3-Hydroxypyridine → HCID 21901945, compound
Reaction equation
[OH:1][C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.C(=O)([O-])[O-].[Cs+].[Cs+].O1C2C=CC(O[CH2:24][CH:25]3[CH2:30][CH2:29][CH2:28][N:27]([C:31]([C:33]4([C:37]5[CH:42]=[CH:41][C:40]([Cl:43])=[CH:39][CH:38]=5)[CH2:36][CH2:35][CH2:34]4)=[O:32])[CH2:26]3)=CC=2OC1>>[Cl:43][C:40]1[CH:41]=[CH:42][C:37]([C:33]2([C:31]([N:27]3[CH2:28][CH2:29][CH2:30][CH:25]([CH2:24][O:1][C:2]4[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=4)[CH2:26]3)=[O:32])[CH2:36][CH2:35][CH2:34]2)=[CH:38][CH:39]=1Participants
4
Procedure
Compound 85 was synthesized from 3-hydroxypyridine (0.25 g, 2.60 mmol), cesium carbonate (1.27 g, 3.89 mmol) and compound 43 (1.0 g, 2.60 mmol), using the method described for the synthesis of compound 44 to give 0.52 g of the desired product 85. C22H25ClN2O2, LRMS (m/z)=385 (MH+).
Sources & evidence
- ORD record
- ord-3007a5c6c84c4381b52d1b4f5c99e12c
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07132551B2
Reaction notes
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