Potassium Hydroxide → HCID 58011657, compound
Reaction equation
C([O:3][C:4](=[O:23])[CH2:5][N:6]1[C:10](=[O:11])[N:9]([CH:12]2[CH2:14][CH2:13]2)[C:8]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[O:21][CH3:22])=[N:7]1)C.[OH-].[K+]>CO>[CH:12]1([N:9]2[C:10](=[O:11])[N:6]([CH2:5][C:4]([OH:23])=[O:3])[N:7]=[C:8]2[C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[O:21][CH3:22])[CH2:14][CH2:13]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
140 mg (0.44 mmol) of ethyl[4-cyclopropyl-3-(2-methoxyphenyl)-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl]-acetate from Example 72A are placed in 0.3 ml methanol and stirred overnight at room temperature with 0.12 ml of 20% aqueous potassium hydroxide. This is then concentrated and adjusted to about pH 1 with 1 N hydrochloric acid. The precipitated solid is filtered off, washed with diethyl ether and then dried in vacuo. 81 mg (63% of theory) of the target compound are thus obtained.
Workup
- concentrationThis is then concentrated
- filtrationThe precipitated solid is filtered off
- washwashed with diethyl ether
- customdried in vacuo
- custom81 mg (63% of theory) of the target compound are thus obtained
Sources & evidence
- ORD record
- ord-c91e3990558145cc8f9f34b1b584536f
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08084481B2
Reaction notes
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