HCID 57426205, compound → HCID 57426206, compound

HRID 2426207Notes

Reaction equation

HRID 2426207 reaction equation
[C:1]([O:5][C:6](=[O:28])[CH2:7][N:8]1[C:16]2[C:11](=[C:12]([N+:17]([O-])=O)[CH:13]=[CH:14][CH:15]=2)[CH:10]([CH2:20][CH2:21][CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH2:9]1)([CH3:4])([CH3:3])[CH3:2]>CCO.[Pd]>[NH2:17][C:12]1[CH:13]=[CH:14][CH:15]=[C:16]2[C:11]=1[CH:10]([CH2:20][CH2:21][CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24])[CH2:9][N:8]2[CH2:7][C:6]([O:5][C:1]([CH3:3])([CH3:4])[CH3:2])=[O:28]

Participants

4

Reactant 1

HCID 57426205HCID 57426205, compound

Product 1

HCID 57426206HCID 57426206, compound

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

A mixture of ethyl 4-[1-(2-tert-butoxy-2-oxoethyl)-4-nitro-2,3-dihydro-1H-indol-3-yl]butanoate from Step C (1.10 g, 2.80 mmol) and 10% Pd/C (150 mg) in EtOH (50 mL) was stirred under an atmosphere of hydrogen (ca. 1 atm). After 18 b, the reaction was filtered through a Celite pad and concentrated in vacuo to give the title compound. MS: m/z/z 363 (M+1).

Workup

  1. filtrationAfter 18 b, the reaction was filtered through a Celite pad
  2. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-7e4d9ca565d44c75afcfbcdc439010b1
Source dataset
uspto-grants-2011_06
Patent number
US07968540B2

Reaction notes

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