Diisopropylethylamine → HCID 59170070, compound

HRID 1446316Notes

Reaction equation

HRID 1446316 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([C:56]2([OH:62])[CH2:61][CH2:60][NH:59][CH2:58][CH2:57]2)[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=1>CN(C=O)C.C(Cl)(Cl)Cl>[OH:62][C:56]1([C:50]2[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=2)[CH2:61][CH2:60][N:59]([C:29]([C:28]2[C:24]([CH3:23])=[N:25][O:26][C:27]=2[CH2:32][C:33]([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)=[O:40])=[O:31])[CH2:58][CH2:57]1

Participants

7

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 4-phenylpiperidin-4-ol (0.18 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 C24H24N2O4: 404.1736, found 404.1732.

Workup

  1. washthe solution was washed with water and 1 M HCl
  2. dry with materialdried (Na2SO4)
  3. customevaporated
  4. customThe residue was purified by flash chromatography (SiO2 1:2 heptane/EtOAc)

Sources & evidence

ORD record
ord-fbe19a6c5aed4feb8867c4f5e06cf492
Source dataset
uspto-grants-2010_02
Patent number
US07666888B2

Reaction notes

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