Diisopropylethylamine → 2-((3R)-1-{[3-(4-methoxyphenyl)isoxazol-4-yl]carbonyl}piperidin-3-yl)propan-2-ol

HRID 1446351Notes

Reaction equation

HRID 1446351 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.Cl.[NH:49]1[CH2:54][CH2:53][CH2:52][C@@H:51]([C:55]([OH:58])([CH3:57])[CH3:56])[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:49]3[CH2:54][CH2:53][CH2:52][C@@H:51]([C:55]([OH:58])([CH3:57])[CH3:56])[CH2:50]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 2-[(3R)-piperidin-3-yl]propan-2-ol hydrochloride (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 (8 mg). MS (ESI, pos. ion) m/z: calcd for C19H24N2O4: 344.1736, found 344.1737.

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-a0d01ee58e2b46d6b0a037446b311d47
Source dataset
uspto-grants-2010_02
Patent number
US07666888B2

Reaction notes

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