HCID 67206140, compound → HCID 67206083, 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[S:20][CH:21]=[CH:22][CH:23]=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[S:20][CH:21]=[CH:22][CH:23]=2)[CH2:8]1)[C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
The product from step b) (2.9 g, 8.8 mmol) was treated with 4 M HCl (200 ml) 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 (2.9 g, 98%). 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-bbfb62f3083a45d2b831ac2e73855e87
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07423056B2
Reaction notes
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