JP2006509749A5 - - Google Patents
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- Publication number
- JP2006509749A5 JP2006509749A5 JP2004552856A JP2004552856A JP2006509749A5 JP 2006509749 A5 JP2006509749 A5 JP 2006509749A5 JP 2004552856 A JP2004552856 A JP 2004552856A JP 2004552856 A JP2004552856 A JP 2004552856A JP 2006509749 A5 JP2006509749 A5 JP 2006509749A5
- Authority
- JP
- Japan
- Prior art keywords
- compound
- formula
- alkyl
- benzofuran
- carbamoyl
- Prior art date
- 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.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims 16
- 125000000217 alkyl group Chemical group 0.000 claims 9
- -1 carbocyclyloxy Chemical group 0.000 claims 6
- 239000000651 prodrug Substances 0.000 claims 6
- 229940002612 prodrugs Drugs 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 6
- 239000011780 sodium chloride Substances 0.000 claims 6
- 239000012453 solvate Substances 0.000 claims 6
- 229910052799 carbon Inorganic materials 0.000 claims 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 5
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 3
- 201000010099 disease Diseases 0.000 claims 3
- 125000001475 halogen functional group Chemical group 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000004452 carbocyclyl group Chemical group 0.000 claims 2
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 2
- 230000001404 mediated Effects 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 claims 2
- XCDSRKRYNHJWLJ-UHFFFAOYSA-N 2-[[2-methyl-4-(2-methylpropoxy)-1-benzofuran-6-carbonyl]amino]-1,3-thiazole-5-carboxylic acid Chemical compound C=1C=2OC(C)=CC=2C(OCC(C)C)=CC=1C(=O)NC1=NC=C(C(O)=O)S1 XCDSRKRYNHJWLJ-UHFFFAOYSA-N 0.000 claims 1
- BQZYZYXJDBAODU-UHFFFAOYSA-N 2-methyl-4-(2-methylpropoxy)-N-(1,3-thiazol-2-yl)-1-benzofuran-6-carboxamide Chemical compound C=1C=2OC(C)=CC=2C(OCC(C)C)=CC=1C(=O)NC1=NC=CS1 BQZYZYXJDBAODU-UHFFFAOYSA-N 0.000 claims 1
- KMTJAPUSVPTZRU-UHFFFAOYSA-N 6-[[2-methyl-4-(2-methylpropoxy)-1-benzofuran-6-carbonyl]amino]pyridine-3-carboxylic acid Chemical compound C=1C=2OC(C)=CC=2C(OCC(C)C)=CC=1C(=O)NC1=CC=C(C(O)=O)C=N1 KMTJAPUSVPTZRU-UHFFFAOYSA-N 0.000 claims 1
- MNFLMHZRELRJJT-UHFFFAOYSA-N 6-[[2-methyl-4-(2-thiophen-2-ylethoxy)-1-benzofuran-6-carbonyl]amino]pyridine-3-carboxylic acid Chemical compound C1=C(C(=O)NC=2N=CC(=CC=2)C(O)=O)C=C2OC(C)=CC2=C1OCCC1=CC=CS1 MNFLMHZRELRJJT-UHFFFAOYSA-N 0.000 claims 1
- VQLBNAWDHZEVDB-UHFFFAOYSA-N 6-[[2-methyl-4-[(5-methyl-1,2-oxazol-3-yl)methoxy]-1-benzofuran-6-carbonyl]amino]pyridine-3-carboxylic acid Chemical compound O1C(C)=CC(COC=2C=3C=C(C)OC=3C=C(C=2)C(=O)NC=2N=CC(=CC=2)C(O)=O)=N1 VQLBNAWDHZEVDB-UHFFFAOYSA-N 0.000 claims 1
- JLUHUDOTYQEFPP-UHFFFAOYSA-N 6-[[4-[(2-fluorophenyl)methoxy]-1-benzofuran-6-carbonyl]amino]pyridine-3-carboxylic acid Chemical compound N1=CC(C(=O)O)=CC=C1NC(=O)C1=CC(OCC=2C(=CC=CC=2)F)=C(C=CO2)C2=C1 JLUHUDOTYQEFPP-UHFFFAOYSA-N 0.000 claims 1
- NMKZJHZYESRZDN-UHFFFAOYSA-N 6-[[4-[(2-fluorophenyl)methoxy]-2-methyl-1-benzofuran-6-carbonyl]amino]pyridine-3-carboxylic acid Chemical compound C1=C(C(=O)NC=2N=CC(=CC=2)C(O)=O)C=C2OC(C)=CC2=C1OCC1=CC=CC=C1F NMKZJHZYESRZDN-UHFFFAOYSA-N 0.000 claims 1
- HRGYRYSSHIVOJP-UHFFFAOYSA-N 6-[[4-[(5-methyl-1,2-oxazol-3-yl)methoxy]-1-benzofuran-6-carbonyl]amino]pyridine-3-carboxylic acid Chemical compound O1C(C)=CC(COC=2C=3C=COC=3C=C(C=2)C(=O)NC=2N=CC(=CC=2)C(O)=O)=N1 HRGYRYSSHIVOJP-UHFFFAOYSA-N 0.000 claims 1
