Water → 5-(Cyclohexyl-ethoxy-methyl)-2-(2,6-diethyl-phenyl)-4-ethoxy-pyridine

HRID 1392638Notes

Reaction equation

HRID 1392638 reaction equation
[H-].[Na+].[CH:3]1([CH:9]([C:11]2[CH:12]=[N:13][C:14]([C:20]3[C:25]([CH2:26][CH3:27])=[CH:24][CH:23]=[CH:22][C:21]=3[CH2:28][CH3:29])=[CH:15][C:16]=2[O:17][CH2:18][CH3:19])[OH:10])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1.I[CH2:31][CH3:32].O>CN(C=O)C>[CH:3]1([CH:9]([O:10][CH2:31][CH3:32])[C:11]2[C:16]([O:17][CH2:18][CH3:19])=[CH:15][C:14]([C:20]3[C:25]([CH2:26][CH3:27])=[CH:24][CH:23]=[CH:22][C:21]=3[CH2:28][CH3:29])=[N:13][CH:12]=2)[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1

Participants

6

Procedure

Sodium hydride (60% in mineral oil, 12 mg, 0.3 mmol) is added to a solution of cyclohexyl-[6-(2,6-diethyl-phenyl)-4-ethoxy-pyridin-3-yl]-methanol (74 mg, 0.2 mmol) in DMF (0.5 mL) at room temperature. The resulting mixture is stirred for 30 minutes. Iodoethane (31 mg, 0.2 mmol) is then added and the mixture is stirred for an additional 1 hour. Water (1 mL) is added to the above mixture and the aqueous layer is extracted with ethyl acetate (2×2 mL). The combined organic layers are dried and concentrated in vacuo. The crude product is purified with PTLC (hexanes/ethyl acetate 6:1) to give 5-(cyclohexyl-ethoxy-methyl)-2-(2,6-diethyl-phenyl)-4-ethoxy-pyridine. 1H NMR: (CDCl3) 8.50 (s, 1H), 7.28 (t, 1H), 7.12 (d, 2H), 6.70 (S, 1H), 4.45 (d, 1H), 4.03 (q, 2H), 3.34 (m, 2H), 2.34 (m, 4H), 2.02 (br, 1H), 1.73 (m, 4H), 1.21 (m, 4H), 1.05 (m, 13H).

Workup

  1. stirringthe mixture is stirred for an additional 1 hour
  2. extractionthe aqueous layer is extracted with ethyl acetate (2×2 mL)
  3. customThe combined organic layers are dried
  4. concentrationconcentrated in vacuo
  5. customThe crude product is purified with PTLC (hexanes/ethyl acetate 6:1)

Sources & evidence

ORD record
ord-e17738dcc580479093a2e8129e03bbc1
Source dataset
uspto-grants-2008_03
Patent number
US07342115B2

Reaction notes

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