KR100842793B1 - N-메틸-n'-니트로구아니딘의 제조방법 - Google Patents
N-메틸-n'-니트로구아니딘의 제조방법 Download PDFInfo
- Publication number
- KR100842793B1 KR100842793B1 KR1020027008254A KR20027008254A KR100842793B1 KR 100842793 B1 KR100842793 B1 KR 100842793B1 KR 1020027008254 A KR1020027008254 A KR 1020027008254A KR 20027008254 A KR20027008254 A KR 20027008254A KR 100842793 B1 KR100842793 B1 KR 100842793B1
- Authority
- KR
- South Korea
- Prior art keywords
- nitroguanidine
- methyl
- formula
- range
- reaction temperature
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 5
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 claims abstract description 15
- XCXKNNGWSDYMMS-UHFFFAOYSA-N 2-methyl-1-nitroguanidine Chemical compound CNC(N)=N[N+]([O-])=O XCXKNNGWSDYMMS-UHFFFAOYSA-N 0.000 claims abstract description 10
- IDCPFAYURAQKDZ-UHFFFAOYSA-N 1-nitroguanidine Chemical compound NC(=N)N[N+]([O-])=O IDCPFAYURAQKDZ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 150000007522 mineralic acids Chemical class 0.000 claims abstract description 4
- 150000007524 organic acids Chemical class 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 22
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 239000007864 aqueous solution Substances 0.000 abstract 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- BJRRHBMKDXBQBE-UHFFFAOYSA-N 1-methyl-1-nitroguanidine Chemical compound NC(=N)N(C)[N+]([O-])=O BJRRHBMKDXBQBE-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical group SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- NQMRYBIKMRVZLB-UHFFFAOYSA-N methylamine hydrochloride Chemical compound [Cl-].[NH3+]C NQMRYBIKMRVZLB-UHFFFAOYSA-N 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- -1 methylmercapto group Chemical group 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000007039 two-step reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C277/00—Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C277/00—Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
- C07C277/08—Preparation of guanidine or its derivatives, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups of substituted guanidines
Abstract
Description
Claims (8)
- 제1항에 있어서, 반응 온도가 0 내지 40℃ 범위임을 특징으로 하는 방법.
- 제1항에 있어서, 반응 온도가 10 내지 30℃ 범위임을 특징으로 하는 방법.
- 제1항에 있어서, 반응 온도가 20 내지 30℃ 범위임을 특징으로 하는 방법.
- 제1항에 있어서, pH가 11 내지 13 범위임을 특징으로 하는 방법.
- 제1항에 있어서, pH가 11.5 내지 13 범위임을 특징으로 하는 방법.
- 제6항에 있어서, 반응 온도가 0 내지 40℃ 범위임을 특징으로 하는 방법.
- 제6항에 있어서, 반응 온도가 20 내지 40℃ 범위임을 특징으로 하는 방법.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10000891A DE10000891A1 (de) | 2000-01-12 | 2000-01-12 | Verfahren zur Herstellung von N-Methyl-N'-nitroguanidin |
DE10000891.7 | 2000-01-12 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20020067575A KR20020067575A (ko) | 2002-08-22 |
KR100842793B1 true KR100842793B1 (ko) | 2008-07-01 |
Family
ID=7627225
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020027008254A KR100842793B1 (ko) | 2000-01-12 | 2001-01-03 | N-메틸-n'-니트로구아니딘의 제조방법 |
Country Status (9)
Country | Link |
---|---|
US (1) | US6720451B2 (ko) |
EP (1) | EP1268411B1 (ko) |
JP (1) | JP4700880B2 (ko) |
KR (1) | KR100842793B1 (ko) |
AT (1) | ATE381536T1 (ko) |
AU (1) | AU2001223714A1 (ko) |
DE (2) | DE10000891A1 (ko) |
TW (1) | TWI291947B (ko) |
