RU2000111550A - ADDITION PRODUCTS AMIN DIEPHIR - Google Patents
ADDITION PRODUCTS AMIN DIEPHIRInfo
- Publication number
- RU2000111550A RU2000111550A RU2000111550/04A RU2000111550A RU2000111550A RU 2000111550 A RU2000111550 A RU 2000111550A RU 2000111550/04 A RU2000111550/04 A RU 2000111550/04A RU 2000111550 A RU2000111550 A RU 2000111550A RU 2000111550 A RU2000111550 A RU 2000111550A
- Authority
- RU
- Russia
- Prior art keywords
- formula
- product
- diester
- amine
- addition
- Prior art date
Links
- 150000001412 amines Chemical class 0.000 claims 7
- 150000001875 compounds Chemical class 0.000 claims 4
- 239000002253 acid Substances 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- FYSNRJHAOHDILO-UHFFFAOYSA-N Thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims 2
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 2
- 208000004434 Calcinosis Diseases 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 235000013361 beverage Nutrition 0.000 claims 1
- 238000004061 bleaching Methods 0.000 claims 1
- 125000004432 carbon atoms Chemical group C* 0.000 claims 1
- 238000004140 cleaning Methods 0.000 claims 1
- 239000008139 complexing agent Substances 0.000 claims 1
- 239000000498 cooling water Substances 0.000 claims 1
- 230000000875 corresponding Effects 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000002781 deodorant agent Substances 0.000 claims 1
- 239000003599 detergent Substances 0.000 claims 1
- -1 ester compound Chemical class 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 239000000835 fiber Substances 0.000 claims 1
- 235000013305 food Nutrition 0.000 claims 1
- 239000012458 free base Substances 0.000 claims 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000004014 plasticizer Substances 0.000 claims 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000011780 sodium chloride Substances 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 239000004753 textile Substances 0.000 claims 1
Claims (1)
где R1, R2, R3 и R4, независимо один от другого, каждый обозначает С4-С22-алкил, С2-С22-алкенил или С5-С7-циклоалкил;
X1 и Х2, независимо один от другого, каждый обозначает водород; С1-С4-алкил, С2-С4-гидроксиалкил или С2-С4-гидроксигалоалкил;
Y означает радикал формулы (1b)
A1 означает С2-С3-алкилен или 2-гидрокси-n-пропилен;
Х3 означает водород; С1-С4-алкил, С2-С4-гидроксиалкйл или С2-С4-гидроксигалоалкил;
означает асимметрический атом углерода в R- или S-конфигурации, причем, если
C1= R, C2= R;
C1= S, C2= S и
C1= R, C2= S;
m1 равняется 1 или 2 и
n означает целое число от 1 до 4;
р равняется 0 или 1;
при этом продукт присоединения может быть в виде свободного основания, кислоты, кислой соли или соли четвертичного аммония.1. The product of the addition of diester of the amine of the formula
where R 1 , R 2 , R 3 and R 4 , independently of one another, are each C 4 -C 22 alkyl, C 2 -C 22 alkenyl or C 5 -C 7 cycloalkyl;
X 1 and X 2 , independently of one another, each is hydrogen; C 1 -C 4 alkyl, C 2 -C 4 hydroxyalkyl or C 2 -C 4 hydroxyhaloalkyl;
Y is a radical of formula (1b)
A 1 is C 2 -C 3 alkylene or 2-hydroxy-n-propylene;
X 3 means hydrogen; C 1 -C 4 alkyl, C 2 -C 4 hydroxyalkyl or C 2 -C 4 hydroxyhaloalkyl;
means an asymmetric carbon atom in the R or S configuration, and if
C 1 = R, C 2 = R;
C 1 = S, C 2 = S and
C 1 = R, C 2 = S;
m 1 is 1 or 2 and
n is an integer from 1 to 4;
p is 0 or 1;
wherein the addition product may be in the form of a free base, an acid, an acid salt or a quaternary ammonium salt.
