Lithium hydroxide, monohydrate → HCID 66729176, compound
Reaction equation
[C:1]([C:5]1[N:10]=[C:9](C2C=CC=C(F)C=2)[C:8]([C:18]([O-:20])=[O:19])=[CH:7][N:6]=1)([CH3:4])([CH3:3])[CH3:2].O[Li].[OH2:23]>>[C:1]([C:5]1[N:10]=[C:9]([N:6]2[CH2:7][CH2:8][O:23][CH2:1][CH2:5]2)[C:8]([C:18]([OH:20])=[O:19])=[CH:7][N:6]=1)([CH3:2])([CH3:3])[CH3:4]Participants
3
Procedure
Using a procedure to Example B40, 2-tert-butyl-4-(3-fluorophenyl)pyrimidine-5-carboxylate (0.27 g, 0.89 mmol) was treated with LiOH—H2O (86 mg, 3.57 mmol) to afford 2-tert-butyl-4-morpholinopyrimidine-5-carboxylic acid (0.23 g, 92% yield). MS (ESI) m/z: 275.0 (M+H+).
Sources & evidence
- ORD record
- ord-f078888f8e0a4944946a113eca555a54
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08188113B2
Reaction notes
Loading…