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Chemical Structure| 857904-02-0 Chemical Structure| 857904-02-0

Structure of 857904-02-0

Chemical Structure| 857904-02-0

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Product Details of [ 857904-02-0 ]

CAS No. :857904-02-0
Formula : C20H26N4O3
M.W : 370.45
SMILES Code : O=C(OC)N[C@@H](C(C)(C)C)C(NNCC1=CC=C(C2=NC=CC=C2)C=C1)=O
MDL No. :MFCD29920899

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Application In Synthesis of [ 857904-02-0 ]

* 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 [ 857904-02-0 ]

[ 857904-02-0 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 857904-02-0 ]
  • [ 1192510-20-5 ]
  • [ 198904-31-3 ]
YieldReaction ConditionsOperation in experiment
87% In dichloromethane; for 64h;Silica gel; Example 8; Atazanavir (1) A suspension of (2R,3S)-1,2-Epoxy-3-[N-(methoxycarbonyl)-L-tert-leucinyl]amino}-4-phenylbutane (2) (334 mg, 1 mmol), N-[N-(Methoxycarbonyl)-L-tert-leucinyl]-N'-[4-(2-pyridyl)phenylmethyl]hydrazine (3) (370 mg, 1 mmol) and silica gel (1.0 g) in CH2Cl2 (3 mL) was stirred for 64 h. The mixture was diluted with EtOAc (10 mL), filtered and washed with a mixture of EtOAc-CH2Cl2 (1:1). The filtrate was concentrated under reduced pressure. The residue was crystallized from EtOAc-hexane to give the product (613 mg, 87%) as colorless crystals.
87% silica gel; In dichloromethane; for 64h; A suspension of (2i?,3S)-l,2-Epoxy-3-[N-(methoxycarbonyl)-L-te/t- leucinyl] amino }-4-phenylbutane (2) (334 mg, 1 mmol), N-[N-(M ethoxycarbonyl)-L-te/t- leucinyl]-N'-[4-(2-pyridyl)phenylmethyl] hydrazine (3) (370 mg, 1 mmol) and silica gel (1.0 g) in CH2Cl2 (3 mL) was stirred for 64 h. The mixture was diluted with EtOAc (10 mL), filtered and washed with a mixture Of EtOAc-CH2Cl2 (1 : 1). The filtrate was concentrated under reduced pressure. The residue was crystallized from EtOAc-hexane to give the product (613 mg, 87%) as colorless crystals.
In isopropyl alcohol; at 90℃; for 12h; (102.0g, 305.0mmol) a compound of formula (S) -1 - (( S) -2-epoxy-2-ethyl-1-phenylethane - amino) -3,3-dimethyl Methyl-1-carbonylbutan-2-yl-carbamate and (122.2 g, 330.0 mmol) Compound N-1-[N-(methoxycarbonyl)-L-tert-leucine]-N- Dissolve 2-[4-(2-pyridyl)-benzyl]hydrazine in 500 ml of isopropanol, reflux at 90 C for 12 hours, cool, slowly add 1000 ml of distilled water, stir for 2 hours, stand, filter, wash and reuse. recrystallisation from aqueous ethanol, vacuum drying, the liquid phase is detected, to give 201.3g of formula compound 1- [4- (2-pyridyl) phenyl] -5 (S) -2,5- bis [N- (methyl oxygen-carbonyl) -L- tert-leucine-yl] amino} -4 (S) - hydroxy-6-phenyl-2-aza-hexane VIII, namely atazanavir.
  • 3
  • [ 857904-02-0 ]
  • 1-[4-(pyridin-2-yl)phenyl]-2,5-bis[N-(methoxycarbonyl)-L-tert-leucinyl]amino}-4(S)-hydroxy-6-phenyl-2-azahexane [ No CAS ]
  • [ 198904-31-3 ]
 

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