ChemicalBook--->CAS DataBase List--->719282-11-8

719282-11-8

719282-11-8 Structure

719282-11-8 Structure
IdentificationBack Directory
[Name]

CHEMBRDG-BB 9070752
[CAS]

719282-11-8
[Synonyms]

AKOS BC-3333
CHEMBRDG-BB 9070752
5-ACETAMIDO-2-CHLOROBENZOIC ACID
2-Chloro-5-(acetylamino)benzoic acid
5-(Acetylamino)-2-Chlorobenzoic Acid
Benzoic acid, 5-(acetylamino)-2-chloro-
5-(acetylamino)-2-chlorobenzoic acid(SALTDATA: FREE)
[Molecular Formula]

C9H8ClNO3
[MDL Number]

MFCD00466845
[MOL File]

719282-11-8.mol
[Molecular Weight]

213.62
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Brown to black Solid
Hazard InformationBack Directory
[Uses]

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

5-Amino-2-chlorobenzoic acid

89-54-3

Acetyl chloride

75-36-5

CHEMBRDG-BB 9070752

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
Spectrum DetailBack Directory
[Spectrum Detail]

CHEMBRDG-BB 9070752(719282-11-8)1HNMR
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