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Chemical Structure| 219715-41-0 Chemical Structure| 219715-41-0

Structure of 219715-41-0

Chemical Structure| 219715-41-0

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Product Details of [ 219715-41-0 ]

CAS No. :219715-41-0
Formula : C7H5ClF3NO3S
M.W : 275.63
SMILES Code : O=S(C1=C(C(F)(F)F)C=CN=C1OC)(Cl)=O

Safety of [ 219715-41-0 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H314-H290
Precautionary Statements:P501-P260-P234-P264-P280-P390-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P406-P405
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 219715-41-0 ]

* 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 [ 219715-41-0 ]

[ 219715-41-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 13223-43-3 ]
  • [ 219715-41-0 ]
  • [ 422556-08-9 ]
YieldReaction ConditionsOperation in experiment
94% 2-Amino-5,7-dimethoxy [1,2,4] triazolo [1,5-a] pyrimidine (25.4g, 0.13mol) Add to 137g of dichloromethane, After stirring, 4-dimethylaminopyridine (0.006 g, 0.05 mmol) and 2-methoxy-4-(trifluoromethyl)-pyridine-3-sulfonyl chloride (27.5 g, 0.1 mol), After stirring for 30 minutes, Triethylamine (13.1 g, 0.13 mol) was added dropwise at room temperature. Finally, the temperature was raised to 35 C for 3 h. The mixture was then treated with 4N HCl (60g), was stirred at 25 1 hour, cooled to 10 , filtered, washed with water, washed with methanol and dried to give 40.8 g of pyroxsulam, 94% yield, 98.5% purity (HPLC).
82 - 84% With 3,5-Lutidine; dimethyl sulfoxide; In acetonitrile; at 20℃; for 12h;Product distribution / selectivity; Example 5 Preparation of N-(5,7-dimethoxy[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonamide 2-Amino-5,7-dimethoxy[1,2,4]triazolo[1,5-a]pyrimidine (59 g, 0.30 mol) was combined with 2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonyl chloride (86 g, 0.31 mol, 1.03 eq) in acetonitrile (210 mL) and 3,5-lutidine (120 g, 93% technical). DMSO (1.3 g, 0.017 mol) was added, and the mixture was stirred at room temperature for 12 hours. The mixture was then treated with 4 N HCl (310 mL), after which the mixture was stirred for another 2 hours at 25 C., then cooled to 10 C. The solids were collected by filtration, washed with a 2:1 v/v solution of water:acetonitrile (160 mL), washed with 95% ethanol (2*80 mL), and dried under vacuum at 100 C. to afford 112 g of product assaying at 98 wt % (84% yield from amine, 82% yield from sulfonyl chloride).
78% With 3,5-Lutidine;N-(5,7-dimethoxy[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-S,S-dimethyl-sulfilimine hydrochloride salt; In acetonitrile; at 20℃; for 22h;Product distribution / selectivity; Example 4 Preparation of N-(5,7-dimethoxy[1 2,4]triazolo[1,5-a]pyrimidin-2-yl)-2-methoxy-4-(trifluoromethyl)pyridine-3-sulfonamide 2-Amino-5,7-dimethoxy[1,2,4]triazolo[1,5-a]pyrimidine (9.8 g, 0.050 mol) and N-(5,7-dimethoxy[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)-S,S-dimethyl-sulfilimine hydrochloride salt (1.5 g, 0.005 mol) solids were combined with 2-methoxy-4-(trifluoromethyl)-pyridine-3-sulfonyl chloride (14 g, 0.051 mol) in acetonitrile (40 mL). 3,5-Lutidine (31 g, 93% technical) was added, and the mixture was stirred at room temperature for 22 hours. The mixture was warmed to 42 C. and treated with 3 N HCl (65 mL), after which the mixture was allowed to cool to room temperature over 1.5 hours. The solids were collected by filtration, washed with a 2:1 v/v solution of water:acetonitrile (20 mL), and dried under vacuum at 60 C. to afford 18 g of product assaying at 94 wt % (78% yield).
 

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