Ethyl Acetate → HCID 59737296, compound
Reaction equation
[Si]([O:18][CH2:19][C:20]1[S:24][C:23]([C:25]2[CH:30]=[CH:29][C:28]([NH:31][C:32](=[O:38])[O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[C:27]([NH:39][C:40](=[O:53])[C:41]3[CH:46]=[CH:45][C:44]([C:47]4[CH:48]=[N:49][CH:50]=[CH:51][CH:52]=4)=[CH:43][CH:42]=3)[CH:26]=2)=[CH:22][CH:21]=1)(C(C)(C)C)(C1C=CC=CC=1)C1C=CC=CC=1.CCOC(C)=O>C(Cl)Cl>[OH:18][CH2:19][C:20]1[S:24][C:23]([C:25]2[CH:30]=[CH:29][C:28]([NH:31][C:32](=[O:38])[O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[C:27]([NH:39][C:40](=[O:53])[C:41]3[CH:42]=[CH:43][C:44]([C:47]4[CH:48]=[N:49][CH:50]=[CH:51][CH:52]=4)=[CH:45][CH:46]=3)[CH:26]=2)=[CH:22][CH:21]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Following the same procedure as described in Example 20, step 5 (scheme 20) but substituting compound 189 for compound 198, title compound 199 was obtained in 90% yield [after column chromatography (eluent: 25% AcOEt in DCM)].
Sources & evidence
- ORD record
- ord-0f70abb40f92493fa893d7473f3311c3
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08598168B2
Reaction notes
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