HCID 57299275, compound → HCID 18689715, compound
Reaction equation
[CH2:1]([C:3]1[CH:44]=[CH:43][C:6]2[CH:7]([C:17]3[C:18](=[O:42])[NH:19][C:20](=[O:41])[N:21]([C:23]4[N:28]=[C:27]([NH:29][CH2:30][C:31]([O:33]C(C)(C)C)=[O:32])[C:26]([N+:38]([O-:40])=[O:39])=[CH:25][N:24]=4)[CH:22]=3)[C:8]3[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][C:9]=3[CH:10]=[CH:11][C:5]=2[CH:4]=1)[CH3:2]>ClCCl.FC(F)(F)C(O)=O>[CH2:1]([C:3]1[CH:44]=[CH:43][C:6]2[CH:7]([C:17]3[C:18](=[O:42])[NH:19][C:20](=[O:41])[N:21]([C:23]4[N:28]=[C:27]([NH:29][CH2:30][C:31]([OH:33])=[O:32])[C:26]([N+:38]([O-:40])=[O:39])=[CH:25][N:24]=4)[CH:22]=3)[C:8]3[CH:15]=[CH:14][C:13]([CH3:16])=[CH:12][C:9]=3[CH:10]=[CH:11][C:5]=2[CH:4]=1)[CH3:2]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of the product from example 28 step (ii) (0.07 g) in dichloromethane (1 ml) and trifluoroacetic acid (1 ml) was stirred overnight and evaporated. The residue was triturated with ether and filtered off. Yield 0.05 g.
Workup
- customevaporated
- customThe residue was triturated with ether
- filtrationfiltered off
Sources & evidence
- ORD record
- ord-8a01ac1f87fd4999806f26c5380aeb5c
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06107297
Reaction notes
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