WO (1) | WO2001051458A1 (ko) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10003834A1 (de) * | 2000-01-28 | 2001-08-02 | Nigu Chemie Gmbh | Verfahren zur Herstellung von 1-Methyl-3-nitroguanidin |
CN101565392A (zh) * | 2008-04-21 | 2009-10-28 | 南通天泽化工有限公司 | 一种甲基硝基胍及其制备方法 |
CN103641746B (zh) * | 2013-11-22 | 2016-03-30 | 青岛文创科技有限公司 | 一种n-甲基-n’硝基胍的合成工艺 |
CN103787922B (zh) * | 2014-03-04 | 2016-06-01 | 新昌县鸿吉电子科技有限公司 | 一种合成硝基取代化合物的工业催化方法 |
CN106986790A (zh) * | 2017-05-25 | 2017-07-28 | 宁夏贝利特生物科技有限公司 | 用生产硝基胍后的稀硫酸生产n‑甲基‑n′‑硝基胍的方法 |
CN107382789A (zh) * | 2017-06-29 | 2017-11-24 | 南通天泽化工有限公司 | 一种甲基硝基胍的制备方法 |
CN107698466A (zh) * | 2017-11-09 | 2018-02-16 | 宁夏贝利特生物科技有限公司 | 一种n‑甲基‑n′‑硝基胍的制备方法 |
CN109053498A (zh) * | 2018-09-27 | 2018-12-21 | 南通天泽化工有限公司 | 一种1-甲基-1,2-二硝基胍的制备方法 |
CN110128300A (zh) * | 2019-05-10 | 2019-08-16 | 宁夏贝利特生物科技有限公司 | 一种制备1-甲基-3-硝基胍的方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09255651A (ja) * | 1996-03-25 | 1997-09-30 | Bayer Ag | N−メチル−n′−ニトログアニジンの製造法 |
JP2007009902A (ja) * | 2005-06-30 | 2007-01-18 | Hyundai Motor Co Ltd | Lpiエンジンの燃料供給システム |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19712885A1 (de) * | 1997-03-27 | 1998-10-01 | Bayer Ag | Verfahren zur Herstellung von N-Alkyl-N'-nitroguanidinen |
US6118007A (en) * | 1997-03-31 | 2000-09-12 | Mitsui Chemicals, Inc. | Preparation process of nitroguanidine derivatives |
EP1133468B1 (de) * | 1998-11-25 | 2003-08-20 | Dynamit Nobel GmbH Explosivstoff- und Systemtechnik | Verfahren zur herstellung von n-alkyl-n'-nitroguanidin |
DE10003834A1 (de) * | 2000-01-28 | 2001-08-02 | Nigu Chemie Gmbh | Verfahren zur Herstellung von 1-Methyl-3-nitroguanidin |
-
2000
- 2000-01-12 DE DE10000891A patent/DE10000891A1/de not_active Withdrawn
-
2001
- 2001-01-03 WO PCT/EP2001/000015 patent/WO2001051458A1/de active IP Right Grant
- 2001-01-03 JP JP2001551840A patent/JP4700880B2/ja not_active Expired - Fee Related
- 2001-01-03 DE DE50113398T patent/DE50113398D1/de not_active Expired - Lifetime
- 2001-01-03 EP EP01900112A patent/EP1268411B1/de not_active Expired - Lifetime
- 2001-01-03 AU AU2001223714A patent/AU2001223714A1/en not_active Abandoned
- 2001-01-03 KR KR1020027008254A patent/KR100842793B1/ko active IP Right Grant
- 2001-01-03 AT AT01900112T patent/ATE381536T1/de active
- 2001-01-03 US US10/169,842 patent/US6720451B2/en not_active Expired - Lifetime
- 2001-01-11 TW TW090100573A patent/TWI291947B/zh not_active IP Right Cessation
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09255651A (ja) * | 1996-03-25 | 1997-09-30 | Bayer Ag | N−メチル−n′−ニトログアニジンの製造法 |
JP2007009902A (ja) * | 2005-06-30 | 2007-01-18 | Hyundai Motor Co Ltd | Lpiエンジンの燃料供給システム |
Non-Patent Citations (1)
Title |
---|
한국공개특허공보 제1999-022251호* |
Also Published As
Publication number | Publication date |
---|---|
WO2001051458A1 (de) | 2001-07-19 |
EP1268411A1 (de) | 2003-01-02 |
AU2001223714A1 (en) | 2001-07-24 |
EP1268411B1 (de) | 2007-12-19 |
TWI291947B (en) | 2008-01-01 |
JP2003519677A (ja) | 2003-06-24 |
KR20020067575A (ko) | 2002-08-22 |
ATE381536T1 (de) | 2008-01-15 |
US20030004376A1 (en) | 2003-01-02 |
JP4700880B2 (ja) | 2011-06-15 |
US6720451B2 (en) | 2004-04-13 |
DE50113398D1 (de) | 2008-01-31 |
DE10000891A1 (de) | 2001-07-19 |
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