KR900016119A - 치환 에텐류의 제조 방법 - Google Patents
치환 에텐류의 제조 방법 Download PDFInfo
- Publication number
- KR900016119A KR900016119A KR1019900004645A KR900004645A KR900016119A KR 900016119 A KR900016119 A KR 900016119A KR 1019900004645 A KR1019900004645 A KR 1019900004645A KR 900004645 A KR900004645 A KR 900004645A KR 900016119 A KR900016119 A KR 900016119A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- substituted
- general formula
- compound
- alkyl group
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims 4
- 238000000034 method Methods 0.000 claims 13
- 150000001875 compounds Chemical class 0.000 claims 8
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims 4
- 239000002168 alkylating agent Substances 0.000 claims 4
- 229940100198 alkylating agent Drugs 0.000 claims 4
- 150000001412 amines Chemical class 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- 150000003973 alkyl amines Chemical class 0.000 claims 3
- 125000005842 heteroatom Chemical group 0.000 claims 3
- -1 N, N-dimethylaminomethyl Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 239000012022 methylating agents Substances 0.000 claims 2
- ULOTWPOKIYOEQN-UHFFFAOYSA-N 2-nitroethanedithioic acid Chemical compound [O-][N+](=O)CC(S)=S ULOTWPOKIYOEQN-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical group COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 claims 1
- KCIDZIIHRGYJAE-YGFYJFDDSA-L dipotassium;[(2r,3r,4s,5r,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] phosphate Chemical class [K+].[K+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@H]1O KCIDZIIHRGYJAE-YGFYJFDDSA-L 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N mono-methylamine Natural products NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims 1
- YQFHPXZGXNYYLD-UHFFFAOYSA-N n-methyl-1-methylsulfanyl-2-nitroethenamine Chemical compound CNC(SC)=C[N+]([O-])=O YQFHPXZGXNYYLD-UHFFFAOYSA-N 0.000 claims 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 1
- VMXUWOKSQNHOCA-LCYFTJDESA-N ranitidine Chemical compound [O-][N+](=O)/C=C(/NC)NCCSCC1=CC=C(CN(C)C)O1 VMXUWOKSQNHOCA-LCYFTJDESA-N 0.000 claims 1
- 229960000620 ranitidine Drugs 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
- C07D317/58—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/22—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of hydropolysulfides or polysulfides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
- C07C323/24—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/27—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and unsaturated
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Catalysts (AREA)
- Luminescent Compositions (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Underground Structures, Protecting, Testing And Restoring Foundations (AREA)
- Ultra Sonic Daignosis Equipment (AREA)
Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (15)
- C1-4직쇄 제1급 알킬아민 및 사슬 내에 이형 원자를 함유하는 치환직쇄 제1급 알킬아민으로부터 선택된 제1급 알킬아민을 니트로디티오 아세트산의 이칼륨염과 반응시키는 것이 특징인 하기 일반식(I)의 칼륨염의 제조 방법.상기 식에서, R1은 직쇄 C1-4알킬기 또는 사슬 내에 이형 원자를 함유하는 치환 직쇄 알킬기는 나타낸다.
- 제1항에 있어서, 상기 아민이 메틸아민인 것이 특징인 방법.
- 제1항 또는 제2항에 있어서, 용매로서 물을 사용하는 것이 특징인 방법.
- 하기 일반식(I)의 화합물을 적합한 알킬화제와 반응시키는 것이 특징인 하기 일반식(I)의 N-치환-1-알킬티오-2-니트로 에텐아민의 제조 방법.상기 식에서, R1은 직쇄 C1-4알킬기 또는 사슬 내에 이형 원자를 함유하는 치환 직쇄 알킬기를 나타내고, R2은C1-4알킬기를 나타낸다.
- 제4항에 있어서, 제1항에 정의한 상기 일반식(I)의 화합물을 제1항 내지 제3항중 어느 하나의 항에 의한 제조 방법으로 제조하고, 이어서 상기 일반식(I)의 화합물을 적합한 알킬화제와 반응시켜서 상기 일반식(II)의 N-치환-1-알킬티오-2-니트로에텐아민을 얻는 것이 특징인 상기 일반식(II)의 N-치환-1-알킬티오-2-니트로에텐아민의 제조방법.
- 제4항 또는 제5항에 있어서, 알킬화제와 반응시키는 상기 반응을 동일반응조 내에서 상기 일반식(I)의 화합물 상에서 수행하는 것이 특징인 방법.
- 제4항 내지 제6항 중 어느 하나의 항에 있어서, 상기 알킬화제가 메틸화제인 것이 특징인 방법.
- 제7항에 있어서, 상기 메틸화제가 디메틸 슐페이트인 것이 특징인 방법.
