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HRID 916723作成日:2026年10月27日

Hydrochloric Acid → 5-((4-((2-Carboxyethyl)carbamoyl)phenyl)diazenyl)-2-hydroxybenzoic acid

https://huagongshe.com/reaction/916723

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Salicylic AcidHCID 338—
反応物Methanesulfonic AcidHCID 6395—
反応物Sodium CarbonateHCID 10340—
反応物Sodium HydroxideHCID 14798—
反応物N-(4-Aminobenzoyl)-beta-alanineHCID 719629—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
生成物5-((4-((2-Carboxyethyl)carbamoyl)phenyl)diazenyl)-2-hydroxybenzoic acidHCID 5458590%

反応条件

温度10 °C

反応手順

N-(4-Aminobenzoyl)-β-alanine (100 g) was suspended in water (1300 mL) and methanesulfonic acid (115.4 g) was added to this mixture. The mixture was cooled to 10° C. and a solution of sodium nitrite (34.46 g) in water (200 mL) was added at a rate such that the temperature stayed below 12° C. The mixture was stirred for 30 min and added to an ice-cold solution of salicylic acid (69.65 g), sodium hydroxide (40.35 g) and sodium carbonate (106.9 g) in 1 L water at 7-12° C. After 3 hours at 10° C., the mixture was heated to 60-65° C. and acidified to pH 4.0-4.5 by the addition of hydrochloric acid. After a further 3 hours at 60-65° C., the mixture was cooled to ambient temperature, filtered, washed with water and dried in vacuo to yield Balsalazide. Yield ca. 90%. Balsalazide was transformed into its disodium salt in ca. 85% yield by treatment with aqueous NaOH solution followed by crystallization from n-propanol/methanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07271253B1
出典データセットuspto-grants-2007_09
ORD IDord-01acf431bb1044b4897a34e596b18957
出典メモuspto-grants-2007_09