HCID 19003088, compound → HCID 19003097, compound

HRID 488092Notes

Reaction equation

HRID 488092 reaction equation
[CH3:1][N:2]1[C:10]2[CH:9]=[CH:8][C:7]([OH:11])=[CH:6][C:5]=2[CH:4]2[CH2:12][CH2:13][CH:14]([NH:15]CC3C=CC=CC=3)[CH:3]12>C(O)C.[OH-].[OH-].[Pd+2]>[NH2:15][CH:14]1[CH:3]2[N:2]([CH3:1])[C:10]3[CH:9]=[CH:8][C:7]([OH:11])=[CH:6][C:5]=3[CH:4]2[CH2:12][CH2:13]1

Participants

4

Reactant 1

HCID 19003088HCID 19003088, compound

Product 1

HCID 19003097HCID 19003097, compoundYield 110.1%

Reagents, catalysts & solvents 2

HCID 9942167Palladium hydroxideCatalystHCID 702EthanolSolvent

Procedure

20% Palladium hydroxide on carbon (1.4 g) was added to a solution of 1,2,3,3a,4,8b-hexahydro-4-methyl-3-phenylmethylaminocyclopent[b]-indol-7-ol (14 grams) in ethanol (100 ml) and the mixture was hydrogenated at 45 psi H2 pressure using a Parr apparatus at 500° C. for 5 hours. The mixture was filtered and the solution was concentrated to give 3-amino-1,2,3,3a,4,8b-hexahydro-4-methylcyclopent[b]indol-7-ol (10.7 grams).

Workup

  1. customat 500° C.
  2. customfor 5 hours
  3. filtrationThe mixture was filtered
  4. concentrationthe solution was concentrated

Sources & evidence

ORD record
ord-dc7949b7f0ea47c5bd869fd04b2f4456
Source dataset
uspto-grants-1994_03
Patent number
US05298626

Reaction notes

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