Methyl iodide → HCID 86585351, compound

HRID 1370413Notes

Reaction equation

HRID 1370413 reaction equation
[CH3:1][O:2][C:3](=[O:24])[CH:4]([C:9]1[NH:10][C:11]2[C:16]([C:17]=1[CH2:18][CH2:19][N:20]=[N+:21]=[N-:22])=[C:15]([Cl:23])[CH:14]=[CH:13][CH:12]=2)[C:5]([O:7][CH3:8])=[O:6].[CH3:25][O-].[Na+].CI>CO>[CH3:1][O:2][C:3](=[O:24])[C:4]([C:9]1[NH:10][C:11]2[C:16]([C:17]=1[CH2:18][CH2:19][N:20]=[N+:21]=[N-:22])=[C:15]([Cl:23])[CH:14]=[CH:13][CH:12]=2)([CH3:25])[C:5]([O:7][CH3:8])=[O:6]

Participants

5

Procedure

To a solution of 2-[3-(2-azidoethyl)-4-chloro-1H-indol-2-yl]-propanedioic acid dimethyl ester (19.3 mmol) in dry MeOH (0.1 L) at 0° C. under argon was added a 25% NaOMe in MeOH (4.37 mL, 19.11 mmol). The reaction mixture was stirred for 30 min, and MeI (1.82 mL, 29.2 mmol) was added. The mixture was stirred briefly at rt, and then was refluxed overnight. The reaction mixture was concentrated. The residue was taken up with cold H2O. This mixture was extracted with Et2O. The combined Et2O extracts were washed with H2O, dried, filtered, and concentrated to an oil. This oil was purified by silica chromatography to give the title compound: TLC Rf=0.50 (CH2Cl2), MS (ESI+) 387.0; 1H NMR (300 MHz CDCl3) δ 9.95 (1H), 7.27 (1H), 7.07 (2H), 3.83 (6H), 3.48 (2H), 3.15 (2H), 1.94 (3H).

Workup

  1. stirringThe mixture was stirred briefly at rt
  2. temperaturewas refluxed overnight
  3. concentrationThe reaction mixture was concentrated
  4. extractionThis mixture was extracted with Et2O
  5. washThe combined Et2O extracts were washed with H2O
  6. customdried
  7. filtrationfiltered
  8. concentrationconcentrated to an oil
  9. customThis oil was purified by silica chromatography

Sources & evidence

ORD record
ord-5c5c8a706c3d481d9e301518222f129e
Source dataset
uspto-grants-2003_06
Patent number
US06583135B2

Reaction notes

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