CN106117134A - The synthetic method of medical material 5-fluoro-2-bromine isonicotinic acid - Google Patents

The synthetic method of medical material 5-fluoro-2-bromine isonicotinic acid Download PDF

Info

Publication number
CN106117134A
CN106117134A CN201510749089.6A CN201510749089A CN106117134A CN 106117134 A CN106117134 A CN 106117134A CN 201510749089 A CN201510749089 A CN 201510749089A CN 106117134 A CN106117134 A CN 106117134A
Authority
CN
China
Prior art keywords
fluoro
isonicotinic acid
synthetic method
medical material
bromine isonicotinic
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201510749089.6A
Other languages
Chinese (zh)
Inventor
彭海燕
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
WUXI QIANHAO BIO-PHARMACEUTICAL Co Ltd
Original Assignee
WUXI QIANHAO BIO-PHARMACEUTICAL Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by WUXI QIANHAO BIO-PHARMACEUTICAL Co Ltd filed Critical WUXI QIANHAO BIO-PHARMACEUTICAL Co Ltd
Priority to CN201510749089.6A priority Critical patent/CN106117134A/en
Publication of CN106117134A publication Critical patent/CN106117134A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/79Acids; Esters
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/79Acids; Esters
    • C07D213/803Processes of preparation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)

Abstract

The present invention relates to the synthetic method of a kind of medical material 5-fluoro-2-bromine isonicotinic acid, with 2,5-dibromo pyridine is raw material, utilizes displacement method to prepare 5-fluoro-2-bromopyridine under certain solvent and catalyst action, the most further by hydroxylating, generate 5-fluoro-2-bromine isonicotinic acid.The synthetic method of medical material 5-of the present invention fluoro-2-bromine isonicotinic acid is simple, efficient, and operates safety, very useful in concrete production.

Description

The synthetic method of medical material 5-fluoro-2-bromine isonicotinic acid
Technical field
The present invention relates to the synthetic method of a kind of medical material 5-fluoro-2-bromine isonicotinic acid.
Background technology
5-fluoro-2-bromine isonicotinic acid is the initiation material of many pharmaceutical synthesis, the important intermediate of particularly a lot of pyridine compounds, the most domestic synthetic method having no this compound of report.
Summary of the invention
It is an object of the invention to overcome above-mentioned deficiency, it is provided that a kind of simple, efficiently, the synthetic method of the medical material 5-fluoro-2-bromine isonicotinic acid of safety operation.
The object of the present invention is achieved like this:
The synthetic method of a kind of medical material 5-fluoro-2-bromine isonicotinic acid, with 2,5-dibromo pyridine is raw material, utilizes displacement method to prepare 5-fluoro-2-bromopyridine, the most further by hydroxylating, generate 5-fluoro-2-bromine isonicotinic acid under certain solvent and catalyst action.
Compared with prior art, the invention has the beneficial effects as follows:
The synthetic method of medical material 5-of the present invention fluoro-2-bromine isonicotinic acid is simple, efficient, and operates safety, very useful in concrete production.
Detailed description of the invention
The synthetic method of medical material 5-of the present invention fluoro-2-bromine isonicotinic acid is specific as follows:
With 2,5-dibromo pyridine is raw material, utilizes displacement method to prepare 5-fluoro-2-bromopyridine, the most further by hydroxylating, generate 5-fluoro-2-bromine isonicotinic acid under certain solvent and catalyst action.The purity of this crude product can meet general reaction requirement, can direct plunge in reaction.

Claims (1)

1. the synthetic method of a medical material 5-fluoro-2-bromine isonicotinic acid, it is characterized in that with 2,5-dibromo pyridine is raw material, utilizes displacement method to prepare 5-fluoro-2-bromopyridine under certain solvent and catalyst action, the most further by hydroxylating, generate 5-fluoro-2-bromine isonicotinic acid.
CN201510749089.6A 2015-11-08 2015-11-08 The synthetic method of medical material 5-fluoro-2-bromine isonicotinic acid Pending CN106117134A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510749089.6A CN106117134A (en) 2015-11-08 2015-11-08 The synthetic method of medical material 5-fluoro-2-bromine isonicotinic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510749089.6A CN106117134A (en) 2015-11-08 2015-11-08 The synthetic method of medical material 5-fluoro-2-bromine isonicotinic acid

Publications (1)

Publication Number Publication Date
CN106117134A true CN106117134A (en) 2016-11-16

Family

ID=57471603

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510749089.6A Pending CN106117134A (en) 2015-11-08 2015-11-08 The synthetic method of medical material 5-fluoro-2-bromine isonicotinic acid

Country Status (1)

Country Link
CN (1) CN106117134A (en)

Similar Documents

Publication Publication Date Title
CN106117134A (en) The synthetic method of medical material 5-fluoro-2-bromine isonicotinic acid
CN106117135A (en) The synthetic method of medical material 5-fluoro-2-chloroisonicotinic acid
CN106146289A (en) The synthetic method of medicine intermediate 4-oxo cyclobutane yl carboxylic acid salt
CN106117210A (en) The synthetic method of medicine intermediate hydroxyl 3-hydroxypyrrole pyrimidine
CN105777527A (en) Synthesis method of medicine intermediate 3-oxocyclobutanecarboxylic acid
CN105753771A (en) A synthetic method of a medical intermediate trans-3-N-boc-aminopiperidine
CN106146389A (en) The synthetic method of medicine intermediate 1-acetyl-4-(2-ethoxy) pyridine
CN105753780A (en) A synthetic method of a medicine raw material 5-bromo-2-chloroisonicotinic acid
CN106117122A (en) The synthetic method of medicine intermediate 1-tertbutyloxycarbonyl-2-ethoxy pyridine
CN106117103A (en) The synthetic method of medicine intermediate 1-tertbutyloxycarbonyl-3-(methoxymethyl-carbamyl) pyrrolidine
CN106117119A (en) The synthetic method of medicine intermediate 1-tertbutyloxycarbonyl-2-picoline
CN106117108A (en) The synthetic method of medicine intermediate 1-tertbutyloxycarbonyl-3-methylpyrrole piperidines
CN106117109A (en) The synthetic method of medicine intermediate 1-tertbutyloxycarbonyl-2-crassitude
CN106146390A (en) The synthetic method of medicine intermediate 2-acetyl-4-(2-methyl) pyridine
CN106117151A (en) The synthetic method of medicine intermediate 1-tertbutyloxycarbonyl-3-(methoxymethyl-carbamyl) piperazine
CN106146375A (en) The synthetic method of medicine intermediate 1-acetyl-4-(2-ethoxy) pyrrolidines
CN106146272A (en) The synthetic method of medical material 2-hydrochloric acid-3-chlorobenzene acetaldehyde
CN106146415A (en) The synthetic method of medicine intermediate 2,4-bis-chloro-5-trifluoromethyl piperazine
CN106117106A (en) The synthetic method of medicine intermediate 1-tertbutyloxycarbonyl-3-ethyl pyrrolidone
CN106117107A (en) The synthetic method of medicine intermediate 1-tertbutyloxycarbonyl-4-methyl pyrrolidone
CN106146273A (en) The synthetic method of medical material 2-ethyl-2-hydroxy-cyclohexanone
CN106146275A (en) The synthetic method of medical material 2-methyl-3-ethyl cyclohexanone
CN106117208A (en) The synthetic method of medicine intermediate 5-ethoxy pyrrolopyrimidine
CN106146377A (en) The synthetic method of medicine intermediate 4-dimethylamino pyrrolidones
CN106117158A (en) The synthetic method of medicine intermediate 2-hydroxymorpholine hydrochlorate

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20161116