Acetoxyacetyl chloride → (7-Mercapto[1,3]thiazolo[5,4-d]pyrimidin-2-yl)methanol

HRID 32588Notes

Reaction equation

HRID 32588 reaction equation
[NH2:1][C:2]1[C:3]([SH:9])=[N:4][CH:5]=[N:6][C:7]=1[SH:8].[C:10](OCC(Cl)=O)(=[O:12])[CH3:11]>N1C=CC=CC=1>[SH:8][C:7]1[C:2]2[N:1]=[C:11]([CH2:10][OH:12])[S:9][C:3]=2[N:4]=[CH:5][N:6]=1

Participants

4

Conditions

Temperature
115 °C

Procedure

A cooled (ice bath) suspension of 5-aminopyrimidine-4,6-dithiol (Intermediate 41) (40.0 g) in pyridine (500 mL) was stirred under an inert atmosphere atmosphere. Acetoxyacetyl chloride (38 mL) was added over 10 minutes, the ice bath was removed and the mixture stirred at ambient temperature overnight. The mixture was concentrated in vacuo and azeotroped three times with toluene (200 mL). The residue was suspended in 2N HCl, and heated at 115° C. for 5 hours, and allowed to cool to ambient temperature overnight. The resulting suspension was filtered, washed with water (200 mL) and ether (200 mL) to give the title compound as a pale brown solid (48.3 g, 97%) (containing 10% of (7-mercapto[1,3]thiazolo[5,4-d]pyrimidin-2-yl)methyl acetate);

Workup

  1. temperatureA cooled
  2. customthe ice bath was removed
  3. stirringthe mixture stirred at ambient temperature overnight
  4. concentrationThe mixture was concentrated in vacuo
  5. customazeotroped three times with toluene (200 mL)
  6. temperatureto cool to ambient temperature overnight
  7. filtrationThe resulting suspension was filtered
  8. washwashed with water (200 mL) and ether (200 mL)

Sources & evidence

ORD record
ord-7d12168941a74394a75a0b8745e7b7a3
Source dataset
uspto-grants-2008_09
Patent number
US07427616B2

Reaction notes

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