TOP > 外国特許検索 > Reagent for determining the absolute configuration of chiral compound and determination method

Reagent for determining the absolute configuration of chiral compound and determination method

外国特許コード F110005279
整理番号 E04706US
掲載日 2011年8月29日
出願国 アメリカ合衆国
出願番号 50590603
公報番号 20050107604
公報番号 7648841
出願日 平成15年1月10日(2003.1.10)
公報発行日 平成17年5月19日(2005.5.19)
公報発行日 平成22年1月19日(2010.1.19)
国際出願番号 JP2003000147
国際公開番号 WO2003073076
国際出願日 平成15年1月10日(2003.1.10)
国際公開日 平成15年9月4日(2003.9.4)
優先権データ
  • 特願2002-051505 (2002.2.27) JP
  • 2003WO-JP00147 (2003.1.10) WO
発明の名称 (英語) Reagent for determining the absolute configuration of chiral compound and determination method
発明の概要(英語) (US7648841)
The present invention relates to a reagent for determining the absolute configuration of a chiral compound containing as an active ingredient a metalloporphyrin dimer, wherein the metalloporphyrin dimer has an alkaline-earth metal ion as a central metal and has a carbon chain-crosslinked structure in which at least one of the two porphyrin rings has a substituent bulkier than methyl at least one of the second carbon atoms from a carbon atom bonded to the crosslinking carbon chain along the outer periphery of the porphyrin ring and a method for determining the absolute configuration of an asymmetric carbon atom of the chiral compound using the reagent.
特許請求の範囲(英語) [claim1]
1. A reagent for determining the absolute configuration of a chiral compound, the reagent containing as an active ingredient a metalloporphyrin dimer comprising two porphyrin rings, wherein the metalloporphyrin dimer has Mg2+ as a central metal and has a carbon chain-crosslinked structure in which at least one of the two porphyrin rings has a substituent bulkier than methyl at at least one carbon atom located two carbon atoms away from a carbon atom bonded to the crosslinking carbon chain along the outer periphery of the porphyrin ring, and wherein an induced Cotton effect can be detected by said metalloporphyrin dimer in the case of a chiral compound of a monoalcohol without cooling to about -80 deg. C.
[claim2]
2. A reagent for determining the absolute configuration of a chiral compound according to claim 1, wherein the carbon chain-crosslinked metalloporphyrin dimer is a metalloporphyrin represented by formula (1):
wherein M2+ and M'2+ are Mg2+,
n is 2 or 3,
Ra to Rd are the same or different and each represent a hydrogen atom or a substituent bulkier than methyl,
at least one of Ra to Rd represents a substituent bulkier than methyl, and
R1 to R12 are the same or different and each represent a hydrogen atom or a hydrocarbon group.
[claim3]
3. A reagent according to claim 2, wherein at least one of Ra to Rd in formula (1) is one member selected from the group consisting of 1) a C1-C8 hydrocarbon group, 2) an oxygen-containing substituent, 3) a nitrogen-containing substituent, 4) a halogen atom, and 5) a halogenated hydrocarbon group.
[claim4]
4. A method for determining the absolute configuration of a chiral compound comprising analyzing a sample solution containing a reagent according to claim 1 and the chiral compound by circular dichroism spectrophotometry to determine the absolute configuration of an asymmetric carbon of the chiral compound based on a sign of the Cotton effect, the chiral compound having the following characteristics: (i) being capable of coordinating to the metalloporphyrin dimer as an active ingredient, and
(ii) having a group capable of coordinating to the metalloporphyrin dimer directly bonded to the asymmetric carbon atom, or having one carbon atom separating the group capable of coordinating to the metalloporphyrin dimer and the asymmetric carbon atom, wherein an induced Cotton effect can be detected by said metalloporphyrin dimer in the case of a chiral compound of a monoalcohol without cooling to about -80 deg. C.
[claim5]
5. A method according to claim 4, wherein the chiral compound is selected from one member of the group consisting of 1) a primary monoamine, 2) a secondary monoamine, 3) a monoalcohol, and 4) an aminoalcohol.
[claim6]
6. A method according to claim 4, wherein the circular dichroism spectrophotometric measurement is conducted at -10 deg. C. to 30 deg. C.
[claim7]
7. A method for determining an absolute configuration of a chiral compound, comprising: providing a chiral compound (i) being capable of coordinating to the metalloporphyrin dimer according to claim 1 as an active ingredient and (ii) having a group capable of coordinating to the metalloporphyrin dimer directly bonded to an asymmetric carbon atom, or having one carbon atom separating the group capable of coordinating to the metalloporphyrin dimer and the asymmetric carbon atom;
