Diisopropylethylamine → HCID 59170179, compound
Reaction equation
CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[CH3:23][C:24]1[C:28]([C:29]([OH:31])=O)=[C:27]([CH2:32][C:33](=[O:40])[C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)[O:26][N:25]=1.C(N(C(C)C)C(C)C)C.[C:50]1([CH:56]2[CH2:60][CH2:59][NH:58][CH2:57]2)[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=1>CN(C=O)C.C(Cl)(Cl)Cl>[CH3:23][C:24]1[C:28]([C:29]([N:58]2[CH2:59][CH2:60][CH:56]([C:50]3[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=3)[CH2:57]2)=[O:31])=[C:27]([CH2:32][C:33]([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)=[O:40])[O:26][N:25]=1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of TBTU (0.48 g, 1.5 mmol, 1.5 eq.) in DMF (2 mL) was added to a mixture of 3-methyl-5-(2-oxo-2-phenylethyl)isoxazole-4-carboxylic acid (0.24 g, 1 mmol, 1 eq), N-ethyl-N-isopropylpropan-2-amine (0.18 mL, 1 eq) and 3-phenylpyrrolidine (0.15 g, 1 eq) in DMF (1 mL). The resulting solution was stirred at room temperature. Chloroform (25 mL) was added and the solution was washed with water and 1 M HCl, dried (Na2SO4) and evaporated. The residue was purified by flash chromatography (SiO2 1:2 heptane/EtOAc) to afford the title compound. MS (ESI, POS. ION) M/Z Calcd for C23H22N2O3: 374.1630, found 374.1632.
Workup
- washthe solution was washed with water and 1 M HCl
- dry with materialdried (Na2SO4)
- customevaporated
- customThe residue was purified by flash chromatography (SiO2 1:2 heptane/EtOAc)
Sources & evidence
- ORD record
- ord-0e914284f9c84822bf2f9d33b1ef94c4
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666888B2
Reaction notes
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