ChemicalBook--->CAS DataBase List--->158465-13-5

158465-13-5

158465-13-5 Structure

158465-13-5 Structure
IdentificationBack Directory
[Name]

2-Benzothiazolamine,5,7-dichloro-(9CI)
[CAS]

158465-13-5
[Synonyms]

5,7-Dichloro-2-benzothiazolamine
2-BenzothiazolaMine, 5,7-dichloro-
5,7-Dichloro-benzothiazol-2-ylamine
5,7-dichloro-1,3-benzothiazol-2-amine
2-Benzothiazolamine,5,7-dichloro-(9CI)
[EINECS(EC#)]

200-258-5
[Molecular Formula]

C7H4Cl2N2S
[MDL Number]

MFCD10693482
[MOL File]

158465-13-5.mol
[Molecular Weight]

219.09
Chemical PropertiesBack Directory
[Boiling point ]

376.7±45.0 °C(Predicted)
[density ]

1.654
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

2.17±0.30(Predicted)
Safety DataBack Directory
[HS Code ]

29342000
Hazard InformationBack Directory
[Chemical Properties]

White solid
[Synthesis]

3,5-DICHLOROPHENYLTHIOUREA

107707-33-5

2-Benzothiazolamine,5,7-dichloro-(9CI)

158465-13-5

Bromine (1.2 g, 7.4 mmol) was added slowly and dropwise to a solution of N-(3,5-dichlorophenyl)thiourea (1.0 g, 3.7 mmol) in chloroform (20 mL) at 0 °C. The reaction mixture was stirred at 60 °C for 10 h. The reaction was subsequently cooled to room temperature and the precipitated solid was collected by filtration. The solid was washed with acetone (4 x 5 mL) to remove unreacted bromine and by-products. The washed solid was dissolved in water (45 mL) and stirred at 95 °C for 30 min. Subsequently, the pH of the reaction solution was adjusted to 9 with 0.5 M sodium hydroxide solution. the precipitated solid was again collected by filtration and dried under vacuum to give 5,7-chlorobenzo[d]thiazol-2-amine (0.68 g, 81% yield) as a violet-gray solid.1H-NMR (CDCl3, 400 MHz) data were as follows: δ 7.43 (d, J = 1.6 Hz, 1H), δ 7.15 (d, J = 1.6Hz, 1H), 5.32 (broad peak, 2H).

[References]

[1] Patent: WO2017/69980, 2017, A1. Location in patent: Paragraph 00329; 00330
[2] Farmaco, 1998, vol. 53, # 12, p. 752 - 757
[3] Patent: TW2016/5805, 2016, A. Location in patent: Paragraph 0372; 0373
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