Hydrochloric Acid → HCID 68836874, compound
Reaction equation
[CH3:1][N:2]([CH3:24])[C:3](=[O:23])[CH:4](NC(=O)OC(C)(C)C)[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:14])([F:13])[F:12])[CH:6]=1.[ClH:25]>O1CCOCC1>[ClH:25].[CH3:24][N:2]([CH3:1])[C:3](=[O:23])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([F:13])([F:12])[F:14])[CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
130 mg (375 μmol) of the compound from Example 174A are stirred at RT in 2 ml of a 4 M solution of hydrogen chloride in dioxan. After complete conversion, the volatile components are removed on the rotary evaporator and the residue dried under high vacuum. 105 mg (99% of theory) of the title compound are obtained.
Workup
- customAfter complete conversion, the volatile components are removed on the rotary evaporator
- customthe residue dried under high vacuum
Sources & evidence
- ORD record
- ord-6a5ab579e85447cda0669804a4067e15
- Source dataset
- uspto-grants-2011_12
- Patent number
- US08084481B2
Reaction notes
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