HCID 59275665, compound → HCID 59275241, compound

HRID 1025068Notes

Reaction equation

HRID 1025068 reaction equation
[C:1]([O:5][C:6]([C:8]1[CH:9]=[C:10]([C:14]2[C:15]([N+:35]([O-])=O)=[CH:16][C:17]3[O:21][C:20]([C:22]4[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=4)=[C:19]([C:29]([O:31][CH2:32][CH3:33])=[O:30])[C:18]=3[CH:34]=2)[CH:11]=[CH:12][CH:13]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>CCO.CC(O)=O.CCOC(C)=O.[Fe]>[NH2:35][C:15]1[C:14]([C:10]2[CH:11]=[CH:12][CH:13]=[C:8]([C:6]([O:5][C:1]([CH3:2])([CH3:4])[CH3:3])=[O:7])[CH:9]=2)=[CH:34][C:18]2[C:19]([C:29]([O:31][CH2:32][CH3:33])=[O:30])=[C:20]([C:22]3[CH:23]=[CH:24][C:25]([F:28])=[CH:26][CH:27]=3)[O:21][C:17]=2[CH:16]=1

Participants

6

Reactant 1

HCID 59275665HCID 59275665, compound

Product 1

HCID 59275241HCID 59275241, compoundYield 96%

Reagents, catalysts & solvents 4

HCID 23925IronCatalystHCID 176Acetic AcidSolventHCID 702EthanolSolventHCID 8857Ethyl AcetateSolvent

Procedure

Iron (28 mg, 0.495 mmol) was added to a stirring solution of ethyl 5-(3-(tert-butoxycarbonyl)phenyl)-2-(4-fluorophenyl)-6-nitrobenzofuran-3-carboxylate (50 mg, 0.099 mmol) in EtOH (495 μL) and AcOH (495 μL) at 100° C. It was allowed to stir for 1 hr. The mixture was diluted with EtOAc and washed with 1M HCl, and sat NaCl. The organic phase was dried over Na2SO4, filtered and concentrated to give the titled compound (45 mg, 96%). 1H NMR (400 MHz, DMSO-d6) d ppm 7.99-8.06 (2 H, m), 7.89-7.96 (2 H, m), 7.65-7.72 (1 H, m), 7.61 (1 H, t, J=7.65 Hz), 7.55 (1 H, s), 7.31-7.40 (2 H, m), 7.00 (1 H, s), 5.10 (2 H, br. s.), 4.29 (2 H, q, J=7.03 Hz), 1.56 (9 H, s), 1.26 (3 H, t, J=7.15 Hz). LC-MS retention time: 2.03 min; m/z (MH+): parent does not ionize. 420 (-tBu) was observed. LC data was recorded on a Shimadzu LC-10AS liquid chromatograph equipped with a Waters XBridge 5 u C18 4.6×50 mm column using a SPD-10AV UV-V is detector at a detector wave length of 220 nM. The elution conditions employed a flow rate of 5 ml/min, a gradient of 100% solvent A/0% solvent B to 0% solvent A/100% solvent B, a gradient time of 2 min, a hold time of 1 min, and an analysis time of 3 min where solvent A was 5% acetonitrile/95% H2O/10 mM ammonium acetate and solvent B was 5% H2O/95% acetonitrile/10 mM ammonium acetate. MS data was determined using a Micromass Platform for LC in electrospray mode.

Workup

  1. washwashed with 1M HCl
  2. dry with materialThe organic phase was dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated

Sources & evidence

ORD record
ord-26d3e29cfb204405b773fba4c6f6de6d
Source dataset
uspto-grants-2014_05
Patent number
US08722688B2

Reaction notes

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