6. Использование продукта присоединения диэфир амина формулы
где R1, R2, R3, R4, X1 и X2, Y и n имеют значения, приведенные в п. 1, в качестве комплексообразователя.5. A method of obtaining a compound of formula (1), in which diaminotetracarboxylic acid of formula (lg) is reacted with thionyl chloride and an alcohol to obtain the corresponding ester compound of formula (1f) in accordance with the following scheme:
6. Use of the product of addition of the diester of the amine of the formula
where R 1 , R 2 , R 3 , R 4 , X 1 and X 2 , Y and n have the meanings given in paragraph 1, as a complexing agent.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP97810833.0 | 1997-11-06 | ||
EP97810833 | 1997-11-06 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2000111550A true RU2000111550A (en) | 2002-05-10 |
RU2189972C2 RU2189972C2 (en) | 2002-09-27 |
Family
ID=8230459
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000111550/04A RU2189972C2 (en) | 1997-11-06 | 1998-10-27 | Compounds of dietheramine addition and method of their synthesis |
Country Status (12)
Country | Link |
---|---|
US (1) | US6369268B1 (en) |
EP (1) | EP1028939A1 (en) |
JP (1) | JP2001522827A (en) |
KR (1) | KR20010031809A (en) |
CN (1) | CN1278243A (en) |
AU (1) | AU751838B2 (en) |
BR (1) | BR9813987A (en) |
IL (1) | IL135545A0 (en) |
NZ (1) | NZ504290A (en) |
PL (1) | PL340309A1 (en) |
RU (1) | RU2189972C2 (en) |
WO (1) | WO1999024392A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20060011295A1 (en) * | 2004-07-14 | 2006-01-19 | Karsten Danielmeier | Aspartic ester functional compounds |
GB0714575D0 (en) | 2007-07-26 | 2007-09-05 | Innospec Ltd | Composition |
US8163861B2 (en) * | 2009-01-15 | 2012-04-24 | Living Proof, Inc. | Beta-amino ester compounds and uses thereof |
ES2702428T3 (en) * | 2010-11-15 | 2019-02-28 | Life Technologies Corp | Transfection reagents containing amine and methods for preparing and using them |
EP2612846A1 (en) * | 2012-01-09 | 2013-07-10 | Bayer MaterialScience AG | Beta amino acid esters and use of same |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH575909A5 (en) * | 1972-08-21 | 1976-05-31 | Ciba Geigy Ag | |
DE4439421A1 (en) | 1994-11-04 | 1996-05-09 | Huels Chemische Werke Ag | New polyamines containing urea groups and processes for their preparation |
GB9507661D0 (en) * | 1995-04-13 | 1995-05-31 | Ass Octel | Process |
US5652301A (en) | 1996-08-20 | 1997-07-29 | Bayer Corporation | Aqueous polyurea dispersions and their use for preparing coatings with excellent hydrolytic and thermal stability |
-
1998
- 1998-10-27 RU RU2000111550/04A patent/RU2189972C2/en not_active IP Right Cessation
- 1998-10-27 BR BR9813987-8A patent/BR9813987A/en not_active IP Right Cessation
- 1998-10-27 US US09/530,537 patent/US6369268B1/en not_active Expired - Fee Related
- 1998-10-27 WO PCT/EP1998/006811 patent/WO1999024392A1/en not_active Application Discontinuation
- 1998-10-27 IL IL13554598A patent/IL135545A0/en unknown
- 1998-10-27 CN CN98810815A patent/CN1278243A/en active Pending
- 1998-10-27 NZ NZ504290A patent/NZ504290A/en unknown
- 1998-10-27 PL PL98340309A patent/PL340309A1/en unknown
- 1998-10-27 AU AU20478/99A patent/AU751838B2/en not_active Ceased
- 1998-10-27 JP JP2000520406A patent/JP2001522827A/en active Pending
- 1998-10-27 EP EP98965144A patent/EP1028939A1/en not_active Withdrawn
- 1998-10-27 KR KR1020007004878A patent/KR20010031809A/en not_active Application Discontinuation
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