Water → HCID 86708641, compound

HRID 921760Notes

Reaction equation

HRID 921760 reaction equation
[C:1]([C:3]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N+:12]([O-])=O)[CH:10]=2)[N:5]([CH:15]2[CH2:20][CH2:19][N:18]([C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH2:17][CH2:16]2)[CH:4]=1)#[N:2].[Cl-].[NH4+].O>C(O)C.[Fe]>[NH2:12][C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][CH:8]=1)[N:5]([CH:15]1[CH2:20][CH2:19][N:18]([C:21]([O:23][C:24]([CH3:25])([CH3:27])[CH3:26])=[O:22])[CH2:17][CH2:16]1)[CH:4]=[C:3]2[C:1]#[N:2]

Participants

6

Reactant 3

HCID 962WaterHCID 25517Ammonium ChlorideHCID 86708640HCID 86708640, compound

Product 1

HCID 86708641HCID 86708641, compoundYield 21.4%

Reagents, catalysts & solvents 2

HCID 23925IronCatalystHCID 702EthanolSolvent

Conditions

Temperature
85 °C

Procedure

tert-butyl 4-(3-cyano-5-nitro-1H-indol-1-yl)piperidine-1-carboxylate (1.02 g, 2.75 mmol), Iron (0.923 g, 16.52 mmol), and ammonium chloride (1.031 g, 19.28 mmol) were suspended in a mixture of Ethanol (10 mL)/Water (10 mL). The reaction mixture was heated in oil bath at 85° C. for 20 min. The reaction mixture was filtered through Celite, and then washed with water, MeOH and EtOAc. The combined filtrates were concentrated to almost dryness, and then mixed with aq. NaHCO3 and EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and evaporated to dryness to give tert-butyl 4-(5-amino-3-cyano-1H-indol-1-yl)piperidine-1-carboxylate (200 mg).

Workup

  1. filtrationThe reaction mixture was filtered through Celite
  2. washwashed with water, MeOH and EtOAc
  3. concentrationThe combined filtrates were concentrated to almost dryness
  4. additionmixed with aq. NaHCO3 and EtOAc
  5. washThe organic layer was washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customevaporated to dryness

Sources & evidence

ORD record
ord-ccc0d80d95ea4566a7bb1b79b9551dfb
Source dataset
uspto-grants-2016_03
Patent number
US09273057B2

Reaction notes

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