Hydrochloric Acid → HCID 25117629, compound
Reaction equation
[C:1]([CH2:4][CH2:5][C:6]([NH:8][C:9]1[CH:18]=[CH:17][C:12]([C:13](OC)=[O:14])=[C:11]([OH:19])[CH:10]=1)=[O:7])([OH:3])=[O:2].Cl.[OH-].[NH4+:22]>>[C:1]([CH2:4][CH2:5][C:6]([NH:8][C:9]1[CH:18]=[CH:17][C:12]([C:13]([NH2:22])=[O:14])=[C:11]([OH:19])[CH:10]=1)=[O:7])([OH:3])=[O:2]Participants
4
Procedure
Methyl 4-(3-carboxy-propionylamino)-2-hydroxybenzoate (1 g) from Example 2 is dissolved in 5 mL of 28% ammonium hydroxide solution. The reaction mixture is stirred at ambient conditions for 16 hours. In an ice-water bath, the solution is carefully acidified using concentrated hydrochloric acid. The precipitate is collected by filtration, washed with water and dried.
Workup
- customIn an ice-water bath, the solution is carefully acidified using concentrated
- filtrationThe precipitate is collected by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-a6dd87129eb940c1abad1ed13aa1bc99
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08426466B2
Reaction notes
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