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Chemical Structure| 1007874-87-4 Chemical Structure| 1007874-87-4

Structure of 1007874-87-4

Chemical Structure| 1007874-87-4

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Product Details of [ 1007874-87-4 ]

CAS No. :1007874-87-4
Formula : C7H3F3N2O2S
M.W : 236.17
SMILES Code : O=C(C1=C(C(F)(F)F)N=C2SC=CN21)O
MDL No. :MFCD11889976

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Application In Synthesis of [ 1007874-87-4 ]

* 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 [ 1007874-87-4 ]

[ 1007874-87-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 564443-27-2 ]
  • [ 1007874-87-4 ]
YieldReaction ConditionsOperation in experiment
55% With sodium chlorite; sodium dihydrogenphosphate dihydrate; In water; tert-butyl alcohol; at 20℃; A solution of sodium chlorite 418.986 mg (4.633 mmol) and sodium dihydrogen phosphate dihydrate 553.971 mg (3.551 mmol) in water 3.94 mL (218.895 mmol) was added dropwise to a solution of <strong>[564443-27-2]6-trifluoromethyl-imidazo[2,1-b]thiazole-5-carbaldehyde</strong> 119 mg (0.54 mmol) in t-BuOH (3.94 mL). The mixture was stirred for 2 h30 at RT. The mixture was then concentrated in vacuo to remove t-BuOH, a white precipitate was formed and filtered to give the title compound as a white solid (70 mg, 55%).LC-MS: rt=0.74 min, 278 [M+H+MeCN]+.
With sodium chlorite; sodium dihydrogenphosphate; In water; tert-butyl alcohol; at 20℃; for 1.5h;Heating / reflux; At 00C POCl3 (17.1 mmol) is added dropwise to a solution of DMF (20.6 mmol) in chloroform (5.0 mL). A solution of 6-trifluoromethyl-imidazo[2,l-b]thiazole (3.17 mmol) in chloroform (15 mL) is added dropwise at 00C and the mixture is stirred for 3h at RT. After heating for 2.5d to reflux the mixture is poured into ice, extracted three times with DCM, dried over MgSO4 and concentrated under reduced pressure. DCM is added, the obtained precipitate is filtered off and the filtrate is concentrated in vacuo to give a crude product which is dissolved in tert.-butanol (19.5 mL). A solution of sodium chlorite (23.0 mmol) and NaH2PO4 (17.6 mmol) in water (19.5 mL) is added dropwise and the mixture is stirred for 90 min at RT. The solvents are partially removed in vacuo and the obtained precipitate is filtered off to give the desired product as a white solid. LC-MS: tR = 0.73 min; [M+H]+ = 237.2.
With sodium chlorite; sodium dihydrogenphosphate; water; In tert-butyl alcohol; at 20℃; for 1.5h; At 00C POCl3 (17.1 mmol) is added dropwise to a solution of DMF (20.6 mmol) in chloroform (5.0 mL). A solution of 6-trifluoromethyl-imidazo[2,l-b]thiazole (3.17 mmol) in chloroform (15 mL) is added dropwise at 00C and the mixture is stirred for 3h at RT. After heating for 2.5d to reflux the mixture is poured into ice, extracted three times with DCM, dried over MgSO4 and concentrated under reduced pressure. DCM is added, the obtained precipitate is filtered off and the filtrate is concentrated in vacuo to give a crude product which is dissolved in tert.-butanol (19.5 mL). A solution of sodium chlorite (23.0 mmol) and sodium dihydrogen phosphate dihydrate (17.6 mmol) in water (19.5 mL) is added dropwise and the mixture is stirred for 90 min at RT. The solvents are partially removed in vacuo and the obtained precipitate is filtered off to give the desired product as a white solid. LC-MS: tR = 0.73 min; [M+H]+ = 237.2.
 

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