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Chemical Structure| 19731-01-2 Chemical Structure| 19731-01-2

Structure of 19731-01-2

Chemical Structure| 19731-01-2

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Product Details of [ 19731-01-2 ]

CAS No. :19731-01-2
Formula : C8H7N3O
M.W : 161.16
SMILES Code : NNC(=O)C1=CC(=CC=C1)C#N
MDL No. :MFCD09802347
InChI Key :KYKPMNVLZRQRHZ-UHFFFAOYSA-N
Pubchem ID :21942658

Safety of [ 19731-01-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 19731-01-2 ]

* 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 [ 19731-01-2 ]

[ 19731-01-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 13531-48-1 ]
  • [ 19731-01-2 ]
YieldReaction ConditionsOperation in experiment
With hydrazine hydrate; In methanol; for 5h;Reflux; General procedure: Compounds 6a-t were synthesized from substituted benzoic acid via six steps according to the literature method as described. Various substituted benzoic acids 1a-t were treated with SOCl2 to give compounds 2a-t, which were reacted with CH3OH and EtN3 in CH2Cl2 at 0 to afford compounds 3a-t. Compounds 4a-t were prepared by the reaction of compounds 3a-t, hydrazine hydrate in CH3OH under reflux condition about 5h. Subsequently, compounds 5a-t were obtained by reaction of compounds 4a-t with CS2 and KOH in CH3OH. Compounds 6a-t were obtained by the cyclization reaction of compounds 5a-t in the presence of HCl at 0-5°C.
3.200 g With hydrazine hydrate; In methanol; at 0 - 20℃; for 16h; To a stirred solution of <strong>[13531-48-1]methyl 3-cyanobenzoate</strong> (CAS Number 1353 1-48-1; 4.000 g, 24.84 mmol) in MeOH (40 ml) was added hydrazine hydrate (3.1 ml, 62.0 mmol) at 0°C. The reaction mixture was stirred at rt for 16 h. The resulting reaction mixture was concentrated under vacuum, diluted with water (200 ml) and extracted with DCM (2 x 200 ml). The combined organic layer wasdried over Na2SO4, filtered and concentrated under reduced pressure. The resulting residue was purified by flash column chromatography (70percent EtOAc in hexane) yielding 3-cyanobenzohydrazide (3.200 g, 19.87 mmol). LCMS: Method C, 0.934 mi MS: ES+ 162.36; ?H NMR (400 MHz, DMSOd 6) ppm 9.99 (s, 1 H), 8.21 (s, 1 H), 8.13 (d, J = 7.6 Hz, 1 H), 8.00 (d, J = 7.6 Hz, 1 H), 7.69 (t, J = 8.0 Hz, 1 H), 4.58 (s, 2 H).
 

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