Sodium Bicarbonate → 6-Chloro-4-iodopyridin-3-ol

HRID 1438373Notes

Reaction equation

HRID 1438373 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([I:8])[C:5]([O:9]COC)=[CH:4][N:3]=1.C(=O)(O)[O-].[Na+]>C1COCC1.Cl>[Cl:1][C:2]1[N:3]=[CH:4][C:5]([OH:9])=[C:6]([I:8])[CH:7]=1

Participants

5

Conditions

Temperature
60 °C

Procedure

2-Chloro-4-iodo-5-methoxymethoxy-pyridine (0.8 g, 2.7 mmol) was dissolved in THF (4 mL) and 3N HCl (6 mL). The mixture was heated to 60° C. with magnetic stirring. Heating was maintained for 3 hours. The mixture was cooled to room temperature and the pH was adjusted to 7 with the slow addition of saturated aqueous sodium bicarbonate. The result was extracted with EtOAc (3×50 mL) dried over Na2SO4, filtered and concentrated. The solid was suspended in EtOAc and stirred for 12 hours at room temperature. The mixture was filtered and the filtrate was concentrated to yield an off white solid (0.63 g, 93%). 1H NMR (400 MHz, DMSO-d6): 611.10 (br s, 1H), 7.89 (s, 2H).

Workup

  1. temperatureHeating
  2. temperaturewas maintained for 3 hours
  3. temperatureThe mixture was cooled to room temperature
  4. extractionThe result was extracted with EtOAc (3×50 mL)
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. filtrationThe mixture was filtered
  9. concentrationthe filtrate was concentrated

Sources & evidence

ORD record
ord-088a40f3ddff438fb91892e1121c6550
Source dataset
uspto-grants-2009_11
Patent number
US07622605B2

Reaction notes

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