Sodium Hydroxide → HCID 67007765, compound
Reaction equation
C[O:2][C:3]([C:5]1[S:6][C:7]([CH2:10][CH2:11][N:12]2[CH:17]=[CH:16][C:15]([O:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)=[CH:14][C:13]2=[O:26])=[CH:8][CH:9]=1)=[O:4].[OH-].[Na+]>CO>[CH2:19]([O:18][C:15]1[CH:16]=[CH:17][N:12]([CH2:11][CH2:10][C:7]2[S:6][C:5]([C:3]([OH:4])=[O:2])=[CH:9][CH:8]=2)[C:13](=[O:26])[CH:14]=1)[C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To 540 mg (1.46 mmol) 5-[2-(4-benzyloxy-2-oxo-2H-pyridin-1-yl)-ethyl]-thiophene-2-carboxylic acid methyl ester (preparation 11b) in 8.0 mL MeOH is added 5.5 mL (5.50 mmol) 1M aqueous sodium hydroxide-solution. The reaction is stirred overnight at RT and additional 3.0 mL (3.00 mmol) 1M aqueous sodium hydroxide-solution is added. The reaction mixture is stirred 4 days at RT and the solvent is evaporated. The residue is acidified with 1M aqueous HCl, the precipitate is collected, washed with water and dried.
Workup
- stirringThe reaction mixture is stirred 4 days at RT
- customthe solvent is evaporated
- customthe precipitate is collected
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-c4d9f2362919411cae91d7b785e4a14f
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08067590B2
Reaction notes
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