Reaction equation
C([O:3][C:4]([C:6]1([NH:15][C:16]([C:18]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[CH:21]=[CH:20][C:19]=2[O:28][CH2:29][CH3:30])=[O:17])[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7]1)=[O:5])C.[OH-].[K+].O>CCO>[CH2:29]([O:28][C:19]1[CH:20]=[CH:21][C:22]2[C:27](=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:18]=1[C:16]([NH:15][C:6]1([C:4]([OH:5])=[O:3])[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7]1)=[O:17])[CH3:30]Participants
5
Procedure
The mixture of 2-[(2-ethoxy-naphthalene-1-carbonyl)-amino]-indan-2-carboxylic acid ethyl ester (45) (270 mg, 0.67 mmol) and KOH (600 mg, 10.7 mmol) is dissolved in EtOH (10 mL) and water (1 mL) under a water bath. The water bath is removed when KOH is completely dissolved and the resulting reaction solution is stirred at RT for 8 h. After concentration in vacuo, the residue is dissolved in water (20 mL) and acidified with conc. HCl until pH ˜4. The precipitate is filtered to give a pure product (46) as white solid (170 mg, 68%).
Workup
- customThe water bath is removed when KOH
- dissolutionis completely dissolved
- customthe resulting reaction solution
- concentrationAfter concentration in vacuo
- dissolutionthe residue is dissolved in water (20 mL)
- filtrationThe precipitate is filtered
Sources & evidence
- ORD record
- ord-c279cadec9a54f52ba14348f80b6867b
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08569535B2
Linked notes
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