TH310A - Pyridil Submitited 2,3-dihydroimidaso [2,1-b] thiazole - Google Patents
Pyridil Submitited 2,3-dihydroimidaso [2,1-b] thiazoleInfo
- Publication number
- TH310A TH310A TH7901000002A TH7901000002A TH310A TH 310 A TH310 A TH 310A TH 7901000002 A TH7901000002 A TH 7901000002A TH 7901000002 A TH7901000002 A TH 7901000002A TH 310 A TH310 A TH 310A
- Authority
- TH
- Thailand
- Prior art keywords
- piridil
- thiazole
- fluorophenyl
- dihydroimidazo
- acids
- Prior art date
Links
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 title claims 2
- PIINXYKJQGMIOZ-UHFFFAOYSA-N 1,2-dipyridin-2-ylethane-1,2-dione Chemical compound C=1C=CC=NC=1C(=O)C(=O)C1=CC=CC=N1 PIINXYKJQGMIOZ-UHFFFAOYSA-N 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000005977 Ethylene Substances 0.000 claims abstract 2
- 239000002253 acid Substances 0.000 claims 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 3
- 150000007513 acids Chemical class 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 238000007596 consolidation process Methods 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- 125000002346 iodo group Chemical group I* 0.000 claims 1
- 239000007800 oxidant agent Substances 0.000 claims 1
- 125000001174 sulfone group Chemical class 0.000 claims 1
- 150000003462 sulfoxides Chemical class 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- 230000003356 anti-rheumatic effect Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000036039 immunity Effects 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 abstract 1
- 230000009257 reactivity Effects 0.000 abstract 1
Abstract
5-(4-พิริดิล)-6-(4-ฟลูออโรเฟนิล)-2,3-ไดไฮโดรอิมิดาโซ[2,1-บี] ไธอะโซล มีฤทธิ์ต่อต้านโรคข้ออักเสบและมีฤทธิ์ควบ คุมการเกิดภูมิคุ้มกันอย่างเห็นได้ชัดเมื่อเทียบกับไอโซเ มอร์สลับตำแหน่ง -5, 6 ของมัน สารประกอบนี้เตรียมโดยให้ 4-(4-พิริดิล)-5-(4-ฟลูออโรเฟนิล)-2-เมอร์แคพโทอิมิดาโซล ทำปฏิกิริยากับเอธิลีน ไดเฮไลด์ ที่ว่องไว แล้วแยกสารผสม ของไอโซเมอร์ของผลิตภัณฑ์ สิทธิบัตรยา 5- (4- piridil) -6- (4- fluorophenyl) -2,3-dihydroimidazo [2,1-b] thiazole has anti-rheumatic activity. Inflammation and a concurrent effect Obviously control immunity compared to iso Mor switches its -5, 6 positions. This compound is prepared by giving 4- (4- piridil) -5- (4- fluorophenyl) -2-mercaptoimidazole Reacts with reactivity with ethylene dihylide and separate mixtures. Of isomers of pharmaceutical patent products
Claims (1)
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TH310A true TH310A (en) | 1982-05-11 |
| TH1391B TH1391B (en) | 1989-06-09 |
Family
ID=
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