Acetic Acid → HCID 20381778, compound
Reaction equation
C[O:2][C:3]([C:5]1[NH:6][C:7]2[C:12]([C:13]=1[O:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[NH2:21])=[CH:11][CH:10]=[CH:9][CH:8]=2)=[O:4].O.C(O)(=O)C>C(O)C>[NH2:21][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[O:14][C:13]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[NH:6][C:5]=1[C:3]([OH:4])=[O:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1.6 g of methyl-3-[o-aminophenoxy]-indole-2-carboxylate was dissolved in 10 ml each of ethanol and water and refluxed for 10 min. The clear solution was acidified with acetic acid. The white precipitate was filtered and recrystallized from acetonitrile to give analytical material, mp. 217°-18°.
Workup
- filtrationThe white precipitate was filtered
- customrecrystallized from acetonitrile
- customto give analytical material, mp. 217°-18°
Sources & evidence
- ORD record
- ord-ffc1062fb0af42ffaa9f12094b99ac66
- Source dataset
- uspto-grants-1979_12
- Patent number
- US04179513
Reaction notes
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