CHEMBRDG-BB 9070752
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
CHEMBRDG-BB 9070752 Chemical Properties
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- Brown to black Solid
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
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CHEMBRDG-BB 9070752(719282-11-8)Related Product Information
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- BUTAFENACIL
- CHEMBRDG-BB 9070752
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