Chlorine → 7-Chloro-1,3-benzothiazol-6-amine

HRID 2300403Notes

Reaction equation

HRID 2300403 reaction equation
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]2[N:6]=[CH:7][S:8][C:4]=2[CH:3]=1.[Cl:11]Cl.CCOC(C)=O.CCCCCC>CC(O)=O.CCOC(C)=O>[Cl:11][C:3]1[C:4]2[S:8][CH:7]=[N:6][C:5]=2[CH:9]=[CH:10][C:2]=1[NH2:1]

Participants

6

Conditions

Temperature
25 °C

Procedure

To a solution of 6-aminobenzothiazole (2.0 g, 13.4 mmol) in 100 mL of AcOH was added a solution of Cl2 saturated AcOH and the resulting reaction mixture was stirred for 1 h at 25° C. Reaction mixture was concentrated in vacuo, yielding a yellow solid which was dissolved in EtOAc and washed with aq. NaHCO3. Organic layer was dried over Na2SO4 and concentrated in vacuo, yielding an oil which was subjected to column chromatography (10-50% EtOAc/n-Hexane) to obtain 7.8 g (34 mmol, 80%) of the desired product.

Workup

  1. customthe resulting reaction mixture
  2. customReaction mixture
  3. concentrationwas concentrated in vacuo
  4. customyielding a yellow solid which
  5. washwashed with aq. NaHCO3
  6. dry with materialOrganic layer was dried over Na2SO4
  7. concentrationconcentrated in vacuo
  8. customyielding an oil which

Sources & evidence

ORD record
ord-186fe76e1d5d4107b5680c36ba5a566d
Source dataset
uspto-grants-2002_12
Patent number
US06498177B2

Reaction notes

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