HCID 131722512, compound → HCID 131722511, compound
Reaction equation
[CH2:1]([C:3]1[CH:4]=[CH:5][C:6]2[C:16]([C:18]3[C:19](=[O:36])[NH:20][C:21](=[O:35])[N:22]([CH2:24][C:25]4[CH:26]=[C:27]([CH:32]=[CH:33][CH:34]=4)[C:28]([O:30][CH3:31])=[O:29])[CH:23]=3)(O)[C:11]3[N:12]=[C:13]([CH3:15])[S:14][C:10]=3[CH2:9][CH2:8][C:7]=2[CH:37]=1)[CH3:2]>C(O)(=O)C>[CH2:1]([C:3]1[CH:4]=[CH:5][C:6]2[CH:16]([C:18]3[C:19](=[O:36])[NH:20][C:21](=[O:35])[N:22]([CH2:24][C:25]4[CH:26]=[C:27]([CH:32]=[CH:33][CH:34]=4)[C:28]([O:30][CH3:31])=[O:29])[CH:23]=3)[C:11]3[N:12]=[C:13]([CH3:15])[S:14][C:10]=3[CH:9]=[CH:8][C:7]=2[CH:37]=1)[CH3:2]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of the product from step (iv) (0.18 g) in glacial acetic acid (6 ml) was stirred at 100° C. for 2 hours. The solution was evaporated to dryness (azeotroped twice with toluene) and the residue purified by chromatography eluting with ethyl acetate.
Workup
- customThe solution was evaporated to dryness (
- customazeotroped twice with toluene) and the residue
- custompurified by chromatography
- washeluting with ethyl acetate
Sources & evidence
- ORD record
- ord-521c66cda8b844228ed37ed4baeec2e0
- Source dataset
- uspto-grants-2001_04
- Patent number
- US06218376B1
Reaction notes
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