Ammonia → 1-(3-Mercapto-1-oxopropyl)-L-proline
Reaction equation
C([O:5][C:6](=[O:20])[C@@H:7]1[CH2:11][CH2:10][CH2:9][N:8]1[C:12](=[O:19])[CH2:13][CH2:14][S:15]C(=O)C)(C)(C)C.N>>[SH:15][CH2:14][CH2:13][C:12]([N:8]1[CH2:9][CH2:10][CH2:11][C@H:7]1[C:6]([OH:20])=[O:5])=[O:19]Participants
Procedure
The product from Example 2, 3-acetylthiopropanoyl-L-proline-t-butyl ester, 0.5 g, was mixed with 4.5 ml of 5.5N methanolic ammonia at room temperature under nitrogen for one hour to remove the acetyl group. The solvent was then removed at 25° C. with a rotary evaporator. After the product was taken up in methanol and reevaporated twice more in the rotary evaporator, the clear oily residue was dissolved in ethyl ether, washed twice with 5% potassium bisulphate and once with saturated NaCl, dried over MgSO4 and filtered. Residual solvent was removed in vacuo to yield a clear oily product, migrating as a single spot on thin layer chromatography in three separate solvent systems. The t-butyl ester protecting group was removed by reaction with trifluoroacetic acid in anisole.
Workup
- customto remove the acetyl group
- customThe solvent was then removed at 25° C. with a rotary evaporator
- customreevaporated twice more in the rotary evaporator
- dissolutionthe clear oily residue was dissolved in ethyl ether
- washwashed twice with 5% potassium bisulphate and once with saturated NaCl
- dry with materialdried over MgSO4
- filtrationfiltered
- customResidual solvent was removed in vacuo
- customto yield a clear oily product
- customseparate solvent systems
- customThe t-butyl ester protecting group was removed by reaction with trifluoroacetic acid in anisole
Sources & evidence
- ORD record
- ord-8d3034b384f3476b86f525cab67b7ebc
- Source dataset
- uspto-grants-1987_10
- Patent number
- US04698356
Reaction notes
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