Water → HCID 21251118, compound

HRID 1531908Notes

Reaction equation

HRID 1531908 reaction equation
O.C1(C)C=CC(S(O)(=O)=O)=CC=1.O.[C:14]([C:18]1[CH:23]=[C:22]([O:24][CH3:25])[N:21]=[C:20]([O:26][CH3:27])[C:19]=1[NH:28]C(=O)OC(C)(C)C)([O:16][CH3:17])=[O:15].C(=O)(O)[O-].[Na+]>C1(C)C=CC=CC=1>[NH2:28][C:19]1[C:20]([O:26][CH3:27])=[N:21][C:22]([O:24][CH3:25])=[CH:23][C:18]=1[C:14]([O:16][CH3:17])=[O:15]

Participants

6

Procedure

p-Toluene sulfonic acid hydrate (0.282 g, 1.48 mmol) was dissolved in toluene (11 mL) and heated to reflux overnight with azeotropic removal of water (Dean-Stark trap). The next day, the reaction was cooled to room temperature and the product of Example 21, dissolved in toluene (4 mL), was added. The reaction was heated back to reflux for 0.5 hours. The reaction was cooled to room temperature and poured into sodium bicarbonate (sat) and extracted 3 times with ether. The organics were combined, washed with brine, dried over MgSO4, concentrated in vacuo. The residue was purified by column chromatography using hexane/ethyl acetate as eluant (gradient 100% to 9/1) to provide 0.278 g (97%) of methyl 3-amino-2,6-dimethoxyisonicotinate as a yellow solid. Electrospray Mass Spec: 212.8 (M+H)+

Workup

  1. temperatureheated
  2. additionwas added
  3. temperatureThe reaction was heated back
  4. temperatureto reflux for 0.5 hours
  5. temperatureThe reaction was cooled to room temperature
  6. extractionextracted 3 times with ether
  7. washwashed with brine
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated in vacuo
  10. customThe residue was purified by column chromatography

Sources & evidence

ORD record
ord-478e5c2439844849881b833f8ac820ba
Source dataset
uspto-grants-2001_03
Patent number
US06200996B1

Reaction notes

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