Basic information Safety Supplier Related

CHEMBRDG-BB 9070752

Basic information Safety Supplier Related

CHEMBRDG-BB 9070752 Basic information

Product Name:
CHEMBRDG-BB 9070752
Synonyms:
  • CHEMBRDG-BB 9070752
  • 5-(Acetylamino)-2-Chlorobenzoic Acid
  • 5-ACETAMIDO-2-CHLOROBENZOIC ACID
  • AKOS BC-3333
  • 5-(acetylamino)-2-chlorobenzoic acid(SALTDATA: FREE)
  • Benzoic acid, 5-(acetylamino)-2-chloro-
  • 2-Chloro-5-(acetylamino)benzoic acid
CAS:
719282-11-8
MF:
C9H8ClNO3
MW:
213.62
Mol File:
719282-11-8.mol
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CHEMBRDG-BB 9070752 Chemical Properties

storage temp. 
Sealed in dry,Room Temperature
Appearance
Brown to black Solid
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CHEMBRDG-BB 9070752 Usage And Synthesis

Uses

5-Acetamido-2-chlorobenzoic Acid is used for preparation of 2-amino-5-substituted pyrimidine kinase inhibitors and use in therapy.

Synthesis

89-54-3

75-36-5

719282-11-8

1. In a dry reaction flask, 5-amino-2-chlorobenzoic acid (0.50 g, 2.9 mmol) was dissolved in dichloromethane (15 mL). 2. Acetyl chloride (0.30 mL, 4.2 mmol) and triethylamine (1.2 mL, 8.6 mmol) were added sequentially to the above solution. 3. The reaction mixture was stirred at room temperature for 2 h. When the reaction was complete, the mixture was slowly poured into water. 4. The aqueous phase was extracted with ethyl acetate and the organic layers were combined. 5. The combined organic layers were washed sequentially with water and saturated saline. 6. 6. The organic layer was dried over anhydrous sodium sulfate and filtered to remove the desiccant. 7. The filtrate was concentrated under pressure to give 5-(acetylamino)-2-chlorobenzoic acid (0.17 g, 27% yield) as a brown solid.

References

[1] Patent: WO2008/8234, 2008, A1. Location in patent: Page/Page column 115

CHEMBRDG-BB 9070752Supplier

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