Hydrochloric Acid → 2-bromo-4H-thieno[3,2-b]pyrrole-5-carboxylic acid
Reaction equation
C([O:3][C:4]([C:6]1[NH:10][C:9]2[CH:11]=[C:12]([Br:14])[S:13][C:8]=2[CH:7]=1)=[O:5])C.Cl>>[Br:14][C:12]1[S:13][C:8]2[CH:7]=[C:6]([C:4]([OH:5])=[O:3])[NH:10][C:9]=2[CH:11]=1Participants
3
Procedure
2-Bromo-4H-thieno[3,2-b]pyrrole-5-carboxylic acid ethyl ester (Eras, J.; Galvez, C.; Garcia, F., J. Heterocycl. Chem., 21: 215-217 (1984)) was hydrolyzed according to Procedure D (after cooling to room temperature, acidification with 2 N HCl; resultant precipitate filtered, suspended in toluene, concentrated; no purification).
Workup
- filtrationresultant precipitate filtered
- concentrationconcentrated
- customno purification)
Sources & evidence
- ORD record
- ord-fbda73132a89485eb889b72ab2d59aa3
- Source dataset
- uspto-grants-2003_06
- Patent number
- US06576653B2
Reaction notes
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