Hydrochloric Acid → HCID 67205028, compound
Reaction equation
C([O:3][C:4]([CH:6]1[CH2:11][CH2:10][N:9]([CH2:12][C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:8][CH:7]1[C:19]1[CH:23]=[CH:22][S:21][CH:20]=1)=[O:5])C.Cl>>[CH2:12]([N:9]1[CH2:10][CH2:11][CH:6]([C:4]([OH:5])=[O:3])[CH:7]([C:19]2[CH:23]=[CH:22][S:21][CH:20]=2)[CH2:8]1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1Participants
3
Procedure
The product from step c) (4.78 g, 14.5 mmol) was treated with 4 M HCl at 100° C. for 16 hours. Next, the reaction was evaporated to dryness, azeotroped with toluene (2×50 ml) and placed on the high vacuum to give the subtitle compound. MS calculated for C17H19NO2S−H 300, observed 300.
Workup
- customNext, the reaction was evaporated to dryness
- customazeotroped with toluene (2×50 ml)
Sources & evidence
- ORD record
- ord-4dc042578c4b4a0192d3e358b14f5c06
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07423056B2
Reaction notes
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