Sodium Iodide → HCID 67338812, compound

HRID 1184538Notes

Reaction equation

HRID 1184538 reaction equation
C[Si](Cl)(C)C.[Cl:6][C:7]1[CH:8]=[C:9]([NH:13][C:14](/[CH:16]=[CH:17]/[C:18]2[CH:19]=[CH:20][C:21]([O:43][CH3:44])=[C:22]([O:24][P:25](=[O:42])([O:34]CC3C=CC=CC=3)[O:26]CC3C=CC=CC=3)[CH:23]=2)=[O:15])[CH:10]=[CH:11][CH:12]=1.[Na+:45].[I-].C[O-].[Na+]>CC#N.O>[P:25]([O-:42])([O-:34])([O:24][C:22]1[CH:23]=[C:18](/[CH:17]=[CH:16]/[C:14]([NH:13][C:9]2[CH:10]=[CH:11][CH:12]=[C:7]([Cl:6])[CH:8]=2)=[O:15])[CH:19]=[CH:20][C:21]=1[O:43][CH3:44])=[O:26].[Na+:45].[Na+:45]

Participants

7

Procedure

Trimethylsilylchloride (1.68 ml, 13.3 mmol) was added dropwise to a stirred solution of phosphoric acid dibenzyl ester 5-[(E)-2-(3-chloro-phenylcarbamoyl)-vinyl]-2-methoxy-phenyl ester (1.87 g, 3.32 mmol) and NaI (1.99 g, 13.3 mmol) in dry CH3CN (40 ml). The mixture was stirred for 1 h at RT and then diluted with water and extracted with AcOEt. The organic phase was dried over sodium sulphate and evaporated in vacuo. The crude was triturated with AcOEt and Et2O, filtered and dissolved in EtOH (100 ml). NaOMe (714 mg, 13.3 mmol) was added and the resulting mixture was stirred for 2 hrs at RT. The solvent was evaporated to dryness and the residue was crystallized from water to give the title sodium (E)-5-(3-(3-chlorophenylamino)-3-oxoprop-1-enyl)-2-methoxyphenyl phosphate (1.1 g).

Workup

  1. extractionextracted with AcOEt
  2. dry with materialThe organic phase was dried over sodium sulphate
  3. customevaporated in vacuo
  4. customThe crude was triturated with AcOEt and Et2O
  5. filtrationfiltered
  6. dissolutiondissolved in EtOH (100 ml)
  7. stirringthe resulting mixture was stirred for 2 hrs at RT
  8. customThe solvent was evaporated to dryness
  9. customthe residue was crystallized from water

Sources & evidence

ORD record
ord-328f3717ef1f47b591d952b1c15f24a2
Source dataset
uspto-grants-2014_03
Patent number
US08669261B2

Reaction notes

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