Reaction equation
I[C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8]CC)=[O:7])=[CH:4][CH:3]=1.[CH3:13][C@@H:14]1[CH2:18][O:17][C:16](=[O:19])[NH:15]1>>[CH3:13][C@@H:14]1[CH2:18][O:17][C:16](=[O:19])[N:15]1[C:2]1[CH:3]=[CH:4][C:5]([C:6]([OH:8])=[O:7])=[CH:11][CH:12]=1Participants
3
Procedure
By reaction and treatment in the same manner as in Preparation Example 18 and using ethyl 4-iodobenzoate (1.4 mL) and (R)-4-methyloxazolidin-2-one (860 mg) described in Preparation Example 25, the title compound (0.9 g) was obtained.
Workup
- customBy reaction and treatment in the same manner
- customas in Preparation Example 18
- customdescribed in Preparation Example 25
Sources & evidence
- ORD record
- ord-e84e8c1253ee489a82819b91954e3aab
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08354401B2
Linked notes
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