Acitazanolast CAS NO.114607-46-4

Product Name:    Acitazanolast
Synonyms:    2-(3-(1H-tetrazol-5-yl)phenylamino)-2-oxoacetic acid;Acitazanolast, >=98%;Acitazanolast.H2O;3-(1H-TETRAZOL-5-YL)-OXANILICACI;MTCC;N-[3-(1H-Tetrazol-5-yl)phenyl]oxamidic acid;Oxo[[3-(1H-tetrazol-5-yl)phenyl]amino]acetic acid;Oxo[3-(1H-tetrazole-5-yl)anilino]acetic acid
CAS:    114607-46-4
MF:    C9H7N5O3
MW:    233.18
EINECS:    
Product Categories:    
Mol File:    114607-46-4.mol

Melting point     241-243 °C (decomp)
density     1.660±0.06 g/cm3(Predicted)
pka    2.05±0.20(Predicted)
Safety Information
MSDS Information
Acitazanolast Usage And Synthesis
Originator    Zepelin ,Kowa
Manufacturing Process    2 Methods of preparation of 3-(1H-tetrazol-5-yl)oxanilic acid:
1. 5.0 g of 3-(1H-tetrazol-5-yl)aniline was dissolved in 25 ml of N,Ndimethylformamide, followed by adding 5.68 g of triethylamine. Then, 5.64 g of ether oxalyl chloride was dropwise added to the solution while cooling in ice water. After completion of the dropwise addition, the reaction temperature was slowly raised up to room temperature and the reaction was continued for 15 h. After the reaction was completed, the reaction mixture was poured into 100 ml of ice water and crystals separated out from the solution was filtered off to obtain 8.3 g of ethyl 3-(1H-tetrazol-5-yl)oxanilate (yield 94.1%), melting point 192°-l93°C (recrystallized from acetone/n-hexane).
The ethyl 3-(1H-tetrazol-5-yl)oxanilate (5.0 g), was dissolved in 35 ml of ethanol and 100 ml of 0.5 N sodium hydroxide was dropwise added thereto under water cooling. After the dropwise addition, the reaction temperature was slowly raised up to room temperature and under such condition, the reaction was carried out for 3 h. This solution was dropwise added to 70 ml of 4 N hydrochloric acid at room temperature. Thereafter, the solution was stirred for 1 h and crystals separated out from the solution was filtered off. The resultant crystals were washed with water and 3.9 g of 3-(1H-tetrazol-5- yl)oxanilic acid was recovered (yield 87.4%), melting point 241°-243°C (dec. recrystallized from isopropyl).
2. Oxalyl chloride (12.0 g) was dissolved in 50 ml of anhydrous dimethoxyethane. To this solution a solution of 3-(1H-tetrazol-5-yl)aniline (5.0 g) in 250 ml of anhydrous dimethoxyethane was dropwise added over 3 h at room temperature while stirring. Insolubles were removed by filtering the solution, then 50 ml of water was gradually added to the reaction mixture under ice cooling and stirring was continued for 1 h at room temperature. Then, 500 ml of ethyl acetate was added thereto to carry out extraction, the extract was washed with water, dried over anhydrous sodium sulfate and then the solvent was distilled off to obtain 5.4 g of the 3-(1H-tetrazol-5- yl)oxanilic acid (yield 74.8%), melting point 241°-243°C (dec. recrystallized from isopropyl).
Therapeutic Function    Anti-asthmatic, Antiallergic, Bronchodilator
Acitazanolast Preparation Products And Raw materials
Raw materials    Sodium hydroxide-->Oxalyl chloride-->Hydrochloric acid-->Triethylamine-->5-(3-AMINOPHENYL)TETRAZOLE