RU2008136831A - SUBSTITUTED 2H, 8H-1,4-DIOXA-9b-AZAPHENALEN-2,8-DIONES AND METHOD FOR PRODUCING THEM - Google Patents

SUBSTITUTED 2H, 8H-1,4-DIOXA-9b-AZAPHENALEN-2,8-DIONES AND METHOD FOR PRODUCING THEM Download PDF

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RU2008136831A
RU2008136831A RU2008136831/04A RU2008136831A RU2008136831A RU 2008136831 A RU2008136831 A RU 2008136831A RU 2008136831/04 A RU2008136831/04 A RU 2008136831/04A RU 2008136831 A RU2008136831 A RU 2008136831A RU 2008136831 A RU2008136831 A RU 2008136831A
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dioxa
azaphenalen
dione
trimethyl
phenyl
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RU2393162C2 (en
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Ольга Андреевна Петина (RU)
Ольга Андреевна Петина
Игорь Павлович Яковлев (RU)
Игорь Павлович Яковлев
Александр Васильевич Препьялов (RU)
Александр Васильевич Препьялов
Борис Юрьевич Лалаев (RU)
Борис Юрьевич Лалаев
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Государственное образовательное учреждение высшего профессионального образования САНКТ-ПЕТЕРБУРГСКАЯ ГОСУДАРСТВЕННАЯ ХИМИКО-ФАРМАЦ
Государственное образовательное учреждение высшего профессионального образования САНКТ-ПЕТЕРБУРГСКАЯ ГОСУДАРСТВЕННАЯ ХИМИКО-ФАРМАЦЕВТИЧЕСКАЯ АКАДЕМИЯ (ГОУ ВПО СПХФА Росздрава)
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    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

1. Замещенные 2H,8H-1,4-диокса-9b-азафенален-2,8-дионы общей формулы I ! ! где R=H, R1=Me (Ia - 3,7,9-триметил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион); ! R=H, R1=Bu (Iб - 3,7,9-трибутил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион); ! R=H, R1=cHex (Iв - 3,7,9-трициклогексил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион); ! R=Cl, R1=Me (Iг - 3,7,9-триметил-5-(n-хлорфенил)-2H,8H-1,4-диокса-9b-азафенален-2,8-дион); ! R=Br, R1=Me (Iд - 3,7,9-триметил-5-(n-бромфенил)-2H,8H-1,4-диокса-9b-азафенален-2,8-дион). ! 2. Способ получения замещенных 2H,8H-1,4-диокса-9b-азафенален-2,8-дионов общей формулы I ! ! где R=H, R1-Me (Ia - 3,7,9-триметил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион); ! R=H, R1=Bu (Iб - 3,7,9-трибутил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион); ! R=H, R1=cHex (Iв - 3,7,9-трициклогексил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион); ! R=C1, R1=Me (Iг - 3,7,9-триметил-5-(n-хлорфенил)-2H,8H-1,4-диокса-9b-азафенален-2,8-дион); ! R=Br, R1=Me (Iд - 3,7,9-триметил-5-(n-бромфенил)-2H,8H-1,4-диокса-9b-азафенален-2,8-дион), ! заключающийся в том, что амид арилпропиоловой кислоты подвергают взаимодействию с моноалкил замещенным малонилдихлоридом, взятыми в соотношении 1:3, при кипячении в среде безводного неполярного органического растворителя с последующим выделением целевого продукта.1. Substituted 2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dyons of the general formula I! ! where R = H, R1 = Me (Ia - 3,7,9-trimethyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); ! R = H, R1 = Bu (IB - 3,7,9-tributyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); ! R = H, R1 = cHex (Ib - 3,7,9-tricyclohexyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); ! R = Cl, R1 = Me (Ig - 3,7,9-trimethyl-5- (n-chlorophenyl) -2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); ! R = Br, R1 = Me (Id - 3,7,9-trimethyl-5- (n-bromophenyl) -2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione). ! 2. A method of producing substituted 2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-diones of the general formula I! ! where R = H, R1-Me (Ia - 3,7,9-trimethyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); ! R = H, R1 = Bu (IB - 3,7,9-tributyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); ! R = H, R1 = cHex (Ib - 3,7,9-tricyclohexyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); ! R = C1, R1 = Me (Ig - 3,7,9-trimethyl-5- (n-chlorophenyl) -2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); ! R = Br, R1 = Me (Id - 3,7,9-trimethyl-5- (n-bromophenyl) -2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione),! consisting in the fact that the amide of arylpropiolic acid is reacted with monoalkyl substituted malonyl dichloride taken in the ratio of 1: 3, while boiling in the medium of an anhydrous non-polar organic solvent, followed by isolation of the target product.