- 241000124008 Mammalia Species 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 125000004185 ester group Chemical group 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 238000005755 formation reaction Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000006239 protecting group Chemical group 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0226930.6A GB0226930D0 (en) | 2002-11-19 | 2002-11-19 | Chemical compounds |
| PCT/GB2003/004919 WO2004046139A1 (en) | 2002-11-19 | 2003-11-13 | Benzofuran derivates, process for their preparation and intermediates thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006509749A JP2006509749A (ja) | 2006-03-23 |
| JP2006509749A5 true JP2006509749A5 (US06894165-20050517-C00155.png) | 2006-10-19 |
| JP4511939B2 JP4511939B2 (ja) | 2010-07-28 |
Family
ID=9948089
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004552856A Expired - Fee Related JP4511939B2 (ja) | 2002-11-19 | 2003-11-13 | ベンゾフラン誘導体、その製造方法およびその中間体 |
Country Status (9)
Families Citing this family (40)
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| SE0102299D0 (sv) | 2001-06-26 | 2001-06-26 | Astrazeneca Ab | Compounds |
| GB0226930D0 (en) | 2002-11-19 | 2002-12-24 | Astrazeneca Ab | Chemical compounds |
| GB0226931D0 (en) | 2002-11-19 | 2002-12-24 | Astrazeneca Ab | Chemical compounds |
| GB0328178D0 (en) * | 2003-12-05 | 2004-01-07 | Astrazeneca Ab | Compounds |
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| TW200600086A (en) * | 2004-06-05 | 2006-01-01 | Astrazeneca Ab | Chemical compound |
| TW200714597A (en) * | 2005-05-27 | 2007-04-16 | Astrazeneca Ab | Chemical compounds |
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| MX348131B (es) | 2011-02-25 | 2017-05-26 | Merck Sharp & Dohme | Novedosos derivados de azabencimidazol ciclico utiles como agentes antidiabeticos. |
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| US9840512B2 (en) | 2013-02-22 | 2017-12-12 | Merck Sharp & Dohme Corp. | Antidiabetic bicyclic compounds |
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| WO2015051496A1 (en) | 2013-10-08 | 2015-04-16 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
| CN107619392B (zh) * | 2016-07-15 | 2021-01-01 | 西华大学 | 1h-吲唑-4-醚类化合物及其作为ido抑制剂的用途 |
| WO2018106518A1 (en) | 2016-12-06 | 2018-06-14 | Merck Sharp & Dohme Corp. | Antidiabetic heterocyclic compounds |
| WO2018118670A1 (en) | 2016-12-20 | 2018-06-28 | Merck Sharp & Dohme Corp. | Antidiabetic spirochroman compounds |
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2002
- 2002-11-19 GB GBGB0226930.6A patent/GB0226930D0/en not_active Ceased
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2003
- 2003-11-13 ES ES03773852T patent/ES2293045T3/es not_active Expired - Lifetime
- 2003-11-13 US US10/534,650 patent/US7709505B2/en not_active Expired - Fee Related
- 2003-11-13 DE DE60317562T patent/DE60317562T2/de not_active Expired - Lifetime
- 2003-11-13 WO PCT/GB2003/004919 patent/WO2004046139A1/en active IP Right Grant
- 2003-11-13 AT AT03773852T patent/ATE378332T1/de not_active IP Right Cessation
- 2003-11-13 AU AU2003282234A patent/AU2003282234A1/en not_active Abandoned
- 2003-11-13 EP EP03773852A patent/EP1578745B1/en not_active Expired - Lifetime
- 2003-11-13 JP JP2004552856A patent/JP4511939B2/ja not_active Expired - Fee Related
