Diisopropylethylamine → 1-{[3-(4-Methoxyphenyl)isoxazol-4-yl]carbonyl}-5-methyl-3-phenylpyrrolidin-3-ol

HRID 1446349Notes

Reaction equation

HRID 1446349 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:13]([C:14]([OH:16])=O)=[CH:12][O:11][N:10]=2)=[CH:5][CH:4]=1.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.[CH3:48][CH:49]1[NH:53][CH2:52][C:51]([C:55]2[CH:60]=[CH:59][CH:58]=[CH:57][CH:56]=2)([OH:54])[CH2:50]1>CN(C=O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]2[C:13]([C:14]([N:53]3[CH:49]([CH3:48])[CH2:50][C:51]([C:55]4[CH:60]=[CH:59][CH:58]=[CH:57][CH:56]=4)([OH:54])[CH2:52]3)=[O:16])=[CH:12][O:11][N:10]=2)=[CH:7][CH:8]=1

Participants

6

Procedure

A solution of 3-(4-methoxyphenyl)isoxazole-4-carboxylic acid (7 mg, 0.03 mmol), N-ethyl-N-isopropylpropan-2-amine (16 μL, 0.09 mmol, 3 equ.) and TBTU (12 mg, 0.036 mmol, 1.2 equ.) in DMF (0.3 mL) was added to 5-methyl-3-phenylpyrrolidin-3-ol (5 mg, 0.03 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 (6 mg). MS (ESI, pos. ion) m/z: calcd for C22H22N2O4: 378.1580, found 378.1580.

Workup

  1. customAfter 1 h at rt the crude product was purified by RP-HPLC
  2. extractionextracted with ethyl acetate
  3. dry with materialdried (Na2SO4)
  4. customevaporated
  5. customdried in vacuum

Sources & evidence

ORD record
ord-4adbe9649d6d4cdd910d77ee46dc74d4
Source dataset
uspto-grants-2010_02
Patent number
US07666888B2

Reaction notes

Loading…