Hydrochloric Acid → HCID 53897224, compound
Reaction equation
C([O:3][C:4]([C:6]1[O:7][C:8]2[C:16]([NH:17][C:18](=[O:32])[CH:19]=[CH:20][C:21]3[CH:26]=[CH:25][C:24]([CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])=[CH:23][CH:22]=3)=[CH:15][CH:14]=[CH:13][C:9]=2[C:10](=[O:12])[CH:11]=1)=[O:5])C.C(O)C.C(=O)(O)[O-].[Na+].Cl>O>[CH2:27]([C:24]1[CH:23]=[CH:22][C:21]([CH:20]=[CH:19][C:18]([NH:17][C:16]2[C:8]3[O:7][C:6]([C:4]([OH:5])=[O:3])=[CH:11][C:10](=[O:12])[C:9]=3[CH:13]=[CH:14][CH:15]=2)=[O:32])=[CH:26][CH:25]=1)[CH2:28][CH2:29][CH2:30][CH3:31]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
8-(p-pentylcinnamoyl)amino-4-oxo-4H-1-benzopyran-2-carboxylic acid ethyl ester (132 mg; synthesized in example 3) was dissolved into ethanol (10 ml). To the solution, an aqueous solution (1 ml) of sodium bicarbonate (126 mg) was added. The mixture was refluxed for 15 min. To the reaction solution mixture cooled to room temperature, water (20 ml) and 1N hydrochloric acid (2 ml) were added. The mixture was extracted with ethyl acetate. The extract was washed with water and a saturated aqueous solution of sodium chloride, dried, and concentrated under reduced pressure. The residue was washed with a mixture of ethyl acetate and hexane (1:1), and dried to give the title compound (62 mg) having the following physical data:
Workup
- temperatureThe mixture was refluxed for 15 min
- extractionThe mixture was extracted with ethyl acetate
- washThe extract was washed with water
- dry with materiala saturated aqueous solution of sodium chloride, dried
- concentrationconcentrated under reduced pressure
- washThe residue was washed with a mixture of ethyl acetate and hexane (1:1)
- customdried
Sources & evidence
- ORD record
- ord-dcada862b1e449c399c418f73212761d
- Source dataset
- uspto-grants-1988_10
- Patent number
- US04780469
Reaction notes
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