SU480703A1 - The method of obtaining anthra- (1.9 sun) -pyrrole-1-carboxylic acid or its halo derivatives - Google Patents

The method of obtaining anthra- (1.9 sun) -pyrrole-1-carboxylic acid or its halo derivatives

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Publication number
SU480703A1
SU480703A1 SU1978405A SU1978405A SU480703A1 SU 480703 A1 SU480703 A1 SU 480703A1 SU 1978405 A SU1978405 A SU 1978405A SU 1978405 A SU1978405 A SU 1978405A SU 480703 A1 SU480703 A1 SU 480703A1
Authority
SU
USSR - Soviet Union
Prior art keywords
carboxylic acid
pyrrole
anthra
sun
obtaining
Prior art date
Application number
SU1978405A
Other languages
Russian (ru)
Inventor
Михаил Васильевич Казанков
Нина Петровна Макшанова
Елизавета Георгиевна Кузнецова
Original Assignee
Предприятие П/Я А-7850
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Application filed by Предприятие П/Я А-7850 filed Critical Предприятие П/Я А-7850
Priority to SU1978405A priority Critical patent/SU480703A1/en
Application granted granted Critical
Publication of SU480703A1 publication Critical patent/SU480703A1/en

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Description

ту, т. пл. 296 297°С (из водного ацетона).that, t. pl. 296 297 ° С (from aqueous acetone).

Найдено, %: С 72,99, 73,22; Н 3,75, 3,59; N 5,68, 5,57.Found,%: C 72.99, 73.22; H 3.75, 3.59; N 5.68, 5.57.

CieHgNOs.CieHgNOs.

Вычислено, %: С 73,00; Н 3,43; N 5,32.Calculated,%: C 73.00; H 3.43; N 5.32.

Аналогично, использу  вместо ацетата натри  бикарбонат натри , получают антра 1 ,9Ьс -пиррол-1-карбоновую кислоту.Similarly, using sodium bicarbonate instead of sodium acetate, antra 1, 9Bc -pyrrole-1-carboxylic acid is obtained.

Пример 2. 1 г сульфата 6-бром-4-метилантраоиридонил-Ьдиазони , нолученного из 1-амино-6-бром-4-метилантраниридона в услови х примера 1, в«ос т в 100 мл 2%-иого раствора ацетата натри , неремешивают несколько МИнут и отфильтровывают 0,7 г (90%) 5-бром- 3 -метиллирролантрон- 1 -карбоновой кислоты, т. ил. выше 350°С (из водного дноксана ).Example 2: 1 g of 6-bromo-4-methylanthraoiridonyl-Lyzonium sulphate, obtained from 1-amino-6-bromo-4-methylanthraniridone under the conditions of example 1, was dissolved in 100 ml of 2% sodium acetate solution, do not mix up a few minutes and filter 0.7 g (90%) of 5-bromo-3-methyrrolantan-1-carboxylic acid, t. Il. above 350 ° C (from water lenoxan).

Найдено, %: С 57,31, 57,60; Н 2,68, 2,57; N 4,06, 3,80.Found,%: C 57.31, 57.60; H 2.68, 2.57; N 4.06, 3.80.

СпНюМОзВг.SPNMOZVg.

Вычислено, %: С 57,32; Н 2,54; N 3,93.Calculated,%: C 57.32; H 2.54; N 3.93.

Аналогично из 1-амшю-6-хлорантрапиридона получают 5-хлорпирролантрои-1-карбонов у ю кислоту.Similarly, from 1-H-6-chloro-anthrapyridone, 5-chloropyrrolanthro-1-carboxylic acid is obtained.

Предмет изобретени Subject invention

Способ полу1чени  антра- 1,9Ьс -пиррол-1карбоиовой кислоты или ее галоидпроизводиых , отличающийс  тем, что 1-аминоантрапиридОН или его галоидзамещенные подвергают диазотированию и полученные соли антрапиридонил-1-диазони  обрабатывают щелочными агентами, наприатер ацетатом натри , с последующим выделением целевого продукта известными приемами.Method polu1cheni anthracene 1,9s -pyrrole-1karboiovoy acid or galoidproizvodiyh, characterized in that 1-aminoantrapiridON or halogenated subjected to diazotization and the resulting salt anthrapyridone-1-diazonium treated with alkaline agents, napriater sodium acetate, followed by isolation of the desired product by known tricks.

SU1978405A 1973-12-24 1973-12-24 The method of obtaining anthra- (1.9 sun) -pyrrole-1-carboxylic acid or its halo derivatives SU480703A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SU1978405A SU480703A1 (en) 1973-12-24 1973-12-24 The method of obtaining anthra- (1.9 sun) -pyrrole-1-carboxylic acid or its halo derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SU1978405A SU480703A1 (en) 1973-12-24 1973-12-24 The method of obtaining anthra- (1.9 sun) -pyrrole-1-carboxylic acid or its halo derivatives

Publications (1)

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SU480703A1 true SU480703A1 (en) 1975-08-15

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