Thiophene → HCID 70360090, compound

HRID 1650995Notes

Reaction equation

HRID 1650995 reaction equation
[CH2:1]1[CH:5]2[C:6](=O)[C:7]3[CH:8]=[CH:9][CH:10]=[CH:11][C:12]=3[CH:4]2[CH2:3][CH2:2]1.Cl.[CH3:15][NH:16][CH2:17][C:18]([OH:20])=[O:19].S1C=CC=C1.C([O-])(=O)C.[K+].[H][H]>CO.[Pd]>[CH3:15][N:16]([CH:6]1[C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][C:12]=2[CH:4]2[CH2:3][CH2:2][CH2:1][CH:5]12)[CH2:17][C:18]([OH:20])=[O:19]

Participants

8

Procedure

A mixture of 23.4 parts of 2,3,3a,8a-tetrahydrocyclopent[a]inden-8(1H)-one, 31.4 parts of methyl glycine hydrochloride, 1 part of a solution of thiophene in methanol 4%, 400 parts of methanol and 13.3 parts of potassium acetate was hydrogenated at normal pressure and at room temperature with 2.0 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in water and the product was extracted with dichloromethane. The extract was washed with a hydrochloric acid solution and a sodium hydroxide solution, dried, filtered and evaporated, yielding 29.0 parts (86.9%) of methyl N-(1,2,3,3a,8,8a-hexahydrocyclopent[a]inden-8yl)glycine as a residue (int. 3).

Workup

  1. filtrationthe catalyst was filtered off
  2. customthe filtrate was evaporated
  3. extractionthe product was extracted with dichloromethane
  4. washThe extract was washed with a hydrochloric acid solution
  5. dry with materiala sodium hydroxide solution, dried
  6. filtrationfiltered
  7. customevaporated

Sources & evidence

ORD record
ord-f1be4b6f5b85437c97c8b22901c67954
Source dataset
uspto-grants-1990_05
Patent number
US04927449

Reaction notes

Loading…