Triethylamine → 5-[5-(2-Acetylamino-phenyl)-isoxazol-3-yl]-pentanoic acid ethyl ester

HRID 1443729Notes

Reaction equation

HRID 1443729 reaction equation
C1(N=C=O)C=CC(N=C=O)=CC=1.[C:13]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[NH:21][C:22](=[O:24])[CH3:23])#[CH:14].[CH2:25]([O:27][C:28](=[O:37])[CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][N+:34]([O-])=[O:35])[CH3:26].C(N(CC)CC)C>C1(C)C=CC=CC=1>[CH2:25]([O:27][C:28](=[O:37])[CH2:29][CH2:30][CH2:31][CH2:32][C:33]1[CH:14]=[C:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[NH:21][C:22](=[O:24])[CH3:23])[O:35][N:34]=1)[CH3:26]

Participants

6

Reactant 4

HCID 8471TriethylamineHCID 610091,4-DiisocyanatobenzeneHCID 10261360N-(2-ethynylphenyl)acetamideHCID 13717120Ethyl 6-nitrohexanoate

Product 1

HCID 591677705-[5-(2-Acetylamino-phenyl)-isoxazol-3-yl]-pentanoic acid ethyl esterYield 116.6%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

Add 1,4-phenylenediisocyanate (5.15 g, 32.2 mmol) to a stirred solution of N-(2-ethynyl-phenyl)-acetamide (2.56 g, 16.1 mmol) and 6-nitro-hexanoic acid ethyl ester (4.56 g, 24.1 mmol) in toluene (200 mL, anhydrous) and stir under N2. Add triethylamine (4.5 mL, 32.2 mmol) and heat to reflux under N2 overnight. Filter. mixture through a pad of Celite® and rinse with toluene. Concentrate to get 6.2 g yellow oil. Adsorb on SiO2 and purify the residue by flash chromatography on silica gel eluting with 0-60% EtOAc/hexanes to afford the title compound (4.02 g, 76%). Correct regioisomer is confirmed by NOESY. MS (IS) 331 (M+1)+.

Workup

  1. temperatureto reflux under N2 overnight
  2. filtrationFilter
  3. washmixture through a pad of Celite® and rinse with toluene
  4. concentrationConcentrate

Sources & evidence

ORD record
ord-d63a7496ffe945168de3feb8af47c681
Source dataset
uspto-grants-2010_02
Patent number
US07662771B2

Reaction notes

Loading…