Isopropyl isocyanate → HCID 86686959, compound
Reaction equation
[CH:1]([N:4]=[C:5]=[O:6])([CH3:3])[CH3:2].[F:7][C:8]1[CH:9]=[CH:10][C:11]([NH:14][NH2:15])=[N:12][CH:13]=1>C(Cl)Cl>[F:7][C:8]1[CH:9]=[CH:10][C:11]([NH:14][NH:15][C:5]([NH:4][CH:1]([CH3:3])[CH3:2])=[O:6])=[N:12][CH:13]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Isopropyl isocyanate (0.25 mL, 2.60 mmol) was added dropwise, over 2 min, to a solution of 5-fluoro-2-hydrazinyl-pyridine (for reference procedure see WO 2010/022076, which is incorporated herein by reference in its entirety; 0.30 g, 2.36 mmol) in dry DCM (10 mL) at RT and stirred for 3 h. The solvent was evaporated and the residue triturated (diethyl ether) and filtered to give the title compound as a colourless solid (464 mg, 93%). LCMS (Method 1): Rt 1.92 min, m/z 213 [MH+].
Workup
- customThe solvent was evaporated
- customthe residue triturated (diethyl ether)
- filtrationfiltered
Sources & evidence
- ORD record
- ord-9881a1987c6f499f8696118473f81b87
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08907094B2
Reaction notes
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