HCID 11075603, compound → HCID 11490373, compound

HRID 899485Notes

Reaction equation

HRID 899485 reaction equation
[CH3:1][N:2]([C:7]1[CH:8]=[C:9]([CH:22]=[C:23]([CH2:25]Br)[CH:24]=1)[C:10]([NH:12][C@@H:13]([C:15]1[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=1)[CH3:14])=[O:11])[S:3]([CH3:6])(=[O:5])=[O:4].[NH2:27][C:28]([CH2:38][C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1)([CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[CH2:29][OH:30].NC(CC1C=CC=CC=1)(CCCC)COCC1C=C(C=C(N(C)S(C)(=O)=O)C=1)C(N[C@@H](C1C=CC(F)=CC=1)C)=O>>[NH2:27][C:28]([CH2:38][C:39]1[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=1)([CH2:31][C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1)[CH2:29][O:30][CH2:25][C:23]1[CH:22]=[C:9]([CH:8]=[C:7]([N:2]([CH3:1])[S:3]([CH3:6])(=[O:5])=[O:4])[CH:24]=1)[C:10]([NH:12][C@@H:13]([C:15]1[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=1)[CH3:14])=[O:11]

Participants

4

Reactant 3

HCID 11075603HCID 11075603, compoundHCID 16094314HCID 16094314, compoundHCID 58856333HCID 58856333, compound

Product 1

HCID 11490373HCID 11490373, compound

Procedure

Prepared from 3-(N-methyl-N-(methylsulfonyl)amino)-5-(bromomethyl)-N-((R)-1-(4-fluorophenyl)ethyl)benzamide and 2-amino-2-benzyl-3-phenylpropan-1-ol using a similar procedure as described for the preparation of 3-{[(2-amino-2-benzylhexyl)oxy]methyl}-N-[(1R)-1-(4-fluorophenyl)ethyl]-5-[methyl(methyl sulfonyl)amino]benzamide (Example 4). HRMS ES calculated for C34H38FN3O4S: 604.2640, found: 604.2641.

Sources & evidence

ORD record
ord-34033d25338f4e6baa1dce68dc39c03e
Source dataset
uspto-grants-2008_04
Patent number
US07354942B2

Reaction notes

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