HCID 22018328, compound → HCID 178466003, compound

HRID 392584Notes

Reaction equation

[CH2:1]([O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[CH:10]=[C:9]([C:14]([C:19]1[N:20]=[CH:21][N:22](C(C3C=CC=CC=3)(C3C=CC=CC=3)C3C=CC=CC=3)[CH:23]=1)([OH:18])[CH:15]([CH3:17])[CH3:16])[CH:8]=[CH:7]2)[CH3:2]>C(O)(=O)C.[C].[Pd]>[CH2:1]([O:3][C:4]1[CH:5]=[C:6]2[C:11](=[CH:12][CH:13]=1)[CH:10]=[C:9]([C:14]([C:19]1[N:20]=[CH:21][NH:22][CH:23]=1)([OH:18])[CH:15]([CH3:17])[CH3:16])[CH:8]=[CH:7]2)[CH3:2]

Participants

Conditions

Temperature: 60 °C

Procedure

1-(6-Ethoxynaphthalen-2-yl)-1-(1-trityl-1H-imidazol-4-yl)-2-methyl-1-propanol (0.60 g) was dissolved in acetic acid (10 ml) and 10% palladium carbon (0.2 g) was added and the mixture was stirred at 50° C. for 2 h and at 60° C. for 3 h under a hydrogen atmosphere. The catalyst was filtered off and the filtrate was concentrated to dryness. Recrystallization from THF-ethyl acetate gave the title compound (0.21 g) as a colorless crystalline powder.

Workup

filtrationThe catalyst was filtered off
concentrationthe filtrate was concentrated to dryness
customRecrystallization from THF-ethyl acetate

Sources & evidence

ORD record: ord-c261a3552936472e9670ffeaec8f39bb
Source dataset: uspto-grants-2004_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06800778B1

Reaction notes

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