Hydrochloric Acid → HCID 66611962, compound
Reaction equation
[CH3:1][N:2]([CH3:35])[C:3]([C:5]1[C:20]([C:21]2[CH:22]=[N:23][N:24]([CH3:26])[CH:25]=2)=[CH:19][C:8]([C:9]([O:11]CC2C=CC=CC=2)=[O:10])=[C:7]([O:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH:6]=1)=[O:4].[OH-].[Li+].O.Cl>O1CCCC1>[CH3:1][N:2]([CH3:35])[C:3]([C:5]1[C:20]([C:21]2[CH:22]=[N:23][N:24]([CH3:26])[CH:25]=2)=[CH:19][C:8]([C:9]([OH:11])=[O:10])=[C:7]([O:27][CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH:6]=1)=[O:4]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of phenylmethyl 4-[(dimethylamino)carbonyl]-5-(1-methyl-1H-pyrazol-4-yl)-2-[(phenylmethyl)oxy]benzoate (may be prepared as described in Description 40; 195 mg, 0.42 mmol) in tetrahydrofuran (4 ml) was added lithium hydroxide (34 mg, 1.42 mmol) and water (1 ml). The mixture was for 18 hours then 2M hydrochloric acid (0.73 ml, 1.45 mmol) was added. The solvent removed in vacuo to give the title compound as a gum. 154 mg.
Workup
- customThe solvent removed in vacuo
Sources & evidence
- ORD record
- ord-cfd89df397f44e278fef1b341f543b75
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09365551B2
Reaction notes
Loading…