Sodium Iodide → 1-(2-Amino-4,6-dichloropyrimidin-5-yl)-3-buten-1-ol

HRID 882969

Reaction equation

HRID 882969 reaction equation
[In].[NH2:2][C:3]1[N:8]=[C:7]([Cl:9])[C:6]([CH:10]=[O:11])=[C:5]([Cl:12])[N:4]=1.[I-].[Na+].[CH2:15](Br)[CH:16]=[CH2:17]>[Zn].CN(C)C=O>[NH2:2][C:3]1[N:4]=[C:5]([Cl:12])[C:6]([CH:10]([OH:11])[CH2:17][CH:16]=[CH2:15])=[C:7]([Cl:9])[N:8]=1

Participants

7

Procedure

Indium powder (0.23 g) and zinc powder (1.31 g) were added to a mixture composed of commercially available 2-amino-4,6-dichloropyrimidine-5-carboaldehyde (1.92 g) and N,N-dimethylformamide (20 ml). Thereafter, sodium iodide (0.15 g) and allyl bromide (1.73 ml) were added to the mixture at room temperature. The resulting mixture was stirred for 3 hours. Thereafter, the reaction mixture was filtered through celite, and ethyl acetate was then added to the filtrate. The resulting mixture was successively washed with 1 N hydrochloric acid and a saturated saline in this order. The organic layer was dried over anhydrous sodium sulfate, and was then concentrated. Thereafter, hexane was added to the residue, and a precipitate was then collected by filtration, so as to obtain the above title compound (1.75 g) as a solid.

Workup

  1. filtrationThereafter, the reaction mixture was filtered through celite, and ethyl acetate
  2. additionwas then added to the filtrate
  3. washThe resulting mixture was successively washed with 1 N hydrochloric acid
  4. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  5. concentrationwas then concentrated
  6. additionThereafter, hexane was added to the residue
  7. filtrationa precipitate was then collected by filtration

Sources & evidence

ORD record
ord-8a2e9076b13c4b17a33388d5e1205058
Source dataset
uspto-grants-2012_08
Patent number
US08236813B2

Linked notes

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