Quinoline → HCID 53913170, compound

HRID 2248352Notes

Reaction equation

HRID 2248352 reaction equation
[N:1]1([CH:6]([C:10]2[CH:19]=[CH:18][C:13]3[N:14]([CH3:17])[N:15]=[N:16][C:12]=3[CH:11]=2)[C:7]#[C:8][CH3:9])[CH:5]=[CH:4][N:3]=[CH:2]1.N1C2C(=CC=CC=2)C=CC=1.C(OCC)(=O)C.[H][H]>[Pd].C(O)C>[N:1]1([CH:6]([C:10]2[CH:19]=[CH:18][C:13]3[N:14]([CH3:17])[N:15]=[N:16][C:12]=3[CH:11]=2)[CH:7]=[CH:8][CH3:9])[CH:5]=[CH:4][N:3]=[CH:2]1

Participants

7

Procedure

A mixture of 7 parts of 5-[1(1H-imidazol-1-yl)-2-butynyl]-1-methyl-1H-benzotriazole, 0.1 parts of quinoline, 54 parts of ethyl acetate and 32 parts of ethanol was hydrogenated at 931.00 Pa and at room temperature with 0.3 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off over diatomaceous earth and the filtrate was evaporated. The residue was purified by column chromatography over silica gel using a mixture of dichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of dichloromethane and 1,1'-oxybisethane. The product was filtered off and dried, yielding 1.4 parts (19.7%) of 5-[1-(1H-imidazol-1-yl)-2-butenyl]-1-methyl-1H-benzotriazole; mp. 104° C. (compound 240).

Workup

  1. filtrationthe catalyst was filtered off over diatomaceous earth
  2. customthe filtrate was evaporated
  3. customThe residue was purified by column chromatography over silica gel using
  4. additiona mixture of dichloromethane and methanol (95:5 by volume) as eluent
  5. customThe pure fractions were collected
  6. customthe eluent was evaporated
  7. customThe residue was crystallized from a mixture of dichloromethane and 1,1'-oxybisethane
  8. filtrationThe product was filtered off
  9. customdried

Sources & evidence

ORD record
ord-d06e96acf02f42d49f69a919a650c365
Source dataset
uspto-grants-1991_08
Patent number
US05039677

Reaction notes

Loading…