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Chemical Structure| 64197-03-1 Chemical Structure| 64197-03-1

Structure of 64197-03-1

Chemical Structure| 64197-03-1

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Product Details of [ 64197-03-1 ]

CAS No. :64197-03-1
Formula : C6H3ClFNO
M.W : 159.55
SMILES Code : O=C(Cl)C1=CC=CC(F)=N1
MDL No. :MFCD04038711

Safety of [ 64197-03-1 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314-H315-H319-H335
Precautionary Statements:P233-P260-P261-P264-P271-P280-P301+P330+P331-P302+P352-P303+P361+P353-P304-P304+P340-P305+P351+P338-P310-P312-P321-P332+P313-P337+P313-P340-P362-P363-P403-P403+P233-P405-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 64197-03-1 ]

* 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 [ 64197-03-1 ]

[ 64197-03-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 402-69-7 ]
  • [ 64197-03-1 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; for 3h;Heating / reflux; Intermediate 20 (1g, 7.09 [MMOL)] was added portionwise to thionyl chloride (3 ml) and the mixture was heated under reflux for 3 hours and then concentrated under reduced pressure. Isopropanol (3 ml) was added to the residue and the mixture was stirred at room temperature for 5 minutes and then concentrated under reduced pressure. The residue was treated with a saturated solution of NaHCO3, extracted with ethyl acetate, the organic phase was dried over [NA2SO4] and concentrated under reduced pressure. The title compound was obtained as an cream oil (1.2g, 93percent); [[APCI] MS] m/z: 184 (MH+).
With thionyl chloride; for 5h;Reflux; 2-fluoro-pyridine-6-carboxylic acid in thionyl chloride (2ml) (86mg, 0.448mmol) was heated under reflux for 5 hours stirred suspension of. Then excess reagent was removed under reduced pressure to give a crude solid. The crude solid, 4- (6-methyl-imidazo [1,2-a] pyridin-2-yl) aniline (100 mg, 0.448 mmol) and dry THF (20 ml) and diisopropylethylamine (94mul, 0.539mmol) in the amide prepared as described in the section amide coupling using, work-up and flash chromatography: the (2 1 EtOAc / hexanes) after to give the title compound 85 mg, 55percent) of a colorless solid .
  • 2
  • [ 79-37-8 ]
  • [ 402-69-7 ]
  • [ 64197-03-1 ]
YieldReaction ConditionsOperation in experiment
97% N,N-dimethyl-formamide; In dichloromethane; at 20℃; for 24h; Oxalyl chloride (1.35 g, 10.6 mmol) was added to a stirred solution of <strong>[402-69-7]6-fluoropicolinic acid</strong> (1.0 g, 7.09 mmol) in CH2Cl2 (25 mL) at rt under argon atmosphere. A drop of DMF was added to initiate reaction. After stirring for 24 h at rt, the solvents were removed in vacuo to yield the acid chloride as a colorless solid (1.35 g, 97percent).
 

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