Methyl isothiocyanate → HCID 86759511, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][CH:16]=1)[C:5]([CH:7]1[CH2:12][CH2:11][N:10]([CH3:13])[CH2:9][CH2:8]1)=[O:6].[CH3:17][N:18]=[C:19]=[S:20]>>[CH3:17][NH:18][C:19](=[S:20])[NH:1][C:2]1[CH:3]=[C:4]([CH:14]=[CH:15][CH:16]=1)[C:5]([CH:7]1[CH2:8][CH2:9][N:10]([CH3:13])[CH2:11][CH2:12]1)=[O:6]Participants
3
Procedure
Following the example above and beginning with 4-[3-aminobenzoyl]-1-methylpiperidine (25 mg, 0.115 mmol) and methyl isothiocyanate (124 μL, 1.813 mmol), 22.0 mg (66%) of the title compound were recovered.
Sources & evidence
- ORD record
- ord-7da0bee5f7c8475988b2199aa830e197
- Source dataset
- uspto-grants-2004_08
- Patent number
- US06777428B1
Reaction notes
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