ATE407112T1 - Verfahren zur herstellung von r-(-)-n, alpha- dimethylphenethylamin (levmetamphetamin) oder s- (+)-n, alpha-dimethylphenethylamin (metamphetamin) aus d-ephedrin bzw. l-ephedrin - Google Patents
Verfahren zur herstellung von r-(-)-n, alpha- dimethylphenethylamin (levmetamphetamin) oder s- (+)-n, alpha-dimethylphenethylamin (metamphetamin) aus d-ephedrin bzw. l-ephedrinInfo
- Publication number
- ATE407112T1 ATE407112T1 AT04821403T AT04821403T ATE407112T1 AT E407112 T1 ATE407112 T1 AT E407112T1 AT 04821403 T AT04821403 T AT 04821403T AT 04821403 T AT04821403 T AT 04821403T AT E407112 T1 ATE407112 T1 AT E407112T1
- Authority
- AT
- Austria
- Prior art keywords
- formula
- ephedrine
- alpha
- dimethylphenethylamin
- levmetamphetamin
- Prior art date
Links
- MYWUZJCMWCOHBA-SECBINFHSA-N levmetamfetamine Chemical compound CN[C@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-SECBINFHSA-N 0.000 title abstract 4
- 229960002179 ephedrine Drugs 0.000 title 2
- 238000004519 manufacturing process Methods 0.000 title 1
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 abstract 2
- KWGRBVOPPLSCSI-PSASIEDQSA-N (1s,2r)-2-(methylamino)-1-phenylpropan-1-ol Chemical compound CN[C@H](C)[C@@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-PSASIEDQSA-N 0.000 abstract 2
- 229950007554 levmetamfetamine Drugs 0.000 abstract 2
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 abstract 2
- 229960001252 methamphetamine Drugs 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 229910000564 Raney nickel Inorganic materials 0.000 abstract 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 abstract 1
- 238000005903 acid hydrolysis reaction Methods 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 abstract 1
- 238000006392 deoxygenation reaction Methods 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/62—Preparation of compounds containing amino groups bound to a carbon skeleton by cleaving carbon-to-nitrogen, sulfur-to-nitrogen, or phosphorus-to-nitrogen bonds, e.g. hydrolysis of amides, N-dealkylation of amines or quaternary ammonium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/IN2004/000398 WO2006067794A1 (en) | 2004-12-22 | 2004-12-22 | A PROCESS FOR THE PREPARATION OF R-(-)-N, α-DIMETHYLPHENETHYLAMINE (LEVMETAMFETAMINE) OR S-(+)-N, α-DIMETHYLPHENETHYLAMINE (METHAMPHETAMINE) FROM d-EPHEDRINE OR L-EPHEDRINE RESPECTIVELY |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE407112T1 true ATE407112T1 (de) | 2008-09-15 |
Family
ID=34965239
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT04821403T ATE407112T1 (de) | 2004-12-22 | 2004-12-22 | Verfahren zur herstellung von r-(-)-n, alpha- dimethylphenethylamin (levmetamphetamin) oder s- (+)-n, alpha-dimethylphenethylamin (metamphetamin) aus d-ephedrin bzw. l-ephedrin |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20080293971A1 (de) |
| EP (1) | EP1828105B1 (de) |
| JP (1) | JP2008525428A (de) |
| AT (1) | ATE407112T1 (de) |
| DE (1) | DE602004016401D1 (de) |
| ES (1) | ES2314494T3 (de) |
| WO (1) | WO2006067794A1 (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110066220A (zh) * | 2019-05-29 | 2019-07-30 | 深圳市茵诺圣生物科技有限公司 | 一种司来吉兰的制备方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6399828B1 (en) * | 2001-10-29 | 2002-06-04 | Boehringer Ingelheim Chemicals, Inc. | Preparation of amphetamines from phenylpropanolamines |
-
2004
- 2004-12-22 US US11/722,494 patent/US20080293971A1/en not_active Abandoned
- 2004-12-22 DE DE602004016401T patent/DE602004016401D1/de not_active Expired - Lifetime
- 2004-12-22 JP JP2007547792A patent/JP2008525428A/ja active Pending
- 2004-12-22 WO PCT/IN2004/000398 patent/WO2006067794A1/en not_active Ceased
- 2004-12-22 ES ES04821403T patent/ES2314494T3/es not_active Expired - Lifetime
- 2004-12-22 EP EP04821403A patent/EP1828105B1/de not_active Expired - Lifetime
- 2004-12-22 AT AT04821403T patent/ATE407112T1/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1828105B1 (de) | 2008-09-03 |
| ES2314494T3 (es) | 2009-03-16 |
| EP1828105A1 (de) | 2007-09-05 |
| US20080293971A1 (en) | 2008-11-27 |
| DE602004016401D1 (de) | 2008-10-16 |
| JP2008525428A (ja) | 2008-07-17 |
| WO2006067794A1 (en) | 2006-06-29 |
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Legal Events
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|---|---|---|---|
| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |