2-Amino-6-nitrobenzothiazole → 2,6-Benzothiazolediamine

HRID 130339

Reaction equation

HRID 130339 reaction equation
[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([N+:11]([O-])=O)[CH:8]=[CH:7][C:5]=2[N:6]=1.[H][H]>CO.[Pd]>[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([NH2:11])[CH:8]=[CH:7][C:5]=2[N:6]=1

Participants

5

Reactant 2

HCID 227042-Amino-6-nitrobenzothiazoleHCID 178418361HCID 178418361, compound

Product 1

HCID 215042,6-BenzothiazolediamineYield 99.3%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 887MethanolSolvent2×

Procedure

2-Amino-6-nitrobenzothiazole (500 mg, 2.56 mmol) was dissolved in methanol (20 mL) and 10% palladium on carbon (50 mg) was added as a slurry in methanol (1 mL). The atmosphere was replaced with hydrogen and the suspension was stirred overnight. The catalyst was removed by suction filtration and the solvent evaporated to afford 2,6-diaminobenzothiazole (420 mg, 99%) as a pale yellow solid.

Workup

  1. customThe catalyst was removed by suction filtration
  2. customthe solvent evaporated

Sources & evidence

ORD record
ord-2bb820c6c6b84c03b05572fcc80c66e2
Source dataset
uspto-grants-2008_06
Patent number
US07381734B2

Linked notes

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