Hydrochloric Acid → HCID 74088770, compound

HRID 1284583Notes

Reaction equation

HRID 1284583 reaction equation
[CH2:1]([O:4][N:5]=[C:6]([C:11]1[N:15]=[C:14]([NH:16][P:17]([O:21][CH3:22])([O:19][CH3:20])=[O:18])[S:13][N:12]=1)[C:7]([O:9]C)=[O:8])[CH:2]=[CH2:3].[OH-].[Na+:24].Cl>O1CCCC1>[CH2:1]([O:4][N:5]=[C:6]([C:11]1[N:15]=[C:14]([NH:16][P:17]([O:19][CH3:20])([O:21][CH3:22])=[O:18])[S:13][N:12]=1)[C:7]([O-:9])=[O:8])[CH:2]=[CH2:3].[Na+:24]

Participants

5

Procedure

To a solution of methyl 2-allyloxyimino-2-(5-dimethoxyphosphorylamino-1,2,4-thiadiazol-3-yl)acetate (syn isomer) (37.3 g) in tetrahydrofuran (106 ml) was added 1N-aqueous sodium hydroxide (234 ml) and the mixture was stirred for 2 hours at ambient temperature. The reaction mixture was adjusted to pH 5 with 6N hydrochloric acid and washed with ethyl acetate. The aqueous layer was separated out, adjusted to pH 1.0 with 6N hydrochloric acid and extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate and evaporated. The residue dissolved in methanol (50 ml) was added dropwise to a solution of sodium acetate (8.7 g) in methanol (90 ml) at ambient temperature under stirring, which was continued for one hour at the same temperature. To the mixture was added ethyl acetate (200 ml) and the resulting precipitate was collected by filtration, washed with ethyl acetate and dried to give sodium 2-allyloxyimino-2-(5-dimethoxyphosphorylamino-1,2,4-thiadiazol-3-yl)acetate (syn isomer) (32.6 g), mp. 168° to 173° C. (dec).

Workup

  1. washwashed with ethyl acetate
  2. customThe aqueous layer was separated out
  3. extractionextracted with ethyl acetate
  4. washThe extract was washed with brine
  5. dry with materialdried over magnesium sulfate
  6. customevaporated
  7. dissolutionThe residue dissolved in methanol (50 ml)
  8. additionwas added dropwise to a solution of sodium acetate (8.7 g) in methanol (90 ml) at ambient temperature
  9. stirringunder stirring
  10. waitwhich was continued for one hour at the same temperature
  11. additionTo the mixture was added ethyl acetate (200 ml)
  12. filtrationthe resulting precipitate was collected by filtration
  13. washwashed with ethyl acetate
  14. customdried

Sources & evidence

ORD record
ord-d236bd4622ca47f3a4971495751f4a59
Source dataset
uspto-grants-1986_01
Patent number
US04563449

Reaction notes

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