3,4-dihydro-2H-pyran → HCID 57861278, compound

HRID 1518067Notes

Reaction equation

HRID 1518067 reaction equation
[F:1][C:2]([F:24])([F:23])[C:3]1[CH:4]=[C:5]([CH:16]=[C:17]([C:19]([F:22])([F:21])[F:20])[CH:18]=1)[CH2:6][NH:7][C:8]1[N:9]=[N:10][N:11]([CH2:13][CH2:14][OH:15])[N:12]=1.[O:25]1[CH:30]=[CH:29][CH2:28][CH2:27][CH2:26]1.C1(C)C=CC(S([O-])(=O)=O)=CC=1.[NH+]1C=CC=CC=1>C(Cl)Cl>[F:20][C:19]([F:21])([F:22])[C:17]1[CH:16]=[C:5]([CH:4]=[C:3]([C:2]([F:1])([F:23])[F:24])[CH:18]=1)[CH2:6][NH:7][C:8]1[N:9]=[N:10][N:11]([CH2:13][CH2:14][O:15][CH:26]2[CH2:27][CH2:28][CH2:29][CH2:30][O:25]2)[N:12]=1

Participants

5

Procedure

A mixture of 2-(5-{N-[3,5-bis(trifluoromethyl)benzyl]amino}tetrazol-2-yl)ethanol (0.68 g, 1.9 mmol), 3,4-dihydro-2H-pyran (DHP, 0.35 g, 4.2 mmol) and a catalytic amount of pyridinium p-toluene sulfonate (PPTS, 0.050 g, 0.20 mmol) in CH2Cl2 (10 mL) is stirred at room temperature for 10 hours. The resulting mixture is quenched by addition of sat. NaHCO3 aq. and extracted with EtOAc. The organic layer is washed with brine, dried over magnesium sulfate, filtered and concentrated. The crude product is purified by silica gel column chromatography to give N-[3,5-bis(trifluoromethyl)benzyl]-N-{2-[2-(tetrahydropyran-2-yloxy)ethyl]-2H-tetrazol-5-yl}amine.

Workup

  1. customThe resulting mixture is quenched by addition of sat. NaHCO3 aq.
  2. extractionextracted with EtOAc
  3. washThe organic layer is washed with brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe crude product is purified by silica gel column chromatography

Sources & evidence

ORD record
ord-7f8de93e78ff4b89b48e9dce709db6a3
Source dataset
uspto-grants-2012_07
Patent number
US08232403B2

Reaction notes

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