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3-METHYL-2-[(PHENYLSULFONYL)AMINO]BUTANOIC ACID synthesis

5synthesis methods
-

Yield:85849-94-1 99.68%

Reaction Conditions:

with sodium carbonate in water; for 5 h;

Steps:

2.2 General procedure for the synthesis of substituted benzenesulphonamoyl alkanamides (3a-p)

General procedure: Sodium carbonate (Na2CO3, 1.590g, 15mmol) was added to a solution of amino acids (2a-h, 12.5mmol) in water (15mL) with continuous stirring until all the solutes had dissolved. The solution was cooled to-5°C and the appropriate benzenesulphonyl chloride (1a-c, 15mmol) was added in four portions over a period of 1h. The slurry was further stirred at room temperature for about 4h. The progress of the reaction was monitored using TLC (MeOH/DCM, 1:9). Upon completion, the mixture was acidified using 20% aqueous hydrochloric acid to pH 2. The crystals was filtered via suction and washed with pH 2.2 buffer. The pure products (3a-x) were dried over self-indicating fused silica gel in a desiccator.

References:

Ugwu;Okoro;Ukoha;Okafor;Ibezim;Kumar [European Journal of Medicinal Chemistry,2017,vol. 135,p. 349 - 369]