A kind of synthetic method of acrylic acid derivative
A synthesis method and a derivative technology, applied in the direction of organic chemistry, etc., can solve the problem of no literature report in the synthesis, and achieve the effect of simple reaction operation and high yield.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Publication Date
- 2020-09-01
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Abstract
Description
technical field
[0001] The invention belongs to the field of organic synthesis, and in particular relates to a method for synthesizing acrylic acid derivatives. Background technique
[0002] Histidine is one of the essential amino acids for humans. Its main function is to maintain the healthy development of various tissues in the body, especially the myelin sheath that wraps nerve cells, and ensures the transmission of information from the brain to various parts of the body. It has a certain effect on the treatment of mental illness, rheumatoid arthritis, deafness caused by nerve damage, nephrogenic anemia and uremia. In addition, polypeptides containing histidine structural units also have various biological activities. In 2000, Mao Yumin and others discovered that a polypeptide containing a histidine fragment had therapeutic effects on arrhythmia, bronchial asthma, acute pancreatitis, diabetes, and albinism (CN1342770A). In 2016, Wu Junchen and others from East China Uni...
Examples
Embodiment 1
[0022] Example 1: Methyl 2-((S)-2-(tert-butoxycarbonylamino)-3-(1-trityl-1H-imidazole-4-yl)propionamide)-3-hydroxypropionate preparation of
[0023]
[0024] Dissolve (S)-2-(tert-butoxycarbonylamino)-3-(1-trityl-1H-imidazole-4-yl)propionic acid 2200g (4.42mol, 1.0eq) in dimethylformamide In 15L, add pyridine 1042g (13.17mol, 3.0eq), add serine methyl ester hydrochloride 753g (4.84mol, 1.1eq); add EDCI 1011g (5.30mol, 1.2eq) in batches, control the internal temperature to less than 15°C, After addition, react at 20-30°C for 3h. The reaction solution was poured into 45 L of ice water, and a large amount of solids precipitated out. Filter, dissolve the filter cake with 15L of EA / THF=5 / 1, wash once with 5L of 1N HCl, wash once with 5L of saturated saline, and dry sodium sulfate. Filter, concentrate the organic phase under reduced pressure until a large amount of solids precipitate, add 5L of petroleum ether to make a slurry, filter, and dry to obtain 2-((S)-2-(tert-butoxycar...
Embodiment 2
[0025] Example 2: 2-((S)-2-(tert-butoxycarbonylamino)-3-(1-trityl-1H-imidazole-4-yl)propionamide)-3-methanesulfonyloxy Preparation of methyl propionate:
[0026]
Embodiment 3
[0028] Example 3: Preparation of (S)-2-(2-(tert-butoxycarbonylamino)-3-(1-trityl-1H-imidazole-4-yl)propionamide)methyl acrylate:
[0029]