HCID 19846612, compound → HCID 178507978, compound

HRID 2351586Notes

Reaction equation

HRID 2351586 reaction equation
[NH2:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([NH:9][C:10]([NH:12][CH2:13][CH:14](OC)OC)=[S:11])=[CH:4][C:3]=1[F:19]>S(=O)(=O)(O)O.O>[NH2:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([N:9]2[CH:14]=[CH:13][N:12]=[C:10]2[SH:11])=[CH:4][C:3]=1[F:19]

Participants

4

Procedure

A solution of 4-amino-3,5-difluorophenyl isothiocyanate in trichloromethane is treated with an equimolar amount of aminoacetaldehyde dimethyl acetal. The solvent is evaporated, and the residue is recrystallized from ethanol to yield N-(4-amino-3,5-difluorophenyl)-N'-(β,β-dimethoxyethyl)thiourea. A suspension of this thiourea in concentrated sulfuric acid and water (1:4) was refluxed for three hours. The mixture then is cooled and the solid that forms is filtered, washed with water, and dried. Recrystallization from ethanol yields 1-(4'-amino-3',5'-difluorophenyl)imidazole-2-thiol.

Workup

  1. temperaturewas refluxed for three hours
  2. temperatureThe mixture then is cooled
  3. filtrationthe solid that forms is filtered
  4. washwashed with water
  5. customdried
  6. customRecrystallization from ethanol

Sources & evidence

ORD record
ord-988a8420208b45bdb6f4e74eb5775b0f
Source dataset
uspto-grants-1989_10
Patent number
US04873357

Reaction notes

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