ES415678A1 - Un procedimiento para la preparacion de nuevos derivados deoxazolopiridinas. - Google Patents
Un procedimiento para la preparacion de nuevos derivados deoxazolopiridinas.Info
- Publication number
- ES415678A1 ES415678A1 ES415678A ES415678A ES415678A1 ES 415678 A1 ES415678 A1 ES 415678A1 ES 415678 A ES415678 A ES 415678A ES 415678 A ES415678 A ES 415678A ES 415678 A1 ES415678 A1 ES 415678A1
- Authority
- ES
- Spain
- Prior art keywords
- see formula
- amino
- lower alkyl
- group
- conversion
- 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.)
- Expired
Links
- 238000000034 method Methods 0.000 title abstract 3
- 238000002360 preparation method Methods 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 11
- 238000006243 chemical reaction Methods 0.000 abstract 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 125000003545 alkoxy group Chemical group 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- -1 methylenedioxy group Chemical group 0.000 abstract 4
- 125000004385 trihaloalkyl group Chemical group 0.000 abstract 4
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000004423 acyloxy group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 150000003254 radicals Chemical class 0.000 abstract 2
- 229910052717 sulfur Chemical group 0.000 abstract 2
- 239000011593 sulfur Chemical group 0.000 abstract 2
- 125000003396 thiol group Chemical class [H]S* 0.000 abstract 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- BFPLMTPHDFFMTG-UHFFFAOYSA-N [1,3]oxazolo[5,4-b]pyridine Chemical class C1=CN=C2OC=NC2=C1 BFPLMTPHDFFMTG-UHFFFAOYSA-N 0.000 abstract 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 abstract 1
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 1
- 125000005036 alkoxyphenyl group Chemical group 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
Landscapes
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US26289872A | 1972-06-14 | 1972-06-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES415678A1 true ES415678A1 (es) | 1976-10-01 |
Family
ID=22999543
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES415678A Expired ES415678A1 (es) | 1972-06-14 | 1973-06-07 | Un procedimiento para la preparacion de nuevos derivados deoxazolopiridinas. |
Country Status (9)
| Country | Link |
|---|---|
| ES (1) | ES415678A1 (forum.php) |
| HU (1) | HU166455B (forum.php) |
| IE (1) | IE37768B1 (forum.php) |
| IL (1) | IL42422A (forum.php) |
| NO (1) | NO143535C (forum.php) |
| PH (1) | PH14641A (forum.php) |
| RO (1) | RO72886A (forum.php) |
| SU (1) | SU644386A3 (forum.php) |
| YU (1) | YU154673A (forum.php) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8907093B2 (en) * | 2011-07-07 | 2014-12-09 | Sanofi | Carboxylic acid derivatives having an oxazolo[4,5-c]pyridine ring |
| US8580816B2 (en) * | 2011-07-07 | 2013-11-12 | Sanofi | Carboxylic acid derivatives having an oxazolo[5,4-b]pyridine ring |
| CN107759614B (zh) * | 2016-08-16 | 2023-01-24 | 中国科学院上海药物研究所 | 一类噁唑并吡啶季铵盐类化合物、其制备方法及用途 |
-
1973
- 1973-05-29 NO NO223073A patent/NO143535C/no unknown
- 1973-06-01 IL IL42422A patent/IL42422A/xx unknown
- 1973-06-07 IE IE91973A patent/IE37768B1/xx unknown
- 1973-06-07 ES ES415678A patent/ES415678A1/es not_active Expired
- 1973-06-08 RO RO7384186A patent/RO72886A/ro unknown
- 1973-06-08 YU YU154673A patent/YU154673A/xx unknown
- 1973-06-12 HU HUME001638 patent/HU166455B/hu unknown
- 1973-06-13 SU SU731932096A patent/SU644386A3/ru active
-
1975
- 1975-06-04 PH PH14691A patent/PH14641A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IE37768B1 (en) | 1977-10-12 |
| RO72886A (ro) | 1981-09-24 |
| SU644386A3 (ru) | 1979-01-25 |
| NO143535C (no) | 1981-03-04 |
| IL42422A (en) | 1978-12-17 |
| PH14641A (en) | 1981-10-12 |
| YU154673A (en) | 1982-06-18 |
| IE37768L (en) | 1973-12-14 |
| NO143535B (no) | 1980-11-24 |
| IL42422A0 (en) | 1973-08-29 |
| HU166455B (forum.php) | 1975-03-28 |
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