Dimethyl Sulfoxide → 3-(1-(2-(6-methoxybenzofuran-3-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole

HRID 1767997Notes

Reaction equation

HRID 1767997 reaction equation
[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6]2[C:7]([CH2:10][CH2:11]I)=[CH:8][O:9][C:5]=2[CH:4]=1.N1CC=C([N:21]2[C:29]3[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=3)[CH:23]=[CH:22]2)CC1.C([N:33]([CH2:37][CH3:38])[CH:34]([CH3:36])C)(C)C.[CH3:39]S(C)=O>>[CH3:1][O:2][C:3]1[CH:14]=[CH:13][C:6]2[C:7]([CH2:10][CH2:11][N:33]3[CH2:34][CH:36]=[C:39]([C:23]4[C:24]5[C:29](=[CH:28][CH:27]=[CH:26][CH:25]=5)[NH:21][CH:22]=4)[CH2:38][CH2:37]3)=[CH:8][O:9][C:5]=2[CH:4]=1

Participants

5

Reactant 4

HCID 679Dimethyl SulfoxideHCID 81531DiisopropylethylamineHCID 23001082HCID 23001082, compoundHCID 236144453-(2-Iodoethyl)-6-methoxy-1-benzofuran

Product 1

HCID 112457323-(1-(2-(6-methoxybenzofuran-3-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-1H-indole

Procedure

A mixture of 2-(6-methoxy-1-benzofuran-3-yl)ethyl iodide (301 mg. 1 mmol) (obtained by the above mentioned process) and 3 (1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole (198 mg, 1 mmol) was heated at 120° C. in DMSO in the presence of N,N-diisopropylethylamine (5 ml, excess) for 24 hrs. At the end, the reaction mixture was quenched with water and extracted with chloroform. The organic layer was washed with water and dried over anhydrous MgSO4 and concentrated to dryness. The dark colored solid was purified by silica-gel column chromatography by eluting it with 70% ethyl acetae:hexane. 3-{1-[2-(6-methoxy-1-benzofuran-3-yl)ethyl]-1,2,3,6-tetrahydro-4-pyridinyl}-1H-indole was isolated as yellow oil; Yield: 180 mg (48%); 373 (M+H); 1H NMR: δ□8.6 (d, 1H), 8.25 (bs, 1H), 7.9 (d,1H), 7.6–6.9 (m, 7H), 6.23 (bs, 1H), 3.85 (s, 3H), 3.5 (m,2H), 3.0 (m, 2H), 2.8 (m, 4H), 2.65 (m, 2H).

Workup

  1. customobtained by the
  2. customAt the end, the reaction mixture was quenched with water
  3. extractionextracted with chloroform
  4. washThe organic layer was washed with water
  5. dry with materialdried over anhydrous MgSO4
  6. concentrationconcentrated to dryness
  7. customThe dark colored solid was purified by silica-gel column chromatography
  8. washby eluting it with 70% ethyl acetae

Sources & evidence

ORD record
ord-9d5b74a229e5486b84531b4883e643a6
Source dataset
uspto-grants-2007_06
Patent number
US07235569B2

Reaction notes

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