Hydrochloric Acid → HCID 67717390, compound
Reaction equation
[NH2:1][CH2:2][CH:3]([C:5]1[CH:6]=[C:7]([CH:12]=[CH:13][C:14]=1[NH:15][S:16]([CH3:19])(=[O:18])=[O:17])[C:8]([O:10]C)=[O:9])[OH:4].[OH-].[Na+].Cl>>[OH2:4].[NH2:1][CH2:2][CH:3]([C:5]1[CH:6]=[C:7]([CH:12]=[CH:13][C:14]=1[NH:15][S:16]([CH3:19])(=[O:18])=[O:17])[C:8]([OH:10])=[O:9])[OH:4]Participants
4
Procedure
A mixture of methyl 3-[2-amino-1-(R,S)-hydroxyethyl]-4-[(methylsulfonyl)amino]benzoate (50 mg, 0.17 mmol) in 1N sodium hydroxide (44 μL, 0.44 mmol) was stirred at room temperature for 4 h. The mixture was neutralized with dilute hydrochloric acid and let stand overnight at room temperature. A white precipitate accumulated which was collected by filtration, washed with water, and dried to give 38 mg (81%) of the title compound as a white powder, mp 274°-276° C.
Workup
- waitlet stand overnight at room temperature
- filtrationwas collected by filtration
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-d72a6b4484bd4709b22a03227f8cec77
- Source dataset
- uspto-grants-1997_02
- Patent number
- US05602277
Reaction notes
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