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[ CAS No. 1416800-51-5 ] {[proInfo.proName]}

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Chemical Structure| 1416800-51-5
Chemical Structure| 1416800-51-5
Structure of 1416800-51-5 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1416800-51-5 ]

CAS No. :1416800-51-5 MDL No. :MFCD30828946
Formula : C10H13BrN2OS Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 289.19 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 1416800-51-5 ]

* 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.

  • Downstream synthetic route of [ 1416800-51-5 ]

[ 1416800-51-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 343338-28-3 ]
  • [ 405174-97-2 ]
  • [ 1416800-51-5 ]
YieldReaction ConditionsOperation in experiment
With copper(II) sulfate; In dichloromethane; at 20℃; Step 3. (S,E)-N-((3-Bromopyridin-2-yl)methylene)-2-methylpropane-2- sulflnamideA mixture of 3-bromo piconaldehyde (10 g, 53.8 mmol), copper sulfate (3.98 mL, 81 mmol) and (5)-2-methylpropane-2-sulfinamide (6.84 g, 56.4 mmol) in DCM (100 mL) was stirred at rt overnight. The solid was filtered off and the filtrate concentrated under vacuum. The residue thus obtained was purified by column chromatography using silica (100-200 mesh) with 20% EtOAc in n- hexane as eluent to give (S,E)-N-((3-bromopyridin-2-yl)methylene)-2- methylpropane-2-sulfinamide as yellow oil. 1H-NMR (400 MHz, CDC13): delta ppm 9.0 (s, 1H), 8.75 (d, 1H), 7.97 (d, 1H), 7.32 (t, 1H), 5.2 (d, 1H), 1.3 (s, 9H).
copper(II) sulfate; In dichloromethane; at 20℃; Step 3. (S,E)-N-((3-Bromopyridin-2-yl)methylene)-2-methylpropane-2- sulflnamideA mixture of 3-bromo piconaldehyde (10 g, 53.8 mmol), copper sulfate (3.98 mL, 81 mmol) and (5)-2-methylpropane-2-sulfinamide (6.84 g, 56.4 mmol) in DCM (100 mL) was stirred at rt overnight. The solid was filtered off and the filtrate concentrated under vacuum. The residue was purified by column chromatography using silica (100-200 mesh) with 20% EtOAc in n-hexane as eluent to give (S,E)-N-((3-bromopyridin-2-yl)methylene)-2-methylpropane-2- sulfinamide as yellow oil. 1H-NMR (400 MHz, CDC13): 9.0(s, 1H), 8.74-8.76(d, 1H), 7.9-8.04(d, 1H), 7.26-7.38(t 1H), 5.2(d, 1H), 1.3(s, 9H).
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