HCID 15486863, compound → HCID 10005184, compound

HRID 1954841Notes

Reaction equation

HRID 1954841 reaction equation
[Br:1][C:2]1[CH:25]=[C:24]([C:26]([CH3:28])=[CH2:27])[CH:23]=[C:22]([O:29][CH3:30])[C:3]=1[O:4][C:5]1[C:6]2[N:14]=[N:13][N:12]([CH:15]([CH2:19][CH2:20][CH3:21])[CH2:16][CH2:17][CH3:18])[C:7]=2[N:8]=[C:9]([CH3:11])[N:10]=1>C(O)C.[Pt]>[Br:1][C:2]1[CH:25]=[C:24]([CH:26]([CH3:28])[CH3:27])[CH:23]=[C:22]([O:29][CH3:30])[C:3]=1[O:4][C:5]1[C:6]2[N:14]=[N:13][N:12]([CH:15]([CH2:16][CH2:17][CH3:18])[CH2:19][CH2:20][CH3:21])[C:7]=2[N:8]=[C:9]([CH3:11])[N:10]=1

Participants

4

Procedure

Platinum black, 5% (0.19 g) was added to a solution of 7-[2-bromo-6-methoxy-4-(1-methylethenyl)phenoxy]-5-methyl-3-(1-propylbutyl)-3H-1,2,3-triazolo[4, 5-d]pyrimidine (0.17 g) in 50 mL of ethanol. The mixture was hydrogenated at a pressure of 40 psi for 18 hours and filtered through celite. The filtrate was stripped of the solvent under reduced pressure and the residue recrystallized from hexane to yield the title compound as a colorless crystalline solid, mp 129-131° C.

Workup

  1. filtrationfiltered through celite
  2. customthe residue recrystallized from hexane

Sources & evidence

ORD record
ord-037e683c1e5547ce9ee04b6af2ea9295
Source dataset
uspto-grants-2000_09
Patent number
US06124300

Reaction notes

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