Tetrahydro-4H-pyran-4-ol → HCID 68825367, compound
Reaction equation
[OH:1][CH:2]1[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1.Cl[C:9]1[C:18]2[C:13](=[CH:14][CH:15]=[C:16]([I:19])[CH:17]=2)[N:12]=[CH:11][C:10]=1[C:20]#[N:21].[H-].[K+]>C1COCC1>[I:19][C:16]1[CH:17]=[C:18]2[C:13](=[CH:14][CH:15]=1)[N:12]=[CH:11][C:10]([C:20]#[N:21])=[C:9]2[O:1][CH:2]1[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Similar procedure as described in example 28a was used, starting from 4-hydroxy tetrahydropyran, 4-chloro-6-iodo-quinoline-3-carbonitrile (example 14c) and potassium hydride in a solvent system of THF to give 6-iodo-4-(tetrahydro-pyran-4-yloxy)-quinoline-3-carbonitrile. LC-MS m/e 381 (MH+).
Sources & evidence
- ORD record
- ord-9bd07f5308e2466780b2431cd87f537a
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07250515B2
Reaction notes
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