HCID 178418361, compound → HCID 178486573, compound

HRID 428619Notes

Reaction equation

HRID 428619 reaction equation
[NH:1]1[CH:5]=[C:4]([CH:6]2[C:14]3[C:9](=[C:10]([CH3:18])[C:11]([CH3:17])=[C:12]([O:15][CH3:16])[CH:13]=3)[CH:8](O)[CH2:7]2)[N:3]=[CH:2]1.[H][H]>C(O)C.Cl.[Pd]>[CH3:16][O:15][C:12]1[CH:13]=[C:14]2[C:9]([CH2:8][CH2:7][CH:6]2[C:4]2[N:3]=[CH:2][NH:1][CH:5]=2)=[C:10]([CH3:18])[C:11]=1[CH3:17]

Participants

6

Procedure

3-(1H-Imidazol-4-yl)-5-methoxy-6,7-dimethylindan-1-ol (0.29 g) is dissolved in the mixture of ethanol (30 ml) and concentrated hydrochloric acid (0.2 ml). The solution is hydrogenated at 50-55° C. with 10% palladium on carbon as catalyst until no more hydrogen is consumed. The mixture is filtered and the filtrate is evaporated to dryness. The residue is crystallized from the mixture of ethyl acetate and ethanol. M.p. of the hydrochloride salt is 174-177° C.

Workup

  1. customis consumed
  2. filtrationThe mixture is filtered
  3. customthe filtrate is evaporated to dryness
  4. customThe residue is crystallized from the mixture of ethyl acetate and ethanol
  5. customis 174-177° C.

Sources & evidence

ORD record
ord-53b654ec5e7b482bacf04cbc63324755
Source dataset
uspto-grants-2001_11
Patent number
US06313311B1

Reaction notes

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