ES330211A1 - Procedimiento para la obtencion de derivados de la tebaina y oripavina - Google Patents
Procedimiento para la obtencion de derivados de la tebaina y oripavinaInfo
- Publication number
- ES330211A1 ES330211A1 ES0330211A ES330211A ES330211A1 ES 330211 A1 ES330211 A1 ES 330211A1 ES 0330211 A ES0330211 A ES 0330211A ES 330211 A ES330211 A ES 330211A ES 330211 A1 ES330211 A1 ES 330211A1
- Authority
- ES
- Spain
- Prior art keywords
- group
- substituted
- carbon atoms
- atom
- aryl
- 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 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 7
- 125000003277 amino group Chemical group 0.000 abstract 4
- 125000004104 aryloxy group Chemical group 0.000 abstract 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- -1 phenacyl group Chemical group 0.000 abstract 4
- 125000002723 alicyclic group Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000000304 alkynyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 125000003107 substituted aryl group Chemical group 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 101100294102 Caenorhabditis elegans nhr-2 gene Proteins 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 150000001721 carbon Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 150000003254 radicals Chemical class 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- ZKLXUUYLEHCAMF-UUWFMWQGSA-N Oripavine Chemical compound C([C@@H](N(CC1)C)C2=CC=C3OC)C4=CC=C(O)C5=C4[C@@]21[C@H]3O5 ZKLXUUYLEHCAMF-UUWFMWQGSA-N 0.000 abstract 1
- ZKLXUUYLEHCAMF-UHFFFAOYSA-N Oripavine Natural products COC1=CC=C2C(N(CC3)C)CC4=CC=C(O)C5=C4C23C1O5 ZKLXUUYLEHCAMF-UHFFFAOYSA-N 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 1
- 125000001539 acetonyl group Chemical group [H]C([H])([H])C(=O)C([H])([H])* 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 abstract 1
- FQXXSQDCDRQNQE-VMDGZTHMSA-N thebaine Chemical class C([C@@H](N(CC1)C)C2=CC=C3OC)C4=CC=C(OC)C5=C4[C@@]21[C@H]3O5 FQXXSQDCDRQNQE-VMDGZTHMSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D489/00—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula:
- C07D489/09—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: containing 4aH-8, 9 c-Iminoethano- phenanthro [4, 5-b, c, d] furan ring systems condensed with carbocyclic rings or ring systems
- C07D489/10—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: containing 4aH-8, 9 c-Iminoethano- phenanthro [4, 5-b, c, d] furan ring systems condensed with carbocyclic rings or ring systems with a bridge between positions 6 and 14
- C07D489/12—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: containing 4aH-8, 9 c-Iminoethano- phenanthro [4, 5-b, c, d] furan ring systems condensed with carbocyclic rings or ring systems with a bridge between positions 6 and 14 the bridge containing only two carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB34840/65A GB1136764A (en) | 1965-08-13 | 1965-08-13 | Derivatives of thebaine and oripavine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES330211A1 true ES330211A1 (es) | 1967-06-01 |
Family
ID=10370551
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0330211A Expired ES330211A1 (es) | 1965-08-13 | 1966-08-12 | Procedimiento para la obtencion de derivados de la tebaina y oripavina |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US3464994A (es) |
| AT (1) | AT281304B (es) |
| BE (1) | BE685406A (es) |
| BR (1) | BR6682051D0 (es) |
| DE (1) | DE1620210A1 (es) |
| ES (1) | ES330211A1 (es) |
| FR (2) | FR6062M (es) |
| GB (1) | GB1136764A (es) |
| LU (1) | LU51753A1 (es) |
| NL (1) | NL6611414A (es) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3520892A (en) * | 1967-03-17 | 1970-07-21 | American Home Prod | 6-deoxy-7,8-dihydromorphine derivatives |
| DE2230154A1 (de) * | 1972-06-21 | 1974-01-17 | Boehringer Sohn Ingelheim | N-(heteroaryl-methyl)-6,14-endoaetheno7alpha-hydroxyalkyl-tetrahydro-nororipavine und -thebaine, deren hydrierungsprodukte und saeureadditionssalze sowie verfahren zu deren herstellung |
| JP5252391B2 (ja) * | 2008-02-21 | 2013-07-31 | 学校法人北里研究所 | オキサビシクロ［２．２．２］オクタンを有するモルヒナン誘導体およびその医薬用途 |
| PL2326651T3 (pl) * | 2008-07-30 | 2014-05-30 | Purdue Pharma Lp | Analogi buprenorfiny |
| EA201390422A1 (ru) | 2010-09-21 | 2014-01-30 | Пердью Фарма Л.П. | Бупренорфиновые аналоги |
| TW201434842A (zh) | 2012-12-07 | 2014-09-16 | Purdue Pharma Lp | 丁基原啡因（ｂｕｐｒｅｎｏｒｐｈｉｎｅ）類似物類 |
| US8969358B2 (en) | 2013-03-15 | 2015-03-03 | Purdue Pharma L.P. | Buprenorphine analogs |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3285914A (en) * | 1964-06-11 | 1966-11-15 | Smith Kline French Lab | 3-n-substituted derivatives of oripavine and thebaine |
| GB1116595A (en) * | 1964-07-08 | 1968-06-06 | Reckitt & Sons Ltd | Codeine and morphine derivatives |
| US3318885A (en) * | 1965-07-21 | 1967-05-09 | American Cyanamid Co | Substituted 6-amino-6, 14-endoethen-ocodides and morphides |
-
1965
- 1965-08-13 GB GB34840/65A patent/GB1136764A/en not_active Expired
-
1966
- 1966-08-11 BE BE685406D patent/BE685406A/xx unknown
- 1966-08-11 BR BR182051/66A patent/BR6682051D0/pt unknown
- 1966-08-11 LU LU51753A patent/LU51753A1/xx unknown
- 1966-08-12 DE DE19661620210 patent/DE1620210A1/de active Pending
- 1966-08-12 ES ES0330211A patent/ES330211A1/es not_active Expired
- 1966-08-12 AT AT774566A patent/AT281304B/de not_active IP Right Cessation
- 1966-08-12 FR FR73053A patent/FR6062M/fr not_active Expired
- 1966-08-12 NL NL6611414A patent/NL6611414A/xx unknown
- 1966-11-09 FR FR83040A patent/FR1500605A/fr not_active Expired
-
1968
- 1968-05-16 US US729505A patent/US3464994A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AT281304B (de) | 1970-05-11 |
| NL6611414A (es) | 1967-02-14 |
| US3464994A (en) | 1969-09-02 |
| LU51753A1 (es) | 1966-10-11 |
| BE685406A (es) | 1967-01-16 |
| FR6062M (es) | 1968-05-27 |
| BR6682051D0 (pt) | 1973-10-25 |
| DE1620210A1 (de) | 1970-03-05 |
| GB1136764A (en) | 1968-12-18 |
| FR1500605A (fr) | 1967-11-03 |
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