Trifluoroacetic acid → HCID 18947042, compound
Reaction equation
[CH3:1][CH:2]([C:4]1[S:5][CH:6]=[C:7]2[CH2:11][N:10](C(OC(C)(C)C)=O)[CH2:9][C:8]=12)[CH3:3].[F:19][C:20]([F:25])([F:24])[C:21]([OH:23])=[O:22]>>[F:19][C:20]([F:25])([F:24])[C:21]([OH:23])=[O:22].[CH3:3][CH:2]([C:4]1[S:5][CH:6]=[C:7]2[CH2:11][NH:10][CH2:9][C:8]=12)[CH3:1]Participants
3
Procedure
A solution of 0.49 g (1.8 mmol) of 1-(1-methylethyl)5-(1,1-dimethylethoxy)carbonyl-5,6-dihydro -4H-thieno[3,4-c]pyrrole in 0.5 ml of trifluoroacetic acid is stirred for 30 min at a temperature in the region of 20° C. After evaporation of the solvent, 0.51 g of an oily product is obtained. Quantitative yield.
Workup
- customAfter evaporation of the solvent
Sources & evidence
- ORD record
- ord-53f02e5540364c7a80628e67b63888f6
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05380742
Reaction notes
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