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[ CAS No. 107707-33-5 ] {[proInfo.proName]}

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Chemical Structure| 107707-33-5
Chemical Structure| 107707-33-5
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Product Details of [ 107707-33-5 ]

CAS No. :107707-33-5 MDL No. :MFCD00041168
Formula : C7H6Cl2N2S Boiling Point : No data available
Linear Structure Formula :- InChI Key :BNJARXOEVLYKDN-UHFFFAOYSA-N
M.W : 221.11 Pubchem ID :2737539
Synonyms :

Safety of [ 107707-33-5 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P501-P270-P264-P301+P310+P330-P405 UN#:2811
Hazard Statements:H301 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 107707-33-5 ]

* 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.

  • Upstream synthesis route of [ 107707-33-5 ]
  • Downstream synthetic route of [ 107707-33-5 ]

[ 107707-33-5 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 107707-33-5 ]
  • [ 158465-13-5 ]
YieldReaction ConditionsOperation in experiment
81% With bromine In chloroform at 0 - 60℃; for 10 h; j00330j To a solution of compound B-28 (1.0 g, 3.7 mmol) in chloroform (20 mL) at 0 °C was added bromine (1.2 g, 7.4 mmol). The mixture was stirred at 60 °C for 10 hours, then cooled to room temperature and filtered to collect the solid. The solid was washed with acetone (4 x 5 mL), then added into water (45 mL). The mixture was stirred at 95 °C for 30 mm, then adjusted to pH 9 with sodium hydroxide (0.5 M). The solid was collected by filtration and dried in vacuo to give compound B-29 (0.68 g, 81percent yield) as a purple gray solid. ‘H-NMR (CDC13, 400 MHz): 7.43 (d, J=1.6 Hz, 1H), 7.15 (d, J1.6 Hz, 1H), 5.32 (bs, 2H).
42% With dioxane dibromide In 1,4-dioxane; chloroform at 0 - 80℃; for 23 h; Inert atmosphere In the (3,5-dichlorophenyl) thiourea (5 00mg, 2.26mg)The chloroform solution (4.0 ml), andIn a nitrogen environment at 0 ° CBromo-1,4-dioxane was added fathoms complexCompound (5 61mg, 2.26mol),The 0 ° C was stirred for 1.0 hours at 80 ° C for 22 h.The reaction mixture was cooled, concentrated under reduced pressure and the residue thus obtained was washed with water, recrystallized from ethanol. The powder separated by filtration to obtain it, and the filtrate was concentrated under reduced pressure and the obtained residue was washed with ethanol, collected by filtration to filter powder. Merger of two kinds of powder, to obtain the title compound (209mg, 42percent).
Reference: [1] Patent: WO2017/69980, 2017, A1, . Location in patent: Paragraph 00329; 00330
[2] Farmaco, 1998, vol. 53, # 12, p. 752 - 757
[3] Patent: TW2016/5805, 2016, A, . Location in patent: Paragraph 0372; 0373
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