Triethylamine → HCID 68867633, compound
Reaction equation
[NH2:1][C:2]1[CH:34]=[CH:33][C:32]([Cl:35])=[CH:31][C:3]=1[C:4]([NH:6][C@@H:7]([CH2:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=2[O:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[CH:14][CH:13]=1)[C:8]([OH:10])=[O:9])=[O:5].[CH3:36]OC(=O)[C@@H](N)CC1C=CC(C2C=CC=CC=2OC2C=CC=CC=2)=CC=1.NC1C=CC(Cl)=CC=1C(O)=O.[CH3:73][S:74][C:75]1[CH:80]=[CH:79][C:78](B(O)O)=[CH:77][CH:76]=1.C(N(CC)CC)C>C([O-])(=O)C.[Cu+2].C([O-])(=O)C>[CH3:36][O:9][C:8](=[O:10])[CH:7]([NH:6][C:4](=[O:5])[C:3]1[CH:31]=[C:32]([Cl:35])[CH:33]=[CH:34][C:2]=1[NH:1][C:78]1[CH:79]=[CH:80][C:75]([S:74][CH3:73])=[CH:76][CH:77]=1)[CH2:11][C:12]1[CH:13]=[CH:14][C:15]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=2[O:24][C:25]2[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=2)=[CH:16][CH:17]=1Participants
Procedure
A solution of (2S)-(2-amino-5-chloro-benzoylamino)-3-(2′-phenoxy-biphenyl-4-yl)-propionic acid (0.154 g, 0.307 mmol), prepared by reacting (2S)-amino-3-(2′-phenoxy-biphenyl-4-yl)-propionic acid methyl ester and 2-amino-5-chlorobenzoic acid by the general procedure A) was reacted with 4-(methylthio)phenylboronic acid (0.130 g, 0.768 mmol), copper acetate (0.084 g, 0.460 mmol), and triethyl amine (0.215 mL, 1.535 mmol) by the general procedure G. The crude product was purified by flash column chromatography on silica gel using DCM containing 25% hexane to give 0.075 g of 2-[5-chloro-2-(4-methylsulfanyl-phenylamino)-benzoylamino]-3-(2′-phenoxy-biphenyl-4-yl)-propionic acid methyl ester as an oil. This ester was treated with LiOH (0.019 g, 0.441 mmol) by the general procedure I to give 0.049 g of 2-[5-chloro-2-(4-methylsulfanyl-phenylamino)-benzoylamino]-3-(2′-phenoxy-biphenyl-4-yl)-propionic acid.
Workup
- customThe crude product was purified by flash column chromatography on silica gel
Sources & evidence
- ORD record
- ord-6f89defbd0054c18abde4c6817aac2b9
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07544699B2
Reaction notes
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