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Thionyl Chloride → 4-Bromothiazole-2-carbohydrazide

HRID 1423334
Notes
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Reaction equation

HRID 1423334 reaction equation
[Br:1][C:2]1[N:3]=[C:4]([C:7]([OH:9])=O)[S:5][CH:6]=1.S(Cl)(Cl)=O.O.[NH2:15][NH2:16]>CO>[Br:1][C:2]1[N:3]=[C:4]([C:7]([NH:15][NH2:16])=[O:9])[S:5][CH:6]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 24386Thionyl ChlorideHCID 24654Hydrazine hydrate (1:1)HCID 151220654-Bromo-1,3-thiazole-2-carboxylic acid

Product 1

HCID 580356604-Bromothiazole-2-carbohydrazideYield 78.1%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a solution of 4-bromothiazole-2-carboxylic acid (2.0 g, 9.8 mmol) in methanol (10 mL) was added thionyl chloride (710 μL, 9.8 mmol) and the mixture was refluxed for 3 hours. The solvent was removed under reduced pressure, and the residue was suspended in ethanol (10 mL). To this suspension was added hydrazine hydrate (2.4 mL, 49 mmol), and the reaction was heated to reflux for 90 minutes. The solvent was removed under reduced pressure, and the residue suspended in acetonitrile, filtered, and the solids were washed with acetonitrile, diethyl ether, and dried under vacuum to afford 1.7 g (77%) of 4-bromothiazole-2-carbohydrazide as a yellow solid. M+1=222.1

Workup

  1. temperaturethe mixture was refluxed for 3 hours
  2. customThe solvent was removed under reduced pressure
  3. temperaturethe reaction was heated
  4. temperatureto reflux for 90 minutes
  5. customThe solvent was removed under reduced pressure
  6. filtrationfiltered
  7. washthe solids were washed with acetonitrile, diethyl ether
  8. customdried under vacuum

Sources & evidence

ORD record
ord-d37f4317650e4463abaf8fd96d5acf43
Source dataset
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08927582B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes