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Chemical Structure| 61424-26-8 Chemical Structure| 61424-26-8

Structure of 3-Benzylaniline
CAS No.: 61424-26-8

Chemical Structure| 61424-26-8

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Product Details of [ 61424-26-8 ]

CAS No. :61424-26-8
Formula : C13H13N
M.W : 183.25
SMILES Code : NC1=CC(CC2=CC=CC=C2)=CC=C1
MDL No. :MFCD01310782

Safety of [ 61424-26-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H228-H315-H319-H335
Precautionary Statements:P210-P261-P305+P351+P338
Class:4.1
UN#:1325
Packing Group:

Application In Synthesis of [ 61424-26-8 ]

* 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 [ 61424-26-8 ]

[ 61424-26-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1171919-75-7 ]
  • [ 61424-26-8 ]
  • tert-butyl (3R)-3-[(2-sulfanylacetyl)amino]piperidine-1-carboxylate [ No CAS ]
  • [ 530-62-1 ]
  • (R)-tert-butyl 3-(5-(3-benzylphenyl)-4-oxo-4,5-dihydro-3H-1-thia-3,5,8-triazaacenaphthylene-2-carboxamido)piperidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
54.5% To a 2-5 mL Biotage microwave vial with a stir bar were added 3-benzylaniline (71.8 mg, 0.384 mmol), 2-chloro-4- iodonicotinonitrile (102 mg, 0.384 mmol), Pd(OAc)2(1.8 mg, 0.0080 mmol), DPEPhos (6.6 mg, 0.012 mmol), and CS2CO3 (173 mg, 0.531 mmol). The vial was sealed, treated with dioxane (0.77 mL), evacuated and flushed with argon 4X, and stirred at 150 C under argon for 30 min. The reaction was cooled to room temperature and was treated with fert-butyl (3R)-3-[(2- sulfany lacetyl)amino]piperi dine- 1 -carboxylate (Intermediate 22) (0.49 M in dioxane, 0.79 mL, 0.39 mmol) via syringe. The vial was sealed and evacuated and flushed with argon 4X, and stirred at 150 C for 15 min. The reaction was then cooled to room temperature, treated with solid CDI (252 mg, 1.55 mmol) in one portion under air, resealed and evacuated and flushed with argon 4X, and stirred at 150 C for 15 min. The reaction was diluted with EtOAc (10 mL), and washed with 0.5 M citric acid and brine (2 x 8 mL) and 2 M K2CO3(1 x 5 mL). The organic phase was dried over anhydrous Na2SC>4, filtered, and concentrated to dryness. The residue was purified by normal phase flash column chromatography (Si02) to give the title compound as a light-beige solid (122 mg, 54.5% yield).
54.5% To a 2-5 mL Biotage microwave vial with a stir bar were added 3-benzylaniline (71.8 mg, 0.384 mmol) , <strong>[1171919-75-7]2-chloro-4-iodonicotinonitrile</strong> (102 mg, 0.384 mmol) , Pd (OAc)2(1.8 mg, 0.0080 mmol) , DPEPhos (6.6 mg, 0.012 mmol) , and Cs2CO3(173 mg, 0.531 mmol) . The vial was sealed, treated with dioxane (0.77 mL) , evacuated and flushed with argon 4X, and stirred at 150 under argon for 30 min. The reaction was cooled to room temperature and was treated with tert-butyl (3R) -3- [ (2- sulfanylacetyl) amino] piperidine-1-carboxylate (Intermediate 22) (0.49 M in dioxane, 0.79 mL, 0.39 mmol) via syringe. The vial was sealed and evacuated and flushed with argon 4X, and stirred at 150 for 15 min. The reaction was then cooled to room temperature, treated with solid CDI (252 mg, 1.55 mmol) in one portion under air, resealed and evacuated and flushed with argon 4X, and stirred at 150 for 15 min. The reaction was diluted with EtOAc (10 mL) , and washed with 0.5 M citric acid and brine (2 x 8 mL) and 2 M K2CO3(1 x 5 mL) . The organic phase was dried over anhydrous Na2SO4, filtered, and concentrated to dryness. The residue was purified by normal phase flash column chromatography (SiO2) to give the title compound as a light-beige solid (122 mg, 54.5yield) .
 

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