dissolved in 2 mL DMF followed by the addition of 4- aminomethylpiperidine (120 μL, 1.0 mmol) and stirred at room temperature for 3 hours. Preparative HPLC gave compound 8. MS = 1205.2 (M+l).
  • 2
  • [ 1073560-68-5 ]
  • [ 109-76-2 ]
  • C97H110N10O12 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; HATU In N,N-dimethyl-formamide at 20℃; for 14h; 39 Example 39 dimer compound 9 Compound a (135 mg, 0.17 mmol) was dissolved in 1 mL DMF, HATU (91 mg, 0.24 mmol) was added followed by 1 ,6-diaminopropane (8 μL, 0.09 mmol) and diisoproplyethylamine (44 μL, 0.26 mmol). The reaction was stirred at room temperature for 14 hours. The reaction was diluted with EtOAc, washed 2x with saturated NaHCθ3 and washed with brine. Dried over MgSθ4 and concentrated. The residue was dissolved in 2 mL DMF followed by the addition of 4- aminomethylpiperidine (104 μL, 0.85 mmol) and stirred at room temperature for 3 hours. Preparative HPLC gave compound 8. MS = 1164.5 (M+l).
  • 3
  • C35H41N3O4 [ No CAS ]
  • [ 1073560-68-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 15 h / 20 °C 2: palladium on activated charcoal; hydrogen / 1,4-dioxane / 6.5 h / 20 °C 3: trifluoroacetic acid / dichloromethane / 3.5 h / 20 °C 4: potassium carbonate / tetrahydrofuran / 3 h / 20 °C
  • 4
  • [ 1384275-58-4 ]
  • [ 1073560-68-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: palladium on activated charcoal; hydrogen / 1,4-dioxane / 6.5 h / 20 °C 2: trifluoroacetic acid / dichloromethane / 3.5 h / 20 °C 3: potassium carbonate / tetrahydrofuran / 3 h / 20 °C
  • 5
  • C32H42N4O5 [ No CAS ]
  • [ 28920-43-6 ]
  • [ 1073560-68-5 ]
YieldReaction ConditionsOperation in experiment
56% With potassium carbonate In tetrahydrofuran at 20℃; for 3h;
  • 6
  • [ 1073560-68-5 ]
  • [ 1384275-65-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 20 h / 20 °C 2: hydrogenchloride / 1,4-dioxane / 1 h / 20 °C
  • 7
  • [ 1073560-68-5 ]
  • [ 153086-78-3 ]
  • C58H74N6O10 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride In dichloromethane at 20℃; for 20h;
  • 8
  • [ 1384275-60-8 ]
  • [ 1073560-68-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: trifluoroacetic acid / dichloromethane / 3.5 h / 20 °C 2: potassium carbonate / tetrahydrofuran / 3 h / 20 °C
  • 9
  • [ 1384275-51-7 ]
  • [ 1073560-68-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 8 steps 1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 22 h / 20 °C 2: hydrogenchloride / 1,4-dioxane / 4.5 h / 20 °C 3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 13 h / 20 °C 4: hydrogenchloride / 1,4-dioxane / 4.5 h / 20 °C 5: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 15 h / 20 °C 6: palladium on activated charcoal; hydrogen / 1,4-dioxane / 6.5 h / 20 °C 7: trifluoroacetic acid / dichloromethane / 3.5 h / 20 °C 8: potassium carbonate / tetrahydrofuran / 3 h / 20 °C
  • 10
  • [ 1384275-54-0 ]
  • [ 1073560-68-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 7 steps 1: hydrogenchloride / 1,4-dioxane / 4.5 h / 20 °C 2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 13 h / 20 °C 3: hydrogenchloride / 1,4-dioxane / 4.5 h / 20 °C 4: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 15 h / 20 °C 5: palladium on activated charcoal; hydrogen / 1,4-dioxane / 6.5 h / 20 °C 6: trifluoroacetic acid / dichloromethane / 3.5 h / 20 °C 7: potassium carbonate / tetrahydrofuran / 3 h / 20 °C
  • 11
  • C27H28N2O3 [ No CAS ]
  • [ 1073560-68-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 6 steps 1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 13 h / 20 °C 2: hydrogenchloride / 1,4-dioxane / 4.5 h / 20 °C 3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 15 h / 20 °C 4: palladium on activated charcoal; hydrogen / 1,4-dioxane / 6.5 h / 20 °C 5: trifluoroacetic acid / dichloromethane / 3.5 h / 20 °C 6: potassium carbonate / tetrahydrofuran / 3 h / 20 °C
  • 12
  • [ 1384275-56-2 ]
  • [ 1073560-68-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 5 steps 1: hydrogenchloride / 1,4-dioxane / 4.5 h / 20 °C 2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 15 h / 20 °C 3: palladium on activated charcoal; hydrogen / 1,4-dioxane / 6.5 h / 20 °C 4: trifluoroacetic acid / dichloromethane / 3.5 h / 20 °C 5: potassium carbonate / tetrahydrofuran / 3 h / 20 °C
  • 13
  • [ 15761-39-4 ]
  • [ 1073560-68-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 8 steps 1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 22 h / 20 °C 2: hydrogenchloride / 1,4-dioxane / 4.5 h / 20 °C 3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 13 h / 20 °C 4: hydrogenchloride / 1,4-dioxane / 4.5 h / 20 °C 5: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 15 h / 20 °C 6: palladium on activated charcoal; hydrogen / 1,4-dioxane / 6.5 h / 20 °C 7: trifluoroacetic acid / dichloromethane / 3.5 h / 20 °C 8: potassium carbonate / tetrahydrofuran / 3 h / 20 °C
  • 14
  • [ 109183-71-3 ]
  • [ 1073560-68-5 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 6 steps 1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 13 h / 20 °C 2: hydrogenchloride / 1,4-dioxane / 4.5 h / 20 °C 3: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 15 h / 20 °C 4: palladium on activated charcoal; hydrogen / 1,4-dioxane / 6.5 h / 20 °C 5: trifluoroacetic acid / dichloromethane / 3.5 h / 20 °C 6: potassium carbonate / tetrahydrofuran / 3 h / 20 °C
Same Skeleton Products
Historical Records