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Bromine → 5-Bromo-1,3-benzothiazol-2-amine

HRID 984713
Notes
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Reaction equation

HRID 984713 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]([NH2:11])=[S:10])[CH:5]=[CH:6][CH:7]=1.BrBr>C(Cl)(Cl)Cl>[NH2:11][C:9]1[S:10][C:5]2[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][C:4]=2[N:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24408BromineHCID 2735619(3-Bromophenyl)thiourea

Product 1

HCID 137757855-Bromo-1,3-benzothiazol-2-amineYield 47.6%

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent2×

Procedure

A solution of Intermediate 62 (1.29 g) in chloroform (12 ml) was added dropwise with a solution of bromine (272 μl, WAKO) in chloroform (1.5 ml), refluxed with heating for 2.5 hours and then stirred at room temperature for 16 hours. The reaction mixture was concentrated under reduced pressure, neutralized with 5% aqueous ammonia and then added with water (50 ml) and methylene chloride (150 ml) for extraction. The organic layer was dried, and then the solvent was evaporated under reduced pressure. The residue was purified by column chromatography (Quad, hexane:ethyl acetate=2:1) to obtain the title compound (Intermediate 63, 609 mg).

Workup

  1. temperaturerefluxed
  2. temperaturewith heating for 2.5 hours
  3. concentrationThe reaction mixture was concentrated under reduced pressure
  4. additionadded with water (50 ml) and methylene chloride (150 ml) for extraction
  5. customThe organic layer was dried
  6. customthe solvent was evaporated under reduced pressure
  7. customThe residue was purified by column chromatography (Quad, hexane:ethyl acetate=2:1)

Sources & evidence

ORD record
ord-7ab3c645bb234779bf09289e3d7e8b0a
Source dataset
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06867320B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes