Trifluoroacetic acid → HCID 88813774, compound
Reaction equation
[NH:1](C(OC(C)(C)C)=O)[C@H:2]([C:4]([NH:6][CH2:7][C:8]([O:10][CH3:11])=[O:9])=[O:5])[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].[CH3:11][O:10][C:8](=[O:9])[CH2:7][NH:6][C:4](=[O:5])[C@H:2]([CH3:3])[NH2:1]Participants
3
Conditions
- Temperature
- 0 °C
Procedure
Boc-Ala-Gly-OMe [10 g, 45 mmoles, described by H. U. Immer et al., Helv. Chim. Acta, 57, 730 (1974)] is dissolved in cold (ice bath) trifluoroacetic acid (100 ml). The solution is stirred for 1 hr at 0° C and the solvent evaporated. The residue is dissolved in methanol, added to diethyl ether and the precipitate collected to yield the title compound.
Workup
- customthe solvent evaporated
- dissolutionThe residue is dissolved in methanol
- additionadded to diethyl ether
- customthe precipitate collected
Sources & evidence
- ORD record
- ord-70b1e0cc27e8411d82ffa2ede26c0f25
- Source dataset
- uspto-grants-1978_03
- Patent number
- US04081530
Reaction notes
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