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Bromine → 5,7-Difluorobenzo[d]thiazol-2-amine

HRID 30885
Notes
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Reaction equation

HRID 30885 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]([NH2:12])=[S:11])[CH:5]=[C:6]([F:8])[CH:7]=1.BrBr>ClCCCl>[F:1][C:2]1[CH:7]=[C:6]([F:8])[C:5]2[S:11][C:10]([NH2:12])=[N:9][C:4]=2[CH:3]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 24408BromineHCID 2783293(3,5-Difluorophenyl)thiourea

Product 1

HCID 150505645,7-Difluorobenzo[d]thiazol-2-amineYield 90.7%

Reagents, catalysts & solvents 1

HCID 111,2-DichloroethaneSolvent2×

Conditions

Temperature
10 °C

Procedure

To a suspension of N-(3,5-difluorophenyl) thiourea (3.40 g, 18.07 mmol) in DCE (95 mL) was added a solution of bromine in DCE (5 mL) below 30° C. The mixture was heated at reflux for 2.5 h, then cooled to 10° C., and the precipitate formed was collected by filtration and washed with DCE. The solid was stirred with water (200 mL), basified by treatment with conc. ammonium hydroxide, filtered, and dried in a vacuum oven to afford 5,7-difluoro-1,3-benzothiazol-2-amine (3.05 g, 90%). ret. time 2.18; m/z 187.1 (MH+); 1H NMR (400 MHz, DMSO-d6) δ 6.92 (m, 1H), 7.00 (m, 2H), 7.92 (s, 2H).

Workup

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 2.5 h
  3. customthe precipitate formed
  4. filtrationwas collected by filtration
  5. washwashed with DCE
  6. filtrationfiltered
  7. customdried in a vacuum oven

Sources & evidence

ORD record
ord-e05c5f3294924d8ab7c23eb1f3297773
Source dataset
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07423156B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes