Diisopropylethylamine → 3-(1-{[3-(3-Chloro-4-methoxyphenyl)isoxazol-4-yl]carbonyl}pyrrolidin-3-yl)pyridine
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:10]2[C:14]([C:15]([OH:17])=O)=[CH:13][O:12][N:11]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].C(N(C(C)C)C(C)C)C.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[NH:49]1[CH2:53][CH2:52][CH:51]([C:54]2[CH:55]=[N:56][CH:57]=[CH:58][CH:59]=2)[CH2:50]1>CN(C=O)C>[Cl:1][C:2]1[CH:3]=[C:4]([C:10]2[C:14]([C:15]([N:49]3[CH2:53][CH2:52][CH:51]([C:54]4[CH:55]=[N:56][CH:57]=[CH:58][CH:59]=4)[CH2:50]3)=[O:17])=[CH:13][O:12][N:11]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 3-(3-chloro-4-methoxyphenyl)isoxazole-4-carboxylic acid (10 mg, 0.04 mmol), N-ethyl-N-isopropylpropan-2-amine (14 μL, 0.08 mmol, 2 equ.) and TBTU (15 mg, 0.046 mmol, 1.2 equ.) in DMF (0.3 mL) was added to 3-pyrrolidin-3-ylpyridine (6 mg, 0.04 mmol). After 1 h at rt the crude product was purified by RP-HPLC. The pure fractions were basified (NaHCO3) and extracted with ethyl acetate, dried (Na2SO4), evaporated and dried in vacuum to yield the title compound (10 mg). MS (ESI, pos. ion) m/z 384 (M+1); HRMS, calcd for C20H18ClN3O3: 383.1037, found 383.1033.
Workup
- customAfter 1 h at rt the crude product was purified by RP-HPLC
- extractionextracted with ethyl acetate
- dry with materialdried (Na2SO4)
- customevaporated
- customdried in vacuum
Sources & evidence
- ORD record
- ord-8cdb123c9bca439eb050a3dc8c111105
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07666888B2
Reaction notes
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