providing a sample solution containing the chiral compound and a reagent, said reagent containing as an active ingredient a metalloporphyrin dimer, wherein the metalloporphyrin dimer has two porphyrin rings and a crosslinking carbon chain which bonds the two porphyrin rings, each porphyrin ring has Mg2+ as a central metal, and at least one of the two porphyrin rings has a substituent bulkier than methyl at at least one of carbon atoms which are positioned secondarily along the outer periphery of the porphyrin ring based on a carbon atom bonded to the crosslinking carbon chain; and
subjecting the sample solution to circular dichroism spectrophotometry to determine the absolute configuration of an asymmetric carbon of the chiral compound based on a sign of the Cotton effect, wherein an induced Cotton effect can be detected by said metalloporphyrin dimer in the case of a chiral compound of a monoalcohol without cooling to about -80 deg. C.
[claim8]
8. The method according to claim 7, wherein the chiral compound is selected from one member of the group consisting of 1) a primary monoamine, 2) a secondary monoamine, 3) a monoalcohol, and 4) an aminoalcohol.
[claim9]
9. The method according to claim 7, wherein the carbon chain-crosslinked metalloporphyrin dimer is a metalloporphyrin represented by formula (1):
wherein M2+ and M'2+ are Mg2+; n is 2 or 3; Ra to Rd are the same or different and each represent a hydrogen atom or a substituent bulkier than methyl; at least one of Ra to Rd represents a substituent bulkier than methyl; and R1 to R12 are the same or different and each represent a hydrogen atom or a hydrocarbon group.
[claim10]
10. The method according to claim 7, wherein the circular dichroism spectrophotometric measurement is conducted at -10 deg. C. to 30 deg. C.
[claim11]
11. A reagent for determining an absolute configuration of a chiral compound, the reagent containing as an active ingredient a metalloporphyrin dimer, wherein the metalloporphyrin dimer has two porphyrin rings and a crosslinking carbon chain which bonds the two porphyrin rings, each porphyrin ring has Mg2+ as a central metal, and at least one of the two porphyrin rings has a substituent bulkier than methyl at at least one of carbon atoms which are positioned secondarily along the outer periphery of the porphyrin ring based on a carbon atom bonded to the crosslinking carbon chain, wherein an induced Cotton effect can be detected by said metalloporphyrin dimer in the case of a chiral compound of a monoalcohol without cooling to about -80 deg. C.
[claim12]
12. A mixture of a chiral compound and a reagent for determining an absolute configuration of the chiral compound, said reagent containing as an active ingredient a metalloporphyrin dimer having two porphyrin rings and a crosslinking carbon chain which bonds the two porphyrin rings, each porphyrin ring has Mg2+ as a central metal, and at least one of the two porphyrin rings has a substituent bulkier than methyl at at least one of carbon atoms which are positioned secondarily along the outer periphery of the porphyrin ring based on a carbon atom bonded to the crosslinking carbon chain, wherein an induced Cotton effect can be detected by said metalloporphyrin dimer in the case of a chiral compound of a monoalcohol without cooling to about -80 deg. C.
[claim13]
13. The mixture according to claim 12, wherein the carbon chain-crosslinked metalloporphyrin dimer is a metalloporphyrin represented by formula (1):
wherein M2+ and M'2+ are Mg2+; n is 2 or 3; Ra to Rd are the same or different and each represent a hydrogen atom or a substituent bulkier than methyl; at least one of Ra to Rd represents a substituent bulkier than methyl; and R1 to R12 are the same or different and each represent a hydrogen atom or a hydrocarbon group.
[claim14]
14. The mixture according to claim 12, wherein the chiral compound (i) is capable of coordinating to the metalloporphyrin dimer as an active ingredient and (ii) has a group capable of coordinating to the metalloporphyrin dimer directly bonded to an asymmetric carbon atom, or has one carbon atom separating the group capable of coordinating to the metalloporphyrin dimer and the asymmetric carbon atom.
[claim15]
15. The mixture according to claim 14, wherein the chiral compound is selected from one member of the group consisting of 1) a primary monoamine, 2) a secondary monoamine, 3) a monoalcohol, and 4) an aminoalcohol.
[claim16]
16. The mixture according to claim 12, which is a solution.
  • 発明者/出願人(英語)
  • INOUE YOSHIHISA
  • BOROVKOV VICTOR
  • LINTULUOTO JUHA
  • JAPAN SCIENCE AND TECHNOLOGY AGENCY
国際特許分類(IPC)
米国特許分類/主・副
  • 436/96
  • 252/408.1
  • 436/73
  • 436/79
  • 436/91
  • 436/106
  • 436/164
  • 436/166
  • 436/171
  • 540/145
  • 562/401
参考情報 (研究プロジェクト等) ERATO INOUE Photo-chirogenesis AREA
ライセンスをご希望の方、特許の内容に興味を持たれた方は、問合せボタンを押してください。

PAGE TOP

close
close
close
close
close
close