HCID 42623375, compound → HCID 67241859, compound

HRID 2424639Notes

Reaction equation

HRID 2424639 reaction equation
C[C@@H]1NCCN(CC2C=CC(NS(C3C=NC(N4CCCCC4)=CC=3)(=O)=O)=CC=2)C1.[CH3:31][C@H:32]1[CH2:37][N:36]([CH2:38][C:39]2[CH:44]=[CH:43][C:42]([NH:45][S:46]([C:49]3[CH:50]=[N:51][C:52]([N:55]4[CH2:60][CH2:59][O:58][CH2:57][CH2:56]4)=[CH:53][CH:54]=3)(=[O:48])=[O:47])=[CH:41][CH:40]=2)[CH2:35][CH2:34][N:33]1C(OC(C)(C)C)=O>>[CH3:31][C@@H:32]1[NH:33][CH2:34][CH2:35][N:36]([CH2:38][C:39]2[CH:44]=[CH:43][C:42]([NH:45][S:46]([C:49]3[CH:50]=[N:51][C:52]([N:55]4[CH2:56][CH2:57][O:58][CH2:59][CH2:60]4)=[CH:53][CH:54]=3)(=[O:48])=[O:47])=[CH:41][CH:40]=2)[CH2:37]1

Participants

3

Reactant 2

HCID 42623375HCID 42623375, compoundHCID 59532415HCID 59532415, compound

Product 1

HCID 67241859HCID 67241859, compound

Procedure

The title compound was prepared in a similar manner to E3 using 1,1-dimethylethyl (2S)-2-methyl-4-{[4-({[6-(4-morpholinyl)-3-pyridinyl]sulfonyl}amino)phenyl]methyl}-1-piperazinecarboxylate (D18). MS (ES+): MH+ 432.3

Sources & evidence

ORD record
ord-4409ac291b8f4c47ac090b0934f05d05
Source dataset
uspto-grants-2011_06
Patent number
US07964597B2

Reaction notes

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