Bromoacetic Acid → HCID 59430591, compound
Reaction equation
Br[CH2:2][C:3]([OH:5])=O.CCN=C=NCCCN(C)C.[ClH:17].[NH2:18][C:19]1[CH:20]=[C:21]([C:26]2[N:27]([CH2:39][CH3:40])[C:28]3[C:33]([C:34]=2[C:35]#[N:36])=[CH:32][CH:31]=[C:30]([O:37][CH3:38])[CH:29]=3)[CH:22]=[CH:23][C:24]=1[OH:25]>C(#N)C>[Cl:17][CH2:2][C:3]([NH:18][C:19]1[CH:20]=[C:21]([C:26]2[N:27]([CH2:39][CH3:40])[C:28]3[C:33]([C:34]=2[C:35]#[N:36])=[CH:32][CH:31]=[C:30]([O:37][CH3:38])[CH:29]=3)[CH:22]=[CH:23][C:24]=1[OH:25])=[O:5]Participants
5
Procedure
Bromoacetic acid (52 mg, 0.37 mmol) is combined with EDCI hydrochloride (62 mg, 0.4 mmol) and acetonitrile (900 μL) to form a homogeneous solution. 2-(3-Amino-4-hydroxyphenyl)-1-ethyl-6-methoxy-1H-indole-3-carbonitrile (100 mg, 0.33 mmol), prepared as in example 1BG, step B, is added to the solution. A thick paste soon forms. Another 1.1 mL of acetonitrile is added and the mixture is then stirred at room temperature for 2 hours. The reaction mixture is then partitioned between H2O and EtOAc. The organic layer is dried and concentrated. Purification by silica gel chromatography (4/1, CH2Cl2/EtOAc) yields 2-chloro-N-[5-(3-cyano-1-ethyl-6-methoxy-1H-indol-2-yl)-2-hydroxyphenyl]acetamide (82 mg, 60%), compound 333, as a white solid.
Workup
- customto form a homogeneous solution
- additionis added to the solution
- customThe reaction mixture is then partitioned between H2O and EtOAc
- customThe organic layer is dried
- concentrationconcentrated
- customPurification by silica gel chromatography (4/1, CH2Cl2/EtOAc)
Sources & evidence
- ORD record
- ord-76f98de02b7846df9da91115c3cd7c88
- Source dataset
- uspto-grants-2011_01
- Patent number
- US07868037B2
Reaction notes
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