Chloroform → HCID 131717905, compound
Reaction equation
[CH:1]1([N:4]2[C:13]3[C:8](=[CH:9][C:10]([F:26])=[C:11]([N:14]4[CH2:19][CH2:18][NH:17][CH:16]([C:20]5[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=5)[CH2:15]4)[CH:12]=3)[C:7](=[O:27])[C:6]([C:28]([OH:30])=[O:29])=[CH:5]2)[CH2:3][CH2:2]1.C(Cl)(Cl)[Cl:32].CN(C)C=O>C(O)C.Cl>[ClH:32].[CH:1]1([N:4]2[C:13]3[C:8](=[CH:9][C:10]([F:26])=[C:11]([N:14]4[CH2:19][CH2:18][NH:17][CH:16]([C:20]5[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=5)[CH2:15]4)[CH:12]=3)[C:7](=[O:27])[C:6]([C:28]([OH:30])=[O:29])=[CH:5]2)[CH2:2][CH2:3]1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A 54 mg portion of the base compound from Example 128 was dissolved, with heat, in a mixture of ethanol, chloroform and a little dimethylformamide. A few drops of concentrated hydrochloric acid were added, the solid was collected, washed with water, ether and dried, giving 35 mg of the desired product.
Workup
- customthe solid was collected
- washwashed with water, ether
- customdried
Sources & evidence
- ORD record
- ord-e7ea54ae83e0496f99beb7c0cc5ad309
- Source dataset
- uspto-grants-1993_05
- Patent number
- US05210193
Reaction notes
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