BE886126A - Nouveaux derives stilbeniques utilisables comme azurants optiques et leur preparation - Google Patents

Nouveaux derives stilbeniques utilisables comme azurants optiques et leur preparation Download PDF

Info

Publication number: BE886126A
Authority: BE; Belgium
Prior art keywords: emi; formula; group; carbon atoms; derivatives
Prior art date: 1979-11-14

Application number

BE1/10028A

Other languages

English (en)

French (fr)

Original Assignee

Sandoz Sa

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.)

1979-11-14

Filing date

1980-11-13

Publication date

1981-05-13

1980-11-13 Application filed by Sandoz Sa filed Critical Sandoz Sa

1981-05-13 Publication of BE886126A publication Critical patent/BE886126A/fr

Links

230000003287 optical effect Effects 0.000 title claims description 14
238000002360 preparation method Methods 0.000 title claims description 7
150000001875 compounds Chemical class 0.000 claims description 42
125000000217 alkyl group Chemical group 0.000 claims description 26
125000004432 carbon atom Chemical group C* 0.000 claims description 26
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 22
229910052801 chlorine Inorganic materials 0.000 claims description 17
238000000034 method Methods 0.000 claims description 16
150000001768 cations Chemical class 0.000 claims description 13
125000003545 alkoxy group Chemical group 0.000 claims description 12
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
229910052757 nitrogen Inorganic materials 0.000 claims description 11
239000000460 chlorine Substances 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 10
125000004433 nitrogen atom Chemical group N* 0.000 claims description 10
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 9
239000000758 substrate Substances 0.000 claims description 8
125000001309 chloro group Chemical group Cl* 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
125000001424 substituent group Chemical group 0.000 claims description 6
125000003118 aryl group Chemical group 0.000 claims description 5
125000004429 atom Chemical group 0.000 claims description 5
125000004093 cyano group Chemical group *C#N 0.000 claims description 5
239000003599 detergent Substances 0.000 claims description 5
229910052760 oxygen Inorganic materials 0.000 claims description 5
239000001301 oxygen Substances 0.000 claims description 5
239000004753 textile Substances 0.000 claims description 5
238000005282 brightening Methods 0.000 claims description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
239000004952 Polyamide Substances 0.000 claims description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
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MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
125000000129 anionic group Chemical group 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
239000000126 substance Substances 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
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LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 claims 5
125000001624 naphthyl group Chemical group 0.000 claims 1
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239000002253 acid Substances 0.000 description 6
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238000007363 ring formation reaction Methods 0.000 description 4
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239000005708 Sodium hypochlorite Substances 0.000 description 3
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IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
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239000007864 aqueous solution Substances 0.000 description 2
RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 description 2
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125000004430 oxygen atom Chemical group O* 0.000 description 1
229920002866 paraformaldehyde Polymers 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
239000012071 phase Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
239000005077 polysulfide Substances 0.000 description 1
229920001021 polysulfide Polymers 0.000 description 1
150000008117 polysulfides Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
FKRCODPIKNYEAC-UHFFFAOYSA-N propionic acid ethyl ester Natural products CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 1
WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
230000035943 smell Effects 0.000 description 1
125000004436 sodium atom Chemical group 0.000 description 1
UKLNMMHNWFDKNT-UHFFFAOYSA-M sodium chlorite Chemical compound [Na+].[O-]Cl=O UKLNMMHNWFDKNT-UHFFFAOYSA-M 0.000 description 1
229960002218 sodium chlorite Drugs 0.000 description 1
HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
229940001584 sodium metabisulfite Drugs 0.000 description 1
235000010262 sodium metabisulphite Nutrition 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
229960001922 sodium perborate Drugs 0.000 description 1
CRWJEUDFKNYSBX-UHFFFAOYSA-N sodium;hypobromite Chemical compound [Na+].Br[O-] CRWJEUDFKNYSBX-UHFFFAOYSA-N 0.000 description 1
YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000013042 solid detergent Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000005303 weighing Methods 0.000 description 1
230000037303 wrinkles Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
- C07D249/06—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D307/80—Radicals substituted by oxygen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Detergent Compositions (AREA)

BE1/10028A 1979-11-14 1980-11-13 Nouveaux derives stilbeniques utilisables comme azurants optiques et leur preparation BE886126A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB7939349		1979-11-14

Publications (1)

Publication Number	Publication Date
BE886126A true BE886126A (fr)	1981-05-13

Family

ID=10509175

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE1/10028A BE886126A (fr)	1979-11-14	1980-11-13	Nouveaux derives stilbeniques utilisables comme azurants optiques et leur preparation

Country Status (2)

Country	Link
JP (1)	JPS56106960A (ja)
BE (1)	BE886126A (ja)

1980
- 1980-11-13 BE BE1/10028A patent/BE886126A/fr not_active IP Right Cessation
- 1980-11-14 JP JP15971180A patent/JPS56106960A/ja active Pending

Also Published As

Publication number	Publication date
JPS56106960A (en)	1981-08-25

Legal Events

Date

Code

Title

Description

1985-05-31

RE

Patent lapsed

Owner name: SANDOZ S.A.

Effective date: 19841113

Publication	Publication Date	Title
BE1004045A3 (fr)	1992-09-15	Sels de colorants pour la teinture dans la masse des polyamides synthetiques.
FR2655051A1 (ja)	1991-05-31
US2901476A (en)	1959-08-25	Stilbene triazoles
FR2789387A1 (fr)	2000-08-11	Nouveau procede de preparation d'intermediaires pesticides
BE886126A (fr)	1981-05-13	Nouveaux derives stilbeniques utilisables comme azurants optiques et leur preparation
FR2468585A1 (fr)	1981-05-08	Procede de preparation de la 1,4-diamino-2,3-dicyanoanthraquinone
LU82290A1 (fr)	1980-07-01	Procede de preparation de sulfoxydes de penicilline
US4316815A (en)	1982-02-23	Bis-triazolyl and bis-pyrazolyl stilbene compounds
FR2491486A1 (fr)	1982-04-09	Nouveaux composes halogeno-triaziniques, leur preparation et leur utilisation comme colorants
FR2524468A1 (fr)	1983-10-07	Nouveaux derives condenses du thiophene, leur preparation et leur utilisation comme azurants optiques
US4144243A (en)	1979-03-13	3-Pyrozolyl-4-triazolyl compounds
BE837655A (fr)	1976-07-16	Procede de preparation de colorants cationiques purs
GB2063876A (en)	1981-06-10	Stilbene derivatives and their use as brightening agents
FR2606406A1 (fr)	1988-05-13	Derives de naphtolactames, procede pour leur preparation, et leur utilisation en tant que colorants
JP2961875B2 (ja)	1999-10-12	ベンゾジフラノン化合物の製造方法
BE531250A (ja)
US4229579A (en)	1980-10-21	3-(Halopyrazolyl)-7-triazolyl-coumarin compounds
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JPH0848893A (ja)	1996-02-20	新規ベンゾジフラノン化合物およびそれを用いる疎水性繊維材料の染色または捺染方法
BE647036A (ja)	1964-10-26