Diisopropylethylamine → HCID 86650423, compound
Reaction equation
CCN(C(C)C)C(C)C.[OH:10][C:11]1[CH:12]=[CH:13][CH:14]=[C:15]2[C:20]=1[O:19][C:18](=[O:21])[C:17]([C:22]([OH:24])=O)=[CH:16]2.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[CH3:49][O:50][C:51]1[N:56]=[C:55]([O:57][CH3:58])[C:54]([C:59]2[CH:60]=[C:61]([NH2:65])[CH:62]=[CH:63][CH:64]=2)=[CH:53][N:52]=1>CN(C=O)C>[CH3:49][O:50][C:51]1[N:56]=[C:55]([O:57][CH3:58])[C:54]([C:59]2[CH:60]=[C:61]([NH:65][C:22]([C:17]3[C:18](=[O:21])[O:19][C:20]4[C:15]([CH:16]=3)=[CH:14][CH:13]=[CH:12][C:11]=4[OH:10])=[O:24])[CH:62]=[CH:63][CH:64]=2)=[CH:53][N:52]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
DIEA (0.012 mL, 0.071 mmol) was added to 8-hydroxy-3-carboxy-coumarin (0.013 g, 0.065 mmol) and HATU (0.027 g, 0.071 mmol) in 0.5 mL of DMF with constant stirring at room temperature until a clear solution resulted. Subsequently, 3-(2,4-dimethoxy-pyrimidin-5-yl)-phenylamine (0.015 g, 0.065 mmol) was added and allowed to react overnight. DMF was removed under vacuum and the reaction was resuspended in DMSO. The crude product was purified on a Parallex Flex parallel preparative reverse phase HPLC instrument (Biotage) using a solvent gradient of 10-95% ACN/H2O with 0.05% TFA at a flow rate of 20 mL/min. UV absorbance was monitored at 254 nm and the fractions corresponding to the product peak were collected and the solvent removed under vacuum to give 0.010 g of product in 39% yield: LCMS (ESI) m/z 420 (MH+).
Workup
- customresulted
- customto react overnight
- customDMF was removed under vacuum
- customThe crude product was purified on a Parallex Flex parallel preparative reverse phase HPLC instrument (Biotage)
- customthe fractions corresponding to the product peak were collected
- customthe solvent removed under vacuum
Sources & evidence
- ORD record
- ord-58591cb8e14f47baa78b146415be43d7
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08642788B2
Reaction notes
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