TH863B - 2-amino-3- (halobenzoyl) acids - methylphenylacetic ester and salts of these substances. - Google Patents
2-amino-3- (halobenzoyl) acids - methylphenylacetic ester and salts of these substances.Info
- Publication number
- TH863B TH863B TH8201000037A TH8201000037A TH863B TH 863 B TH863 B TH 863B TH 8201000037 A TH8201000037 A TH 8201000037A TH 8201000037 A TH8201000037 A TH 8201000037A TH 863 B TH863 B TH 863B
- Authority
- TH
- Thailand
- Prior art keywords
- amino
- salts
- ester
- substances
- formula
- Prior art date
Links
- 150000002148 esters Chemical class 0.000 title claims abstract 4
- 150000003839 salts Chemical class 0.000 title claims abstract 4
- 239000000126 substance Substances 0.000 title claims abstract 4
- 125000006331 halo benzoyl group Chemical group 0.000 title 1
- 229910052751 metal Inorganic materials 0.000 claims abstract 3
- 239000002184 metal Substances 0.000 claims abstract 3
- 239000002253 acid Substances 0.000 claims abstract 2
- 125000000217 alkyl group Chemical group 0.000 claims abstract 2
- 125000005843 halogen group Chemical group 0.000 claims abstract 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 6
- 230000007062 hydrolysis Effects 0.000 claims 2
- 238000006460 hydrolysis reaction Methods 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 claims 1
- -1 4-fluorobenzoyl Chemical group 0.000 claims 1
- HFLGZTLNWGZCBU-UHFFFAOYSA-N 7-benzoyl-1-methyl-3h-indol-2-one Chemical compound C=12N(C)C(=O)CC2=CC=CC=1C(=O)C1=CC=CC=C1 HFLGZTLNWGZCBU-UHFFFAOYSA-N 0.000 claims 1
- 230000002378 acidificating effect Effects 0.000 claims 1
- 150000001350 alkyl halides Chemical class 0.000 claims 1
- 239000007864 aqueous solution Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 150000002500 ions Chemical class 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 150000004682 monohydrates Chemical class 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- WNCLIUXXSKAOND-UHFFFAOYSA-M sodium;2-[2-amino-3-(4-chlorobenzoyl)-5-methylphenyl]acetate Chemical compound [Na+].CC1=CC(CC([O-])=O)=C(N)C(C(=O)C=2C=CC(Cl)=CC=2)=C1 WNCLIUXXSKAOND-UHFFFAOYSA-M 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 206010059024 Gastrointestinal toxicity Diseases 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- 150000001768 cations Chemical class 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 231100000414 gastrointestinal toxicity Toxicity 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
Abstract
มีการสังเคราะห์ กรด 2-อมิโน-3-(ฮาโลเบนโซอิล)-เมทธิลเฟนนิล อาซีติคชนิดใหม่ เอสเทอร์และเกลือของสารเหล่านี้ ซึ่งมีสูตรดังนี้ สูตร ซึ่ง R เลือกจากกลุ่มซึ่งประกอบด้วยไฮโดรเจนอะตอม อัลคิลที่มี C1-C6 หรืออิออนประจุบวกของโลหะซึ่งใช้ในทางเภสัชกรรมได้ Yคือฮาโลเจนอะตอมและ n คือ เลขจำนวนเต็มตั้งแต่ 1 ถึง 3 สารเหล่านี้แสดงการออกฤทธิ์ต่อต้านการอักเสบ และลดความเจ็บปวดที่ดีเด่นในสัตว์เลือดอุ่นโดยที่มีความเป็นพิษต่อระบบทางเดินอาหารต่ำที่สุด สิทธิบัตรยา 2-amino-3-(halobenzoyl)-methylphenyl acid is synthesized. a new type of acetic The esters and their salts It has the following formula: the formula, in which R can be selected from a group of hydrogen atoms, alkyl containing C1-C6, or a metal cation, which can be used in pharmaceuticals. Y is a halogen atom and n is an integer from 1 to 3. These substances show anti-inflammatory action. and outstanding pain reduction in warm-blooded animals with the lowest gastrointestinal toxicity.
Claims (3)
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TH504A TH504A (en) | 1982-08-13 |
| TH863B true TH863B (en) | 1988-01-18 |
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