ES268522A1 - Un procedimiento para la producción de nuevos ácidos antranílicos - Google Patents

Un procedimiento para la producción de nuevos ácidos antranílicos

Info

Publication number: ES268522A1
Authority: ES; Spain
Prior art keywords: general formula; group; methyl; radical; cooh
Prior art date: 1961-01-12
Legal status (The legal status 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 status listed.): Expired

Application number

ES268522A

Other languages

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Parke Davis and Co LLC

Original Assignee

Parke Davis and Co LLC

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.)

1961-01-12

Filing date

1961-06-22

Publication date

1962-04-16

1961-06-22 Application filed by Parke Davis and Co LLC filed Critical Parke Davis and Co LLC

1962-04-16 Publication of ES268522A1 publication Critical patent/ES268522A1/es

Status Expired legal-status Critical Current

Links

239000002253 acid Substances 0.000 title abstract 2
150000007513 acids Chemical class 0.000 title 1
238000004519 manufacturing process Methods 0.000 title 1
238000000034 method Methods 0.000 title 1
150000001875 compounds Chemical class 0.000 abstract 6
-1 acyl radical Chemical class 0.000 abstract 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 4
229910052801 chlorine Inorganic materials 0.000 abstract 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
229910052783 alkali metal Inorganic materials 0.000 abstract 2
229910052784 alkaline earth metal Inorganic materials 0.000 abstract 2
239000000460 chlorine Substances 0.000 abstract 2
125000001309 chloro group Chemical group Cl* 0.000 abstract 2
150000002463 imidates Chemical class 0.000 abstract 2
230000008707 rearrangement Effects 0.000 abstract 2
150000003839 salts Chemical class 0.000 abstract 2
125000001424 substituent group Chemical group 0.000 abstract 2
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
MBISZJKAVPBLDT-UHFFFAOYSA-N 2,6-dichloro-3-ethylaniline Chemical compound CCC1=CC=C(Cl)C(N)=C1Cl MBISZJKAVPBLDT-UHFFFAOYSA-N 0.000 abstract 1
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 abstract 1
ZAQGLDMWELFZPL-UHFFFAOYSA-N 3,6-dichloro-2-methylaniline Chemical compound CC1=C(Cl)C=CC(Cl)=C1N ZAQGLDMWELFZPL-UHFFFAOYSA-N 0.000 abstract 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
208000025747 Rheumatic disease Diseases 0.000 abstract 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
238000005903 acid hydrolysis reaction Methods 0.000 abstract 1
125000002252 acyl group Chemical group 0.000 abstract 1
239000003513 alkali Substances 0.000 abstract 1
150000001340 alkali metals Chemical class 0.000 abstract 1
150000001342 alkaline earth metals Chemical class 0.000 abstract 1
125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
125000000217 alkyl group Chemical group 0.000 abstract 1
150000003931 anilides Chemical class 0.000 abstract 1
230000003110 anti-inflammatory effect Effects 0.000 abstract 1
125000005161 aryl oxy carbonyl group Chemical group 0.000 abstract 1
IAHMNSCQDXESII-UHFFFAOYSA-N benzenecarboximidoyl chloride Chemical compound ClC(=N)C1=CC=CC=C1 IAHMNSCQDXESII-UHFFFAOYSA-N 0.000 abstract 1
150000001558 benzoic acid derivatives Chemical class 0.000 abstract 1
239000002775 capsule Substances 0.000 abstract 1
230000003197 catalytic effect Effects 0.000 abstract 1
239000003795 chemical substances by application Substances 0.000 abstract 1
238000005660 chlorination reaction Methods 0.000 abstract 1
OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 abstract 1
229960001231 choline Drugs 0.000 abstract 1
JSYGRUBHOCKMGQ-UHFFFAOYSA-N dichloramine Chemical compound ClNCl JSYGRUBHOCKMGQ-UHFFFAOYSA-N 0.000 abstract 1
239000003085 diluting agent Substances 0.000 abstract 1
239000008298 dragée Substances 0.000 abstract 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
150000004820 halides Chemical group 0.000 abstract 1
125000005843 halogen group Chemical group 0.000 abstract 1
230000002140 halogenating effect Effects 0.000 abstract 1
238000010438 heat treatment Methods 0.000 abstract 1
229910052739 hydrogen Inorganic materials 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
238000007327 hydrogenolysis reaction Methods 0.000 abstract 1
230000003301 hydrolyzing effect Effects 0.000 abstract 1
239000007788 liquid Substances 0.000 abstract 1
229910052751 metal Chemical group 0.000 abstract 1
239000002184 metal Chemical group 0.000 abstract 1
NALGTKRTIJHBBK-UHFFFAOYSA-N n-(3-chloro-2-methylphenyl)acetamide Chemical compound CC(=O)NC1=CC=CC(Cl)=C1C NALGTKRTIJHBBK-UHFFFAOYSA-N 0.000 abstract 1
230000001590 oxidative effect Effects 0.000 abstract 1
239000000825 pharmaceutical preparation Substances 0.000 abstract 1
LEVJVKGPFAQPOI-UHFFFAOYSA-N phenylmethanone Chemical class O=[C]C1=CC=CC=C1 LEVJVKGPFAQPOI-UHFFFAOYSA-N 0.000 abstract 1
UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 abstract 1
239000000843 powder Substances 0.000 abstract 1
238000002360 preparation method Methods 0.000 abstract 1
150000003254 radicals Chemical group 0.000 abstract 1
230000000552 rheumatic effect Effects 0.000 abstract 1
239000007787 solid Substances 0.000 abstract 1
239000000243 solution Substances 0.000 abstract 1
125000003107 substituted aryl group Chemical group 0.000 abstract 1
239000000725 suspension Substances 0.000 abstract 1
208000024891 symptom Diseases 0.000 abstract 1
239000003826 tablet Substances 0.000 abstract 1
229960004418 trolamine Drugs 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

