Pyrimidine-5-carboxylic acid → 3-Chloro-3'-fluoro-4'-[(R)-1-({3-[(pyrimidine-5-carbonyl)-amino]-oxetane-3-carbonyl}-amino)-ethyl]-biphenyl-2-carboxylic acid methyl ester
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[C:6]([C:12]2[CH:17]=[CH:16][C:15]([C@H:18]([NH:20][C:21]([C:23]3([NH2:27])[CH2:26][O:25][CH2:24]3)=[O:22])[CH3:19])=[C:14]([F:28])[CH:13]=2)=[CH:7][CH:8]=[CH:9][C:10]=1[Cl:11])=[O:4].[N:29]1[CH:34]=[C:33]([C:35](O)=[O:36])[CH:32]=[N:31][CH:30]=1>>[CH3:1][O:2][C:3]([C:5]1[C:6]([C:12]2[CH:17]=[CH:16][C:15]([C@H:18]([NH:20][C:21]([C:23]3([NH:27][C:35]([C:33]4[CH:34]=[N:29][CH:30]=[N:31][CH:32]=4)=[O:36])[CH2:24][O:25][CH2:26]3)=[O:22])[CH3:19])=[C:14]([F:28])[CH:13]=2)=[CH:7][CH:8]=[CH:9][C:10]=1[Cl:11])=[O:4]Participants
3
Reactant 2
Product 1
Procedure
The title compound was prepared in analogy to example 1 using intermediate 4 instead of intermediate 1 and pyrimidine-5-carboxylic acid instead of 3-fluoro-5-(trifluoromethyl)benzoic acid and was obtained as white solid. MS: 513.2 [M+H]+.
Workup
- customwas obtained as white solid
Sources & evidence
- ORD record
- ord-ea5f3cdc1d584315bb05dabbe818923f
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08912221B2
Reaction notes
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