Intermediate for preparing halichondrin compound and preparation method thereof

A compound, halogen technology, used in the preparation of halichondrin or its analogs, the field of intermediate compounds of Eribulin, can solve the problem of lengthy synthetic route, cost control environment and labor protection, difficult to control the optical purity of starting materials, etc. question

Active Publication Date: 2020-06-16
BEIJING TIENYI LUFU PHARMATECH CO LTD
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] However, in the prior art, there are many defects in the preparation method of the above-mentioned compound of formula 4 or formula 6, for example, the synthetic route is too lengthy, the optical purity of the starting material is difficul

Method used

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  • Intermediate for preparing halichondrin compound and preparation method thereof
  • Intermediate for preparing halichondrin compound and preparation method thereof
  • Intermediate for preparing halichondrin compound and preparation method thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0132] Embodiment 1: Preparation method one of compound 8 (see attached figure 1 )

[0133] 1.1 Preparation of Compound 1

[0134] method one:

[0135]Add (s)-4-phenyl-2-oxazolidinone (15.6g) into a 500ml three-necked flask, add dry THF (200ml) to dissolve, change the argon and protect it with argon, then cool the reaction solution to - 78°C, add n-BuLi solution in THF (2.5M, 38ml) dropwise (keep the internal temperature ≤ -60°C), after dropping, keep the reaction at -78°C for 15min, then add crotonyl chloride (10g) dropwise, dropwise , kept at -78°C for 30min, then rose to 0°C for 1.5h. After the completion of the reaction as detected by TLC, slowly add saturated ammonium chloride solution to quench, and stir well until the solid disappears, and the layers can be clearly separated. The liquids were separated, the aqueous phase was extracted twice with ethyl acetate, and the organic phases were combined and washed once with saturated sodium chloride solution. The organic...

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Abstract

The invention relates to an intermediate for preparing a halichondrin compound and a preparation method thereof. The invention particularly relates to an intermediate for preparing halichondrin, eribulin or analogues thereof, and a preparation method and application of the intermediate. The intermediate as well as the preparation method and application thereof are used for constructing C20-C26 structural fragments of the halichondrin compound. The initial raw materials of the synthesis route are cheap, easy to obtain, stable in source and reliable in quality; the structural characteristics ofreactants are fully utilized in the selection of a chiral center construction method, so that the synthesis efficiency is practically improved, and the difficulty and risk of product quality control are reduced; and the use of a high-toxicity and expensive organic tin catalyst is avoided, so that the cost and the environmental friendliness are remarkably improved.

Description

technical field [0001] The present invention relates to intermediate compounds that can be used to prepare halichondrin or its analogs, especially eribulin, and the preparation methods of these intermediate compounds, belonging to the technical field of organic synthesis. Background technique [0002] Halichondrin (HB for short) is a kind of natural product that exists in the cavernous body and has a polyether macrolide structure. This kind of substance has a strong anti-tumor effect and broad medicinal prospects. Based on their structural differences, these natural products are divided into the following categories: norhalichondrin, halichondrin, homohalichondrin, etc., and each category has a series of representative subgroups. type, the subtype and specific structure are known in the art, and are disclosed in detail in WO2016003975A1, which is incorporated in this prior art document in its entirety; Eribulin (Eribulin, hereinafter referred to as EB) is a kind of halichond...

Claims

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Application Information

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IPC IPC(8): C07F7/18
CPCC07F7/1892C07F7/1804C07F7/0812C07D263/26C07D277/16C07D493/22
Inventor 徐为平
Owner BEIJING TIENYI LUFU PHARMATECH CO LTD
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