Hydrochloric Acid → HCID 66612080, compound
Reaction equation
[CH3:1][N:2]1[CH:6]=[C:5]([C:7]2[C:8]([C:31]([N:33]3[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]3)=[O:32])=[CH:9][C:10]([O:23][CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)=[C:11]([CH:22]=2)[C:12]([O:14]CC2C=CC=CC=2)=[O:13])[CH:4]=[N:3]1.[OH-].[Li+].O.Cl>O1CCCC1>[CH3:1][N:2]1[CH:6]=[C:5]([C:7]2[C:8]([C:31]([N:33]3[CH2:38][CH2:37][CH2:36][CH2:35][CH2:34]3)=[O:32])=[CH:9][C:10]([O:23][CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)=[C:11]([CH:22]=2)[C:12]([OH:14])=[O:13])[CH:4]=[N:3]1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of phenylmethyl 5-(1-methyl-1H-pyrazol-4-yl)-2-[(phenylmethyl)oxy]-4-(1-piperidinylcarbonyl)benzoate (may be prepared as described in Description 37; 194 mg, 0.38 mmol) in tetrahydrofuran (4 ml) was added lithium hydroxide (33 mg, 1.38 mmol) and water (1 ml). The solution was stirred for 18 hours then 2M hydrochloric acid (0.69 ml, 1.38 mmol) was added and the solvent removed in vacuo to give the title compound as a gum. 170 mg.
Workup
- customthe solvent removed in vacuo
Sources & evidence
- ORD record
- ord-ee14ce4595f8466dbf333d49b8665800
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09365551B2
Reaction notes
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