Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A kind of method of synthesizing mesalamine

A technology of quality and nitrosalicylaldehyde, applied in chemical instruments and methods, preparation of organic compounds, organic chemistry, etc., can solve problems such as pollution and high cost, achieve simple operation and post-processing, short reaction time, overcome abnormal Construct effect

Active Publication Date: 2022-03-08
CHANGZHOU VOCATIONAL INST OF ENG
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, halogenated aromatic hydrocarbons are environmentally harmful substances, and there are also problems such as high cost or serious pollution in the later reduction reaction.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A kind of method of synthesizing mesalamine
  • A kind of method of synthesizing mesalamine
  • A kind of method of synthesizing mesalamine

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] Add p-nitrophenol (14g, 0.1mol), p-toluenesulfonic acid (26g, 0.15mol) and absolute ethanol (150ml) in sequence in a four-necked reaction flask, slowly raise the temperature to 65°C, and add hexamethylene in 3 batches Tetramine (21g, 0.15mol) was reacted at 78°C for 2h. After the reaction was completed, the heating was stopped, and ice water was poured into the reaction solution, and it was raised to room temperature under stirring. A light yellow solid was precipitated, filtered, washed, and dried to obtain Pale yellow solid 5-nitrosalicylaldehyde (15.5g, 86.5%), purity 96.91%, 1 HNMR schematic diagram as figure 1 shown.

Embodiment 2

[0040] Add p-nitrophenol (14g, 0.1mol), p-toluenesulfonic acid (34.7g, 0.2mol) and absolute ethanol (150ml) in sequence in a four-necked reaction flask, slowly raise the temperature to 78°C, and add hexaethylene in 3 batches Methyltetramine (56g, 0.4mol), reacted at 78°C for 2h. After the reaction was completed, stop heating, pour ice water into the reaction solution, and raise it to room temperature under stirring. A light yellow solid precipitated, filtered, washed, and dried. 5-nitrosalicylaldehyde (16.7 g, 89.4%) was obtained as a pale yellow solid with a purity of 95.42%.

[0041] (2) Preparation of 5-nitrosalicylic acid

Embodiment 3

[0043] Add 5-nitrosalicylaldehyde (16.7g, 0.1mol), potassium tert-butoxide (22.4g, 0.2mol), copper bromide (1.1g, 5mmol) and acetonitrile (250ml) successively in the reaction flask, stir Add 70% tert-butyl hydroperoxide (26g, 0.1mol) dropwise and react at 80°C for 5h. After the reaction is over, concentrate under reduced pressure to remove the solvent, pour cold water into the residue, stir, and filter with suction. The filtrate is washed with hydrochloric acid Adjust the pH to 2-3, filter with suction, and dry to obtain 5-nitrosalicylic acid (13.6 g, 89.34%) as a pale yellow solid with a purity of 97.31%. 1 HNMR schematic diagram as figure 2 shown.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a method for synthesizing mesalazine: 1) adding p-nitrophenol, p-toluenesulfonic acid, anhydrous ethanol and hexamethylenetetramine, stopping heating after the reaction is completed, and stirring ice water to room temperature , the solid is separated out, filtered, washed, and dried to obtain 5-nitrosalicylaldehyde; 2) add 5-nitrosalicylaldehyde, potassium tert-butoxide, copper salt and acetonitrile, add tert-butyl hydroperoxide under stirring, and react After finishing, concentrate under reduced pressure to remove solvent, pour cold water into the residue, stir, suction filter, adjust pH of filtrate with hydrochloric acid, suction filter, dry to obtain 5-nitrosalicylic acid; 3) add stannous chloride dihydrate compound, concentrated hydrochloric acid, 5-nitrosalicylic acid, ethanol, concentrated under reduced pressure after the reaction, the residue was dissolved in water, adjusted to pH with concentrated hydrochloric acid solution, left to stand for crystallization, suction filtered, the filter cake was washed with water, and dried to obtain Mesalamine. The invention has no isomers, high yield, no high temperature and high pressure conditions, low reaction cost, and no raw and auxiliary materials with high toxicity and heavy environmental pollution.

Description

technical field [0001] The invention belongs to the field of chemical reagent preparation and relates to a method for synthesizing mesalazine. Background technique [0002] Mesalamine, also known as masalazine, chemical name 5-amino-2-hydroxybenzoic acid (5-ASA), 5-aminosalicylic acid, is a drug for the treatment of ulcerative colitis. Compared with other similar drugs, mesalamine has the characteristics of colon-specific release, low toxicity, low adverse reactions and strong tolerance. [0003] The preparation method of mesalamine mainly contains four kinds at present. [0004] 1. Salicylic acid nitration reduction method. This method uses salicylic acid as raw material, synthesizes 5-nitrosalicylic acid through nitration reaction, and then reduces it to obtain 5-aminosalicylic acid. Although the process is mature, due to the positioning effect of the hydroxyl and carboxyl groups in the intermediate nitrobenzene molecule, the selectivity of the nitration reaction is poo...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C07C227/04C07C229/64
CPCC07C201/12C07C227/04C07C205/44C07C205/59C07C229/64
Inventor 张文雯巩冰倩杨利苹翁智兵叶爱英王聿鹏
Owner CHANGZHOU VOCATIONAL INST OF ENG
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products