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2-Naphthoyl chloride → HCID 10083909, compound

HRID 1199372
Notes
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Reaction equation

HRID 1199372 reaction equation
[CH3:1][NH:2][C:3](=[S:6])[NH:4][NH2:5].[CH:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=[CH:9][C:8]=1[C:17](Cl)=[O:18]>N1C=CC=CC=1>[CH3:1][NH:2][C:3](=[S:6])[NH:4][NH:5][C:17]([C:8]1[CH:9]=[CH:10][C:11]2[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=2)[CH:7]=1)=[O:18]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 752462-Naphthoyl chlorideHCID 2723853N-Methylhydrazinecarbothioamide

Product 1

HCID 10083909HCID 10083909, compound

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

To a stirred room temperature solution of 4-methylthiosemicarbazide (5.91 g, 5.62×10-2 mole) and pyridine (150 ml) was added 2-naphthoyl chloride (10.7 g, 5.61×10-2 mole). After stirring overnight, the pyridine was evaporated at reduced pressure. The concentrate was treated with water and the undissolved product was collected by filtration and dried by suction.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • customthe pyridine was evaporated at reduced pressure
  • additionThe concentrate was treated with water
  • filtrationthe undissolved product was collected by filtration
  • customdried by suction
  • Sources & evidence

    ORD record
    ord-c9281fd746634014bc2368dea7eb7761
    Source dataset
    uspto-grants-1990_02
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04900743

    Reaction notes

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