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

HRID 1039208Notes

Reaction equation

HRID 1039208 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[O:21][CH3:22])#[CH:14].[CH2:23]([O:25][C:26](=[O:35])[CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][N+:32]([O-])=[O:33])[CH3:24].C(N(CC)CC)C>C1(C)C=CC=CC=1>[CH2:23]([O:25][C:26](=[O:35])[CH2:27][CH2:28][CH2:29][CH2:30][C:31]1[CH:14]=[C:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=2[O:21][CH3:22])[O:33][N:32]=1)[CH3:24]

Participants

6

Procedure

Add 1,4-phenylenediisocyanate (14.5 g, 90.8 mmol) to a stirred solution of 1-ethynyl-2-methoxy-benzene (4.0 g, 30.3 mmol) and 6-nitro-hexanoic acid ethyl ester (8.6 g, 45.4 mmol) in toluene (300 mL, anhydrous) and stir under N2. Add triethylamine (12.7 mL, 90.8 mmol) and heat to reflux under N2. After 2.5 hours, filter mixture through a pad of Celite® and rinse with toluene. Concentrate to get 9 grams of a orange oil. Adsorb on SiO2 and purify the residue by flash chromatography on silica gel eluting with 0-20% EtOAc/hexanes to afford the title compound (14.0 g, 74%).

Workup

  1. temperatureto reflux under N2
  2. filtrationfilter mixture through a pad of Celite®
  3. washrinse with toluene
  4. concentrationConcentrate

Sources & evidence

ORD record
ord-9c04656f75d44109960c7483bb5ce314
Source dataset
uspto-grants-2013_10
Patent number
US08552039B2

Reaction notes

Loading…