- 제4항 내지 제8항중 어느 하나의 항에 있어서, 상기 일킬화를 상전이제의 존재 하에 수행하는 것이 특징인 방법.
- 제4항 내지 제9항 중 어느 하나의 항에 있어서, R1및 R2가 둘다 메틸기인 상기 일반식(II)의 화합물을 제조하는 것이 특징인 방법.
- 제4항에 정의한 것과 같은 상기 일반식(II)의 N-치환-1-알킬티오-2-니트로에텐아민을 제5항 내지 제10항 중 어느 하나의 항에 의한 방법으로 제조하고, 이어서 상기 일반식(II)의 화합물을 적절한 아민과 반응시키는 것이 특징인 라니티딘의 제조 방법.
- 제11항에 있어서, 상기 아민이 2-[5-(N,N-디메틸아미노메틸)-2-푸란메틸티오]에틸아민인 것이 특징인 방법.
- 제12항에 있어서, 상기 일반식(II)의 화합물이 N-메틸-1-메틸티오-2-니트로에텐아민인 것이 특징인 방법.
- 제1항에 있어서, 상기 아민이 2-[5-(N,N-디메틸아미노메틸)-2-푸란메틸티오]에틸아민인 것이 특징인 방법.
- 하기 일반식으로 정의되는 신규 중간체 화합물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB898907700A GB8907700D0 (en) | 1989-04-05 | 1989-04-05 | Preparation of substituted ethenes |
GB89077002 | 1989-04-05 | ||
GB8907700.2 | 1989-04-05 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR900016119A true KR900016119A (ko) | 1990-11-12 |
KR0147820B1 KR0147820B1 (ko) | 1998-08-17 |
Family
ID=10654520
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019910700948A KR920701140A (ko) | 1989-04-05 | 1990-04-04 | 치환 에텐의 제조방법 |
KR1019900004645A KR0147820B1 (ko) | 1989-04-05 | 1990-04-04 | 치환 에텐류의 제조방법 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019910700948A KR920701140A (ko) | 1989-04-05 | 1990-04-04 | 치환 에텐의 제조방법 |
Country Status (25)
Country | Link |
---|---|
US (2) | US5371247A (ko) |
EP (1) | EP0466733B1 (ko) |
JP (2) | JP3003946B2 (ko) |
KR (2) | KR920701140A (ko) |
AT (2) | AT400030B (ko) |
BE (1) | BE1003124A5 (ko) |
CA (2) | CA2013841C (ko) |
CH (1) | CH681008A5 (ko) |
DE (2) | DE69011677T2 (ko) |
DK (2) | DK0466733T3 (ko) |
ES (2) | ES2057549T3 (ko) |
FI (2) | FI110939B (ko) |
FR (1) | FR2645535B1 (ko) |
GB (2) | GB8907700D0 (ko) |
GR (1) | GR1001302B (ko) |
HU (3) | HU9203905D0 (ko) |
IE (2) | IE61894B1 (ko) |
IL (1) | IL94002A (ko) |
IN (3) | IN170319B (ko) |
IT (1) | IT1242481B (ko) |
NL (1) | NL194699C (ko) |
PT (1) | PT93659B (ko) |
SE (1) | SE509459C2 (ko) |
WO (1) | WO1990012002A1 (ko) |
ZA (1) | ZA902592B (ko) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8907700D0 (en) * | 1989-04-05 | 1989-05-17 | Fine Organics Ltd | Preparation of substituted ethenes |
PT101031B (pt) * | 1991-11-05 | 2002-07-31 | Transkaryotic Therapies Inc | Processo para o fornecimento de proteinas por terapia genetica |
US5686588A (en) * | 1995-08-16 | 1997-11-11 | Yoo; Seo Hong | Amine acid salt compounds and process for the production thereof |
AU2001264174A1 (en) | 2000-04-21 | 2001-11-07 | Ioannis Pallikaris | Device for the shaping of a substance on the surface of a cornea |
CN104119257B (zh) * | 2013-04-26 | 2016-08-03 | 石家庄康坦福化工科技有限公司 | 一种1-甲胺基-1-甲硫基-2-硝基乙烯的制备方法 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1554153A (en) * | 1975-05-15 | 1979-10-17 | Smith Kline French Lab | Process for making 2-amino-2-alkylthionitroethylenes |
IT1168163B (it) * | 1981-08-18 | 1987-05-20 | Ausonia Farma Srl | Composto ad attivita' antiulcera, procedimento per la sua preparazione e composizioni farmaceutiche relative |
PT76557B (en) * | 1982-04-16 | 1986-01-21 | Inke Sa | Process for preparing furan derivatives and addition salts thereof and of pharmaceutical compositions containing the same |
ES8500618A1 (es) * | 1983-06-21 | 1984-11-16 | Union Quimico Farma | Procedimiento para la obtencion de n-metil-1-metiltio-2-nitroetenamina |
GB8415254D0 (en) * | 1984-06-15 | 1984-07-18 | Glaxo Group Ltd | Amine derivatives |
