NO820073L - Fremgangsmaate for fremstilling av 4-aminobutyramider - Google Patents
Fremgangsmaate for fremstilling av 4-aminobutyramiderInfo
- Publication number
- NO820073L NO820073L NO820073A NO820073A NO820073L NO 820073 L NO820073 L NO 820073L NO 820073 A NO820073 A NO 820073A NO 820073 A NO820073 A NO 820073A NO 820073 L NO820073 L NO 820073L
- Authority
- NO
- Norway
- Prior art keywords
- stated
- nitro
- butyramide
- preparation
- carried out
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 18
- CUSYXOQIPLRISK-UHFFFAOYSA-N 4-nitrobutanamide Chemical compound NC(=O)CCC[N+]([O-])=O CUSYXOQIPLRISK-UHFFFAOYSA-N 0.000 claims abstract description 9
- 238000005984 hydrogenation reaction Methods 0.000 claims abstract description 6
- WCVPFJVXEXJFLB-UHFFFAOYSA-N 4-aminobutanamide Chemical compound NCCCC(N)=O WCVPFJVXEXJFLB-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000003054 catalyst Substances 0.000 claims abstract description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 4
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 claims description 4
- 229910003446 platinum oxide Inorganic materials 0.000 claims description 4
- 238000007098 aminolysis reaction Methods 0.000 claims description 3
- 229910021529 ammonia Inorganic materials 0.000 claims description 3
- 235000019270 ammonium chloride Nutrition 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000007868 Raney catalyst Substances 0.000 claims description 2
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 claims description 2
- 229910000564 Raney nickel Inorganic materials 0.000 claims description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- UBSPKGKFFQKZJB-UHFFFAOYSA-N methyl 4-nitrobutanoate Chemical compound COC(=O)CCC[N+]([O-])=O UBSPKGKFFQKZJB-UHFFFAOYSA-N 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- YKAWOJYVXDCFDP-UHFFFAOYSA-N 3-cyanopropanamide Chemical compound NC(=O)CCC#N YKAWOJYVXDCFDP-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- -1 by aminolysis Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- SSOLNOMRVKKSON-UHFFFAOYSA-N proguanil Chemical compound CC(C)\N=C(/N)N=C(N)NC1=CC=C(Cl)C=C1 SSOLNOMRVKKSON-UHFFFAOYSA-N 0.000 description 1
- 230000000506 psychotropic effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Peptides Or Proteins (AREA)
- Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8100440A FR2497797A1 (fr) | 1981-01-13 | 1981-01-13 | Procede de preparation de l'amino-4 butyramide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO820073L true NO820073L (no) | 1982-07-14 |
Family
ID=9254051
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO820073A NO820073L (no) | 1981-01-13 | 1982-01-12 | Fremgangsmaate for fremstilling av 4-aminobutyramider |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP0056343B1 (ja) |
| JP (1) | JPS57139046A (ja) |
| AT (1) | ATE6933T1 (ja) |
| AU (1) | AU7945582A (ja) |
| DE (1) | DE3260086D1 (ja) |
| DK (1) | DK10082A (ja) |
| ES (1) | ES508656A0 (ja) |
| FI (1) | FI820092L (ja) |
| FR (1) | FR2497797A1 (ja) |
| GR (1) | GR75180B (ja) |
| IE (1) | IE52513B1 (ja) |
| IL (1) | IL64760A0 (ja) |
| NO (1) | NO820073L (ja) |
| NZ (1) | NZ199468A (ja) |
| PT (1) | PT74274A (ja) |
| ZA (1) | ZA82185B (ja) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20120081993A (ko) * | 2009-10-06 | 2012-07-20 | 바이엘 크롭사이언스 아게 | 1,1-디플루오로-2-니트로에탄의 수소화에 의한 2,2-디플루오로에틸아민 유도체의 제조방법 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1225419A (fr) * | 1958-07-29 | 1960-06-30 | Montedison Spa | Procédé pour la préparation de l'amide de l'acide omega-aminocaprylique et produits obtenus par ce procédé |
| DE2316459C2 (de) * | 1973-04-03 | 1982-06-24 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von 1- Nitrobenzol-2-carbonsäure-alkylester-5-carbonsäureamiden |
| DE2319360A1 (de) * | 1973-04-17 | 1974-11-07 | Basf Ag | Verfahren zur herstellung von epsilonaminocapronsaeureamid |
-
1981
- 1981-01-13 FR FR8100440A patent/FR2497797A1/fr active Granted
-
1982
- 1982-01-07 AT AT82400013T patent/ATE6933T1/de not_active IP Right Cessation
- 1982-01-07 EP EP82400013A patent/EP0056343B1/fr not_active Expired
- 1982-01-07 DE DE8282400013T patent/DE3260086D1/de not_active Expired
- 1982-01-12 JP JP57003985A patent/JPS57139046A/ja active Pending
- 1982-01-12 NO NO820073A patent/NO820073L/no unknown
- 1982-01-12 ZA ZA82185A patent/ZA82185B/xx unknown
- 1982-01-12 FI FI820092A patent/FI820092L/fi not_active Application Discontinuation
- 1982-01-12 IL IL64760A patent/IL64760A0/xx unknown
- 1982-01-12 ES ES508656A patent/ES508656A0/es active Granted
- 1982-01-12 PT PT74274A patent/PT74274A/pt unknown
- 1982-01-12 IE IE49/82A patent/IE52513B1/en unknown
- 1982-01-12 DK DK10082A patent/DK10082A/da not_active Application Discontinuation
- 1982-01-12 AU AU79455/82A patent/AU7945582A/en not_active Abandoned
- 1982-01-12 GR GR66987A patent/GR75180B/el unknown
- 1982-01-12 NZ NZ199468A patent/NZ199468A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| FI820092L (fi) | 1982-07-14 |
| ATE6933T1 (de) | 1984-04-15 |
| IE52513B1 (en) | 1987-11-25 |
| IL64760A0 (en) | 1982-03-31 |
| FR2497797B1 (ja) | 1983-12-23 |
| ZA82185B (en) | 1983-01-26 |
| EP0056343A1 (fr) | 1982-07-21 |
| EP0056343B1 (fr) | 1984-04-04 |
| DK10082A (da) | 1982-07-14 |
| NZ199468A (en) | 1984-05-31 |
| ES8502080A1 (es) | 1984-12-01 |
| PT74274A (fr) | 1982-02-01 |
| JPS57139046A (en) | 1982-08-27 |
| ES508656A0 (es) | 1984-12-01 |
| AU7945582A (en) | 1982-07-22 |
| DE3260086D1 (en) | 1984-05-10 |
| GR75180B (ja) | 1984-07-13 |
| FR2497797A1 (fr) | 1982-07-16 |
| IE820049L (en) | 1982-07-13 |
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