Hydrochloric Acid → 4-[2-(Thiazol-2-ylamino)ethyloxy]benzoic acid hydrochloride
Reaction equation
[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[NH:6][CH2:7][CH2:8][O:9][C:10]1[CH:19]=[CH:18][C:13]([C:14]([O:16]C)=[O:15])=[CH:12][CH:11]=1.[ClH:20]>>[ClH:20].[S:1]1[CH:5]=[CH:4][N:3]=[C:2]1[NH:6][CH2:7][CH2:8][O:9][C:10]1[CH:19]=[CH:18][C:13]([C:14]([OH:16])=[O:15])=[CH:12][CH:11]=1Participants
3
Procedure
Ester 24-4 (180 mg, 0.65 mmol) was heated at 50° in 6 mL 6 N HCl for 16 h, then concentrated providing 24-5 as a yellow solid.
Workup
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-d438a0e7dfce452d857d5b046eab21aa
- Source dataset
- uspto-grants-1998_04
- Patent number
- US05741796
Reaction notes
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