KR890009908A - N-(2-클로로벤질)-2-(2-티에닐)에틸아민의 제조방법 - Google Patents
N-(2-클로로벤질)-2-(2-티에닐)에틸아민의 제조방법 Download PDFInfo
- Publication number
- KR890009908A KR890009908A KR1019880016378A KR880016378A KR890009908A KR 890009908 A KR890009908 A KR 890009908A KR 1019880016378 A KR1019880016378 A KR 1019880016378A KR 880016378 A KR880016378 A KR 880016378A KR 890009908 A KR890009908 A KR 890009908A
- Authority
- KR
- South Korea
- Prior art keywords
- chlorobenzyl
- ethylamine
- thienyl
- molar ratio
- catalyst
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 10
- KEOKHDKWKYGPGO-UHFFFAOYSA-N n-[(2-chlorophenyl)methyl]-2-thiophen-2-ylethanamine Chemical compound ClC1=CC=CC=C1CNCCC1=CC=CS1 KEOKHDKWKYGPGO-UHFFFAOYSA-N 0.000 title claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 239000003054 catalyst Substances 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- KDDNKZCVYQDGKE-UHFFFAOYSA-N (2-chlorophenyl)methanamine Chemical compound NCC1=CC=CC=C1Cl KDDNKZCVYQDGKE-UHFFFAOYSA-N 0.000 claims 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical group [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- CLSHQIDDCJTHAJ-UHFFFAOYSA-N 2-thienylacetonitrile Chemical compound N#CCC1=CC=CS1 CLSHQIDDCJTHAJ-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 239000007868 Raney catalyst Substances 0.000 claims 1
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical group [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 claims 1
- 229910000564 Raney nickel Inorganic materials 0.000 claims 1
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims 1
- 238000005984 hydrogenation reaction Methods 0.000 claims 1
- 229910052763 palladium Inorganic materials 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
- C07D333/20—Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Plural Heterocyclic Compounds (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (9)
- 수소화 촉매의 존재하에서 2-티오펜 아세토니트릴을 2-클로로 벤질아민 및 수소와 반응시키는 것을 특징으로 하는 N-(2-클로로벤질)-2-(2-티에닐)에틸아민의 제조방법.
- 제1항에 있어서, 반응조의 수소 압력이 1-10MPa인 것을 특징으로 하는 방법.
- 제2항에 있어서, 수소 압력이 2.5-7MPa인 것을 특징으로 하는 방법.
- 제1항에 있어서, 반응이 80℃ 미만에서 이루어지는 것을 특징으로 하는 방법.
- 제4항에 있어서, 온도가 40-60℃인 것을 특징으로 하는 방법.
- 제1항에 있어서, 알콜을 용매로하여 반응이 이루어지는 것을 특징으로 하는 방법.
- 제1항에 있어서, 2-클로로 벤질아민과 2-티오펜 아세토리트릴의 몰비가 1-5인 것을 특징으로 하는 방법.
- 제7항에 있어서, 촉매가 라니 니켈이고 상기 몰비가 2-4인 것을 특징으로 하는 방법.
- 제7항에 있어서, 촉매가 팔라듐이고 상기 몰비가 1-2인 것을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8717755 | 1987-12-18 | ||
FR8717755A FR2624860B1 (fr) | 1987-12-18 | 1987-12-18 | Procede de preparation de la n-(chloro-2 benzyl) (thienyl-2)-2 ethylamine |
Publications (2)
Publication Number | Publication Date |
---|---|
KR890009908A true KR890009908A (ko) | 1989-08-04 |
KR960014798B1 KR960014798B1 (en) | 1996-10-19 |
Family
ID=9358062
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR88016378A KR960014798B1 (en) | 1987-12-18 | 1988-12-08 | Process for the preparation of n-(2-chloro-benzyl)(2-thienyl)-2-ethylamine |
Country Status (10)
Country | Link |
---|---|
US (1) | US4873343A (ko) |
EP (1) | EP0321349B1 (ko) |
JP (1) | JP2664450B2 (ko) |
KR (1) | KR960014798B1 (ko) |
AT (1) | ATE74918T1 (ko) |
CA (1) | CA1329212C (ko) |
DE (1) | DE3870183D1 (ko) |
ES (1) | ES2032218T3 (ko) |
FR (1) | FR2624860B1 (ko) |
PT (1) | PT89228B (ko) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2664596B1 (fr) * | 1990-07-10 | 1994-06-10 | Sanofi Sa | Procede de preparation d'un derive n-phenylacetique de tetrahydrothieno [3,2-c] pyridine et son intermediaire de synthese. |
US6043368A (en) * | 1996-09-04 | 2000-03-28 | Poli Industria Chimica, S.P.A. | Method of making thieno-pyridine derivatives |
FR2760456B1 (fr) * | 1997-03-05 | 2000-05-12 | Sanofi Sa | Procede de preparation de derives de 2-thienyl-ethylamine |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2300090A1 (fr) * | 1975-02-07 | 1976-09-03 | Parcor | Procede de preparation de derives de la thienopyridine |
FR2508455A1 (fr) * | 1981-06-30 | 1982-12-31 | Sanofi Sa | Procede de preparation de derives des (thienyl-2)- et (thienyl-3)-2 ethylamines |
FR2608607B1 (fr) * | 1986-12-23 | 1989-04-28 | Sanofi Sa | Procede de preparation de thienylethylamines et dithienylethylamines ainsi obtenues |
-
1987
- 1987-12-18 FR FR8717755A patent/FR2624860B1/fr not_active Expired - Fee Related
-
1988
- 1988-11-23 US US07/275,369 patent/US4873343A/en not_active Expired - Lifetime
- 1988-12-05 CA CA000584974A patent/CA1329212C/en not_active Expired - Lifetime
- 1988-12-08 KR KR88016378A patent/KR960014798B1/ko not_active IP Right Cessation
- 1988-12-15 PT PT89228A patent/PT89228B/pt not_active IP Right Cessation
- 1988-12-15 EP EP88403198A patent/EP0321349B1/fr not_active Expired - Lifetime
- 1988-12-15 AT AT88403198T patent/ATE74918T1/de not_active IP Right Cessation
- 1988-12-15 ES ES198888403198T patent/ES2032218T3/es not_active Expired - Lifetime
- 1988-12-15 JP JP63319325A patent/JP2664450B2/ja not_active Expired - Lifetime
- 1988-12-15 DE DE8888403198T patent/DE3870183D1/de not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
DE3870183D1 (de) | 1992-05-21 |
KR960014798B1 (en) | 1996-10-19 |
PT89228A (pt) | 1989-12-29 |
JP2664450B2 (ja) | 1997-10-15 |
PT89228B (pt) | 1993-07-30 |
JPH01197478A (ja) | 1989-08-09 |
US4873343A (en) | 1989-10-10 |
ES2032218T3 (es) | 1993-01-16 |
ATE74918T1 (de) | 1992-05-15 |
CA1329212C (en) | 1994-05-03 |
EP0321349A1 (fr) | 1989-06-21 |
FR2624860A1 (fr) | 1989-06-23 |
EP0321349B1 (fr) | 1992-04-15 |
FR2624860B1 (fr) | 1990-06-01 |
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