GB898419A - New hydrazine carboxylic acid halides and process for preparing same - Google Patents
New hydrazine carboxylic acid halides and process for preparing sameInfo
- Publication number
- GB898419A GB898419A GB1504060A GB1504060A GB898419A GB 898419 A GB898419 A GB 898419A GB 1504060 A GB1504060 A GB 1504060A GB 1504060 A GB1504060 A GB 1504060A GB 898419 A GB898419 A GB 898419A
- Authority
- GB
- United Kingdom
- Prior art keywords
- radical
- hydrazine
- substituted
- carboxylic acid
- benzal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- -1 hydrazine carboxylic acid halides Chemical class 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 2
- 229910021529 ammonia Inorganic materials 0.000 abstract 2
- 125000000649 benzylidene group Chemical group [H]C(=[*])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
- HUTYJCTVTRHPNR-UHFFFAOYSA-N n-(benzylideneamino)-n-methylcarbamoyl chloride Chemical compound ClC(=O)N(C)N=CC1=CC=CC=C1 HUTYJCTVTRHPNR-UHFFFAOYSA-N 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- AQURFXLIZXOCLU-UHFFFAOYSA-N (4-methoxyphenyl)methylhydrazine Chemical compound COC1=CC=C(CNN)C=C1 AQURFXLIZXOCLU-UHFFFAOYSA-N 0.000 abstract 1
- UGVSIXJZAZXLRT-UHFFFAOYSA-N (benzylideneamino)-methylcarbamic acid Chemical compound OC(=O)N(C)N=CC1=CC=CC=C1 UGVSIXJZAZXLRT-UHFFFAOYSA-N 0.000 abstract 1
- JURCIGFMUVQYMG-UHFFFAOYSA-N 1-(4-methoxyphenyl)-N-[(5-nitrofuran-2-yl)methylideneamino]methanamine Chemical compound [N+](=O)([O-])C1=CC=C(C=NNCC2=CC=C(C=C2)OC)O1 JURCIGFMUVQYMG-UHFFFAOYSA-N 0.000 abstract 1
- PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 abstract 1
- DOORGKNGFZOACY-UHFFFAOYSA-N 1-amino-1-methylurea Chemical compound CN(N)C(N)=O DOORGKNGFZOACY-UHFFFAOYSA-N 0.000 abstract 1
- BXRFQSNOROATLV-UHFFFAOYSA-N 4-nitrobenzaldehyde Chemical compound [O-][N+](=O)C1=CC=C(C=O)C=C1 BXRFQSNOROATLV-UHFFFAOYSA-N 0.000 abstract 1
- SXINBFXPADXIEY-UHFFFAOYSA-N 5-Nitrofurfural Chemical compound [O-][N+](=O)C1=CC=C(C=O)O1 SXINBFXPADXIEY-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical class CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- ORPSQLWILHQEDW-UHFFFAOYSA-N N-[(4-nitrophenyl)methylideneamino]cyclohexanamine Chemical compound [N+](=O)([O-])C1=CC=C(C=NNC2CCCCC2)C=C1 ORPSQLWILHQEDW-UHFFFAOYSA-N 0.000 abstract 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000001118 alkylidene group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- OWIUPIRUAQMTTK-UHFFFAOYSA-N carbazic acid Chemical class NNC(O)=O OWIUPIRUAQMTTK-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- LHQRDAIAWDPZGH-UHFFFAOYSA-N cyclohexylhydrazine Chemical compound NNC1CCCCC1 LHQRDAIAWDPZGH-UHFFFAOYSA-N 0.000 abstract 1
- 239000000645 desinfectant Substances 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003349 semicarbazides Chemical class 0.000 abstract 1
- 125000001302 tertiary amino group Chemical group 0.000 abstract 1
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/70—Nitro radicals
- C07D307/71—Nitro radicals attached in position 5
- C07D307/72—Nitro radicals attached in position 5 with hydrocarbon radicals, substituted by nitrogen-containing radicals, attached in position 2
- C07D307/74—Nitro radicals attached in position 5 with hydrocarbon radicals, substituted by nitrogen-containing radicals, attached in position 2 by hydrazino or hydrazono or such substituted radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH7265259 | 1959-04-28 | ||
| CH7463359 | 1959-06-19 | ||
| CH236060 | 1960-03-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB898419A true GB898419A (en) | 1962-06-06 |
Family
ID=27173652
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1504060A Expired GB898419A (en) | 1959-04-28 | 1960-04-28 | New hydrazine carboxylic acid halides and process for preparing same |
Country Status (3)
| Country | Link |
|---|---|
| BE (1) | BE590177A (enrdf_load_stackoverflow) |
| ES (1) | ES257093A1 (enrdf_load_stackoverflow) |
| GB (1) | GB898419A (enrdf_load_stackoverflow) |
-
0
- BE BE590177D patent/BE590177A/xx unknown
-
1960
- 1960-04-04 ES ES0257093A patent/ES257093A1/es not_active Expired
- 1960-04-28 GB GB1504060A patent/GB898419A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE590177A (enrdf_load_stackoverflow) | |
| ES257093A1 (es) | 1960-12-01 |
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