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Chemical Structure| 70010-48-9 Chemical Structure| 70010-48-9

Structure of 70010-48-9

Chemical Structure| 70010-48-9

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Product Details of [ 70010-48-9 ]

CAS No. :70010-48-9
Formula : C10H9NS
M.W : 175.25
SMILES Code : NC1=CC=C(C2=CC=CS2)C=C1
MDL No. :MFCD01224064

Safety of [ 70010-48-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H315-H318-H335
Precautionary Statements:P261-P280-P301+P310-P305+P351+P338
Class:8(6.1)
UN#:2923
Packing Group:

Application In Synthesis of [ 70010-48-9 ]

* 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 [ 70010-48-9 ]

[ 70010-48-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 70010-48-9 ]
  • [ 1171919-75-7 ]
  • tert-butyl (3R)-3-[(2-sulfanylacetyl)amino]piperidine-1-carboxylate [ No CAS ]
  • [ 530-62-1 ]
  • (R)-tert-butyl 3-(4-oxo-5-(4-(thiophen-2-yl)phenyl)-4,5-dihydro-3H-1-thia-3,5,8-triazaacenaphthylene-2-carboxamido)piperidine-1-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
55% To a 2-5 mL Biotage microwave vial with stir bar were added l,l'-bis(diphenylphosphino)ferrocene- palladium(II)dichlorideDCM complex (2.3 mg, 0.0028 mmol), <strong>[1171919-75-7]2-chloro-4-iodonicotinonitrile</strong> (39.9 mg, 0.151 mmol), 4-thiophen-2-ylphenylamine (26.8 mg, 0.153 mmol), and Cs2C03(71 mg, 0.22 mmol) under air at room temperature. The vial was sealed, and 1,4-dioxane (0.3 mL) was added via syringe, and quickly evacuated/flushed with argon 4X. The mixture was stirred at 150 C under argon for 30 min. The reaction was treated with (R)-tert-buty 3-(2- mercaptoacetamido)piperidine-1-carboxylate (Intermediate 22) (0.24 mL, 0.156 mmol) via syringe at room temperature, and stirred under argon at 150 C for 15 min. The amber mixture was then cooled to room temperature, opened, and treated with CDI (102 mg, 0.629 mmol) in one portion under air. The microwave vial was resealed, evacuated/flushed with argon 4X, and stirred at 150 C under argon for 15 min. The reaction was then cooled to room temperature, diluted with EtOAc (10 mL), and washed with 0.5 M citric acid/brine (2 x 5 mL; final pH -1-2) and 2 M K2CO3(1 x 5 mL; final pH >10). The clear amber organic phase was then dried over anhydrous Na2SC>4, filtered, and concentrated to dryness. The residue was dissolved in DCM (0.75 mL) and purified by flash column chromatography to give the title compound as a yellow foam (48 mg, 55%).
55% To a 2-5 mL Biotage microwave vial with stir bar were added 1, 1'-bis (diphenylphosphino) ferrocene-palladium (II) dichloride·DCM complex (2.3 mg, 0.0028 mmol) , <strong>[1171919-75-7]2-chloro-4-iodonicotinonitrile</strong> (39.9 mg, 0.151 mmol) , 4-thiophen-2-ylphenylamine (26.8 mg, 0.153 mmol) , and Cs2CO3(71 mg, 0.22 mmol) under air at room temperature. The vial was sealed, and 1, 4-dioxane (0.3 mL) was added via syringe, and quickly evacuated/flushed with argon 4X. The mixture was stirred at 150 under argon for 30 min. The reaction was treated with (R) -tert-butyl 3- (2-mercaptoacetamido) piperidine-1-carboxylate (Intermediate 22) (0.24 mL, 0.156 mmol) via syringe at room temperature, and stirred under argon at 150 for 15 min. The amber mixture was then cooled to room temperature, opened, and treated with CDI (102 mg, 0.629 mmol) in one portion under air. The microwave vial was resealed, evacuated/flushed with argon 4X, and stirred at 150 under argon for 15 min. The reaction was then cooled to room temperature, diluted with EtOAc (10 mL) , and washed with 0.5 M citric acid/brine (2 x 5 mL final pH 1-2) and 2 M K2CO3(1 x 5 mL final pH >10) . The clear amber organic phase was then dried over anhydrous Na2SO4, filtered, and concentrated to dryness. The residue was dissolved in DCM (0.75 mL) and purified by flash column chromatography to give the title compound as a yellow foam (48 mg, 55) .
 

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