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HCID 54200145, compound → HCID 54282494, compound

HRID 1733341
Notes
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Reaction equation

HRID 1733341 reaction equation
C([S:4][CH:5]([C:16]([F:19])([F:18])[F:17])[C:6]([N:8]1[CH2:15][CH2:14][CH2:13][C@H:9]1[C:10]([OH:12])=[O:11])=[O:7])(=O)C>O.N>[SH:4][CH:5]([C:16]([F:19])([F:17])[F:18])[C:6]([N:8]1[CH2:15][CH2:14][CH2:13][C@H:9]1[C:10]([OH:12])=[O:11])=[O:7]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 1

HCID 54200145HCID 54200145, compound

Product 1

HCID 54282494HCID 54282494, compound

Reagents, catalysts & solvents 2

HCID 222AmmoniaSolventHCID 962WaterSolvent

Procedure

1-(2-Acetylthio-3,3,3-trifluoropropanoyl)-L-proline (4 g.) is dissolved in a mixture of water (8 ml.) and concentrated ammonia (8 ml.) under a blanket of nitrogen. After thirty minutes at room temperature, the reaction mixture is acidified and extracted with ethyl acetate. The organic phase is dried over magnesium sulfate and concentrated to dryness in vacuo to yield 1-(2-mercapto-3,3,3-trifluoropropanoyl)-L-proline.

Workup

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes
  • waitAfter thirty minutes at room temperature
  • extractionextracted with ethyl acetate
  • dry with materialThe organic phase is dried over magnesium sulfate
  • concentrationconcentrated to dryness in vacuo
  • Sources & evidence

    ORD record
    ord-3bd01a04bc974cb69a4f6b647aa0c1c6
    Source dataset
    uspto-grants-1980_12
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04241076

    Reaction notes

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