2-Methylbenzenesulfonic acid → 1,2,4-Triazolo[3,4-f][1,6]naphthyridine, 9-phenyl-8-[4-[[4-[5-(2-pyridinyl)-1H-1,2,4-triazol-3-yl]-1-piperidinyl]methyl]phenyl]-

HRID 1678760Notes

Reaction equation

HRID 1678760 reaction equation
[C:1]1([C:7]2[C:8]([C:19]3[CH:24]=[CH:23][C:22]([CH2:25][N:26]4[CH2:31][CH2:30][CH:29]([C:32]5[NH:36][C:35]([C:37]6[CH:42]=[CH:41][CH:40]=[CH:39][N:38]=6)=[N:34][N:33]=5)[CH2:28][CH2:27]4)=[CH:21][CH:20]=3)=[N:9][C:10]3[C:15]([CH:16]=2)=[C:14]([NH:17][NH2:18])[N:13]=[CH:12][CH:11]=3)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:43](OOC)(OOC)OOC.C1(C)C(S(O)(=O)=O)=CC=CC=1>CO.C1(C)C=CC=CC=1>[C:1]1([C:7]2[C:8]([C:19]3[CH:20]=[CH:21][C:22]([CH2:25][N:26]4[CH2:27][CH2:28][CH:29]([C:32]5[NH:36][C:35]([C:37]6[CH:42]=[CH:41][CH:40]=[CH:39][N:38]=6)=[N:34][N:33]=5)[CH2:30][CH2:31]4)=[CH:23][CH:24]=3)=[N:9][C:10]3[CH:11]=[CH:12][N:13]4[CH:43]=[N:18][N:17]=[C:14]4[C:15]=3[CH:16]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

6

Procedure

To a solution of 8-9 (4.5 g, 8.1 mmol) in 20 mL methanol and 60 mL toluene was added trimethoxy orthoformate (3.5 g, 32.5 mmol) and toluenesulfonic acid (0.1 g, 0.8 mmol). The mixture was refluxed for 10 hrs. Upon removal of the solvent, the residue was purified by flash column chromatography (100% CHCl3 to 50% CHCl3 and 50% methanol) to afford the desired product 8-10.

Workup

  1. temperatureThe mixture was refluxed for 10 hrs
  2. customUpon removal of the solvent
  3. customthe residue was purified by flash column chromatography (100% CHCl3 to 50% CHCl3 and 50% methanol)

Sources & evidence

ORD record
ord-a308e9f9b8a64ca0b1874e50d2656307
Source dataset
uspto-grants-2011_08
Patent number
US08008317B2

Reaction notes

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