ES268522A 1961-01-12 1961-06-22 Un procedimiento para la producción de nuevos ácidos antranílicos Expired ES268522A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US8218561A	1961-01-12	1961-01-12

Publications (1)

Publication Number	Publication Date
ES268522A1 true ES268522A1 (es)	1962-04-16

Family

ID=22169584

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES268522A Expired ES268522A1 (es)	1961-01-12	1961-06-22	Un procedimiento para la producción de nuevos ácidos antranílicos

Country Status (8)

Country	Link
BR (1)	BR6130119D0 (es)
CH (2)	CH405348A (es)
DE (1)	DE1149015B (es)
DK (1)	DK105594C (es)
ES (1)	ES268522A1 (es)
FR (2)	FR1457258A (es)
GB (1)	GB984120A (es)
NL (2)	NL266265A (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8717997D0 (en) *	1987-07-29	1987-09-03	Inverni Della Beffa Spa	Derivatives of benzoyloxyacetic acid
IT1288123B1 (it)	1996-09-04	1998-09-10	Nicox Sa	Uso di nitroderivati per l'incontinenza urinaria
CL2014002617A1 (es) *	2014-09-30	2015-01-16	Pontifica Universidad Catolica De Chile	Procedimiento para preparar compuestos derivados de imidazoquinazolina que comprende hacer reaccionar cloruro de n-(2-cianofenil)bencimidoil con etilendiamina o 1,3-diaminopropano a temperatura ambiente.

0
- NL NL123122D patent/NL123122C/xx active
- NL NL266265D patent/NL266265A/xx unknown
1961
- 1961-06-19 BR BR130119/61A patent/BR6130119D0/pt unknown
- 1961-06-22 ES ES268522A patent/ES268522A1/es not_active Expired
- 1961-06-22 DK DK186962AA patent/DK105594C/da active
- 1961-06-22 CH CH1440065A patent/CH405348A/fr unknown
- 1961-06-22 FR FR865810A patent/FR1457258A/fr not_active Expired
- 1961-06-22 CH CH731261A patent/CH401992A/fr unknown
- 1961-06-22 GB GB22726/61A patent/GB984120A/en not_active Expired
- 1961-06-22 DE DEP27408A patent/DE1149015B/de active Pending
- 1961-09-21 FR FR873841A patent/FR1383M/fr active Active

Also Published As

Publication number	Publication date
CH401992A (fr)	1965-11-15
DE1149015B (de)	1963-05-22
FR1383M (fr)	1962-07-02
DK105594C (da)	1966-10-17
NL266265A (es)
NL123122C (es)
FR1457258A (fr)	1966-01-24
GB984120A (en)	1965-02-24
CH405348A (fr)	1966-01-15
BR6130119D0 (pt)	1973-06-07

Publication	Publication Date	Title
US2910488A (en)	1959-10-27	Aniline derivatives
US3655679A (en)	1972-04-11	Certain aryl pyridine carboxylic acid derivatives
JPS5929185B2 (ja)	1984-07-18	フエノ−ル誘導体の製造法
IE36106L (en)	1972-02-19	Isoindoline derivatives
PL84493B1 (es)	1976-04-30
US3658829A (en)	1972-04-25	Phenoxy carboxylic acid derivatives
ES268522A1 (es)	1962-04-16	Un procedimiento para la producción de nuevos ácidos antranílicos
JPS61183286A (ja)	1986-08-15	２‐アルコキシ‐ｎ‐（１‐アザビシクロ〔２，２，２〕オクタン‐３‐イル）アミノベンズアミドの製法
SE7407545L (es)	1974-12-09
GB1453643A (en)	1976-10-27	Bis-benzyl-acetic acid derivatives
JPH0641433B2 (ja)	1994-06-01	ω‐（２’，４’‐ジハロビフエニイル）オキソアルカン酸およびその製法
US4052514A (en)	1977-10-04	Trihalosubstituted biphenylyl propionic acids
GB1418172A (en)	1975-12-17	5-haloalkyl- picolinic acid and process of production thereof
KR890000422A (ko)	1989-03-14	폴리하이드로벤즈[c,d]인돌설폰아미드
US3064006A (en)	1962-11-13	Novel 5-substituted-6-sulfamyl phthalimides
GB1465219A (en)	1977-02-23	Process for the preparation of a phenyl alkonoic acid and its salts
JPS5951542B2 (ja)	1984-12-14	５−フエニル−チアゾリジン−４−オン誘導体の製造方法
JPS59510B2 (ja)	1984-01-07	ピリジンユウドウタイノセイゾウホウ
US3840575A (en)	1974-10-08	Bismuth subcompounds and their methods of preparation
US3994908A (en)	1976-11-30	Substituted acetic acid derivatives and production thereof
GB1341329A (en)	1973-12-19	Indole derivatives process for producing them and compositions containing them
Cavallito et al.	1941	The Action of Halogens on α, β-Unsaturated Ureides
JPH0399065A (ja)	1991-04-24	イミダゾール系化合物の製造方法
JPS6232181B2 (es)	1987-07-13
JPS6032629B2 (ja)	1985-07-29	新規なベンジルピリジン誘導体