Lawesson's reagent → HCID 86643701, compound
Reaction equation
[I:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([NH:7][NH2:8])=O.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:21])=CC=1>C1(C)C=CC=CC=1>[I:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][CH:11]=1)[C:5]([NH:7][NH2:8])=[S:21]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3-Iodobenzohydrazide (500 mg, 1.91 mmol) obtained in Step 1 of Example 52 was suspended in toluene (10 mL), and the mixture was refluxed for 1 hour after adding Lawesson's reagent (772 mg, 1.91 mmol). The mixture was then purified by silica gel column chromatography to give 3-iodothiobenzohydrazide (391 mg, 74%).
Workup
- temperaturethe mixture was refluxed for 1 hour
- customThe mixture was then purified by silica gel column chromatography
Sources & evidence
- ORD record
- ord-d433ef6b86d44c6db92c2bb892b2bbb0
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07998954B2
Reaction notes
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