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Chemical Structure| 1273585-10-6 Chemical Structure| 1273585-10-6

Structure of 1273585-10-6

Chemical Structure| 1273585-10-6

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Product Details of [ 1273585-10-6 ]

CAS No. :1273585-10-6
Formula : C7H2ClFN2O2
M.W : 200.55
SMILES Code : N#CC1=CC(F)=C([N+]([O-])=O)C(Cl)=C1
InChI Key :PNMZVEHEOIYSLE-UHFFFAOYSA-N
Pubchem ID :71116132

Safety of [ 1273585-10-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 1273585-10-6 ]

* 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 [ 1273585-10-6 ]

[ 1273585-10-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1147558-43-7 ]
  • [ 1273585-10-6 ]
YieldReaction ConditionsOperation in experiment
81% With sodium perborate tetrahydrate; acetic acid; In water; acetic acid; at 20 - 80℃; for 73.0h; [0146] Sodium perborate tetrahydrate (131 g, 851 mmol) in acetic acid (200 mL) was heated to 60 C. A solution of<strong>[1147558-43-7]4-amino-3-chloro-5-fluorobenzonitrile</strong> (29.0 g, 170 mmol) in acetic acid (500 mL) was added dropwise, and the resultingreaction was stirred at 60C for 18 h. LCMS analysis indicated -50 % conversion. Additional sodium perborate tetrahydrate(14.4 g, 93.6 mmol) was added, and the reaction was stirred at 70C for 2 h followed by another addition of sodiumperborate tetrahydrate (70.0 g, 455 mmol). The reaction was stirred at 80 C for 5 h and then at rt for 2 d. The reactionwas poured into ice water, and the product was extracted into EtOAc. The combined organics were washed with waterand brine. Finally, the organics were dried over MgSO4, filtered, and concentrated to half volume. Addition of waterresulted in precipitation of the desired product which was collected in a frit, washed with water, and dried in vacuo toprovide an orange solid (27.5 g, 81 % crude yield). 1H NMR (400 MHz, CDCl3) delta 7.68 (s, 1H), 7.55 (d, 1 H).
With sodium perborate; acetic acid; at 20 - 80℃; for 71.0h; 3-Chloro-5-fluoro-4-nitrobenzonitrile Sodium perborate tetrahydrate (131 g, 851 mmol) in acetic acid (200 mL) was heated to 60 C. A solution of <strong>[1147558-43-7]4-amino-3-chloro-5-fluorobenzonitrile</strong> (29.02 g, 170 mmol) in acetic acid (500 ml.) was added dropwise and the reaction was stirred at 60 C for 16 h. The LCMS the indicated the reaction showed -50% conversion. Additional sodium perborate tetrahydrate (14.4 g) was added and the reaction stirred at 70 C for 2 h. Then additional sodium perborate tetrahydrate (70 g) was added and the reaction was stirred at 80 C for 5 h, followed by RT for 2 days. The reaction was then poured into ice water and extracted with EtOAc (3x). The combined organic extracts were washed with H20 (2x), brine, dried over MgS04 and concentrated. When most of the acetic acid was evaporated, water was added to the residue. The orange precipitate was collected by filtration, washed with H20 and air dried to give the crude product as an orange solid. NMR showed the product contaminated with -10% of starting material. This product was used without any further purification.
With sodium perborate tetrahydrate; acetic acid; at 20 - 80℃; for 71.0h; 3-Chloro-5-fluoro-4-nitrobenzonitrileSodium perborate tetrahydrate (131 g, 851 mmol) in acetic acid (200 mL) was heated to 60 C. A solution of <strong>[1147558-43-7]4-amino-3-chloro-5-fluorobenzonitrile</strong> (29.02 g, 170 mmol) in acetic acid (500 mL) was added dropwise and the reaction was stirred at 60 C for 16 h. The LCMS the indicated the reaction showed -50% conversion. Additional sodium perborate tetrahydrate (14.4 g) was added and the reaction stirred at 70 C for 2 h. Then additional sodium perborate tetrahydrate (70 g) was added and the reaction was stirred at 80 C for 5 h, followed by RT for 2 days. The reaction was then poured into ice water and extracted with EtOAc (3x). The combined organic extracts were washed with H20 (2x), brine, dried over MgS04 and concentrated. When most of the acetic acid was evaporated, water was added to the residue. The orange precipitate was collected by filtration, washed with H20 and air dried to give the crude product as an orange solid. NMR showed the product contaminated with -10% of starting material. This product was used without any further purification. 4-Chloro-1-r(3S,5S)-1-oxaspiror2.5loct-5-ylmethyll-1 H-benzimidazole-6-carbonitrile
 

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