ES2003781A6 (es) * | 1987-02-06 | 1988-11-16 | Unio Quimico Farmaceutica S A | Procedimiento para la obtencion de n-metil-1-metiltio-2-nitroetenamina |
GB8907700D0 (en) * | 1989-04-05 | 1989-05-17 | Fine Organics Ltd | Preparation of substituted ethenes |
-
1989
- 1989-04-05 GB GB898907700A patent/GB8907700D0/en active Pending
- 1989-04-05 HU HU9203905A patent/HU9203905D0/hu unknown
-
1990
- 1990-04-04 JP JP2505189A patent/JP3003946B2/ja not_active Expired - Fee Related
- 1990-04-04 KR KR1019910700948A patent/KR920701140A/ko not_active Application Discontinuation
- 1990-04-04 WO PCT/GB1990/000501 patent/WO1990012002A1/en active IP Right Grant
- 1990-04-04 FR FR909004313A patent/FR2645535B1/fr not_active Expired - Lifetime
- 1990-04-04 AT AT0080090A patent/AT400030B/de not_active IP Right Cessation
- 1990-04-04 PT PT93659A patent/PT93659B/pt not_active IP Right Cessation
- 1990-04-04 KR KR1019900004645A patent/KR0147820B1/ko not_active IP Right Cessation
- 1990-04-04 IL IL9400290A patent/IL94002A/en not_active IP Right Cessation
- 1990-04-04 IT IT04782990A patent/IT1242481B/it active IP Right Grant
- 1990-04-04 BE BE9000381A patent/BE1003124A5/fr not_active IP Right Cessation
- 1990-04-04 EP EP90905245A patent/EP0466733B1/en not_active Expired - Lifetime
- 1990-04-04 ES ES90905245T patent/ES2057549T3/es not_active Expired - Lifetime
- 1990-04-04 DE DE69011677T patent/DE69011677T2/de not_active Expired - Fee Related
- 1990-04-04 FI FI901696A patent/FI110939B/fi active IP Right Grant
- 1990-04-04 SE SE9001236A patent/SE509459C2/sv not_active IP Right Cessation
- 1990-04-04 AT AT90905245T patent/ATE110055T1/de not_active IP Right Cessation
- 1990-04-04 NL NL9000790A patent/NL194699C/nl not_active IP Right Cessation
- 1990-04-04 DK DK90905245.8T patent/DK0466733T3/da active
- 1990-04-04 DK DK084390A patent/DK84390A/da not_active Application Discontinuation
- 1990-04-04 DE DE4010888A patent/DE4010888C2/de not_active Expired - Lifetime
- 1990-04-04 CH CH1132/90A patent/CH681008A5/fr not_active IP Right Cessation
- 1990-04-04 ZA ZA902592A patent/ZA902592B/xx unknown
- 1990-04-04 IE IE122290A patent/IE61894B1/en not_active IP Right Cessation
- 1990-04-04 IE IE122190A patent/IE65395B1/en not_active IP Right Cessation
- 1990-04-04 IN IN247/MAS/90A patent/IN170319B/en unknown
- 1990-04-04 GB GB9007568A patent/GB2230526B/en not_active Expired - Lifetime
- 1990-04-04 CA CA002013841A patent/CA2013841C/en not_active Expired - Lifetime
- 1990-04-04 CA CA002046293A patent/CA2046293C/en not_active Expired - Fee Related
- 1990-04-04 US US07/730,963 patent/US5371247A/en not_active Expired - Fee Related
- 1990-04-04 US US07/503,987 patent/US5112995A/en not_active Expired - Lifetime
- 1990-04-04 HU HU902945A patent/HUT58285A/hu unknown
- 1990-04-04 GR GR900100250A patent/GR1001302B/el not_active IP Right Cessation
- 1990-04-04 HU HU902080A patent/HU207991B/hu unknown
- 1990-04-04 ES ES9000971A patent/ES2019246A6/es not_active Expired - Fee Related
- 1990-04-04 JP JP2090034A patent/JP2954270B2/ja not_active Expired - Lifetime
-
1991
- 1991-10-04 FI FI914672A patent/FI914672A0/fi not_active Application Discontinuation
- 1991-11-25 IN IN871MA1991 patent/IN173647B/en unknown
- 1991-11-25 IN IN872MA1991 patent/IN173648B/en unknown
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