Claims (2)

1. Замещенные 2H,8H-1,4-диокса-9b-азафенален-2,8-дионы общей формулы I1. Substituted 2H, 8H-1,4-dioxa-9b-azaphenalene-2,8-dyons of the general formula I
Figure 00000001
Figure 00000001
 где R=H, R1=Me (Ia - 3,7,9-триметил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион);where R = H, R 1 = Me (Ia - 3,7,9-trimethyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); R=H, R1=Bu (Iб - 3,7,9-трибутил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион);R = H, R 1 = Bu (IB - 3,7,9-tributyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); R=H, R1=cHex (Iв - 3,7,9-трициклогексил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион);R = H, R 1 = cHex (Ib - 3,7,9-tricyclohexyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); R=Cl, R1=Me (Iг - 3,7,9-триметил-5-(n-хлорфенил)-2H,8H-1,4-диокса-9b-азафенален-2,8-дион);R = Cl, R 1 = Me (Ig - 3,7,9-trimethyl-5- (n-chlorophenyl) -2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); R=Br, R1=Me (Iд - 3,7,9-триметил-5-(n-бромфенил)-2H,8H-1,4-диокса-9b-азафенален-2,8-дион).R = Br, R 1 = Me (Id - 3,7,9-trimethyl-5- (n-bromophenyl) -2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione). 2. Способ получения замещенных 2H,8H-1,4-диокса-9b-азафенален-2,8-дионов общей формулы I2. The method of obtaining substituted 2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-diones of the General formula I
Figure 00000002
Figure 00000002
 где R=H, R1-Me (Ia - 3,7,9-триметил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион);where R = H, R 1 -Me (Ia - 3,7,9-trimethyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalene-2,8-dione); R=H, R1=Bu (Iб - 3,7,9-трибутил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион);R = H, R 1 = Bu (IB - 3,7,9-tributyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); R=H, R1=cHex (Iв - 3,7,9-трициклогексил-5-фенил-2H,8H-1,4-диокса-9b-азафенален-2,8-дион);R = H, R 1 = cHex (Ib - 3,7,9-tricyclohexyl-5-phenyl-2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); R=C1, R1=Me (Iг - 3,7,9-триметил-5-(n-хлорфенил)-2H,8H-1,4-диокса-9b-азафенален-2,8-дион);R = C1, R 1 = Me (Ig - 3,7,9-trimethyl-5- (n-chlorophenyl) -2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione); R=Br, R1=Me (Iд - 3,7,9-триметил-5-(n-бромфенил)-2H,8H-1,4-диокса-9b-азафенален-2,8-дион),R = Br, R 1 = Me (Id - 3,7,9-trimethyl-5- (n-bromophenyl) -2H, 8H-1,4-dioxa-9b-azaphenalen-2,8-dione), заключающийся в том, что амид арилпропиоловой кислоты подвергают взаимодействию с моноалкил замещенным малонилдихлоридом, взятыми в соотношении 1:3, при кипячении в среде безводного неполярного органического растворителя с последующим выделением целевого продукта. consisting in the fact that the amide of arylpropiolic acid is reacted with monoalkyl substituted malonyl dichloride taken in the ratio of 1: 3, while boiling in the medium of an anhydrous non-polar organic solvent, followed by isolation of the target product.
RU2008136831/04A 2008-09-12 2008-09-12 SUBSTITUTED 2H,8H-1,4-DIOXA-9b-AZAPHENALENE-2,8-DIONES AND SYNTHESIS METHOD THEREOF RU2393162C2 (en)

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