ES419142A1 - 2-2-2-methyl-5-nitro-1-imidazolyl-ethyl-2-thiopseudoureas and related compounds - Google Patents
2-2-2-methyl-5-nitro-1-imidazolyl-ethyl-2-thiopseudoureas and related compoundsInfo
- Publication number
- ES419142A1 ES419142A1 ES419142A ES419142A ES419142A1 ES 419142 A1 ES419142 A1 ES 419142A1 ES 419142 A ES419142 A ES 419142A ES 419142 A ES419142 A ES 419142A ES 419142 A1 ES419142 A1 ES 419142A1
- Authority
- ES
- Spain
- Prior art keywords
- formula
- hydrogen
- ch2ch2x
- radical
- general formula
- 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
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- JTLNYEGYOSBRDX-UHFFFAOYSA-N 1-nitroethyne Chemical group [O-][N+](=O)C#C JTLNYEGYOSBRDX-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000005948 methanesulfonyloxy group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 231100000252 nontoxic Toxicity 0.000 abstract 1
- 230000003000 nontoxic effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 abstract 1
- -1 vinylene, nitrovinylene Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/91—Nitro radicals
- C07D233/92—Nitro radicals attached in position 4 or 5
- C07D233/94—Nitro radicals attached in position 4 or 5 with hydrocarbon radicals, substituted by oxygen or sulfur atoms, attached to other ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/84—Sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Procedure for preparing thioseudourea derivatives, of general formula: **(See formula)** or a pharmaceutically acceptable, non-toxic acid addition salt thereof, in which formula R is hydrogen or an alkyl radical of 1 to 7 carbon atoms, R1 and R'' are each hydrogen or an alkyl radical of 1 at 7 carbon atoms, or R'and R''are combined to form a vinylene, nitrovinylene or trimethylene grouping; characterized by comprising: reacting a compound of the general formula: **(See formula)** where A is hydrogen or a radical of formula -CH2CH2X, where X is halogen, toluenesulfonyloxy or methanesulfonyloxy; with a compound of general formula: **(See formula)** where Z is hydrogen when A is -CH2CH2X; Z is a radical of formula -CH2CH2X when A is hydrogen; and R, R'and R''are defined as above, with the proviso that R' and R'' may combine to form a nitrovinylene grouping only when Z is -CH2CH2X. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US29306972A | 1972-09-28 | 1972-09-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES419142A1 true ES419142A1 (en) | 1976-07-16 |
Family
ID=23127520
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES419142A Expired ES419142A1 (en) | 1972-09-28 | 1973-09-27 | 2-2-2-methyl-5-nitro-1-imidazolyl-ethyl-2-thiopseudoureas and related compounds |
Country Status (10)
| Country | Link |
|---|---|
| JP (1) | JPS4970967A (en) |
| AR (1) | AR197529A1 (en) |
| AU (1) | AU473626B2 (en) |
| BE (1) | BE805432A (en) |
| CA (1) | CA967961A (en) |
| DE (1) | DE2348525A1 (en) |
| ES (1) | ES419142A1 (en) |
| FR (1) | FR2201094B1 (en) |
| GB (1) | GB1393228A (en) |
| ZA (1) | ZA737629B (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1542840A (en) * | 1975-02-03 | 1979-03-28 | Smith Kline French Lab | Heterocyclic dithiocarbamates and isothioureas |
| USRE34201E (en) * | 1989-04-20 | 1993-03-23 | Anaquest, Inc. | N-aryl-N-[4-(1-heterocyclicalkyl)piperidinyl]amides and pharmaceutical compositions and methods employing such compounds |
| JPH0717971A (en) * | 1993-07-02 | 1995-01-20 | Takeda Chem Ind Ltd | Imidazole derivative, production and use thereof |
| KR20210146318A (en) | 2019-03-29 | 2021-12-03 | 유니베르시떼 드 파리 | Imidazoline derivatives as CXCR4 modulators |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1277666A (en) * | 1969-12-17 | 1972-06-14 | Pfizer Ltd | Improvements in the n-alkylation of nitroimidazoles |
-
1973
- 1973-09-27 DE DE19732348525 patent/DE2348525A1/en active Pending
- 1973-09-27 ZA ZA737629*A patent/ZA737629B/en unknown
- 1973-09-27 AR AR250267A patent/AR197529A1/en active
- 1973-09-27 CA CA182,043A patent/CA967961A/en not_active Expired
- 1973-09-27 AU AU60814/73A patent/AU473626B2/en not_active Expired
- 1973-09-27 GB GB4522473A patent/GB1393228A/en not_active Expired
- 1973-09-27 ES ES419142A patent/ES419142A1/en not_active Expired
- 1973-09-28 FR FR7334906A patent/FR2201094B1/fr not_active Expired
- 1973-09-28 BE BE136139A patent/BE805432A/en unknown
- 1973-09-28 JP JP48110107A patent/JPS4970967A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| AU473626B2 (en) | 1976-06-24 |
| BE805432A (en) | 1974-03-28 |
| AR197529A1 (en) | 1974-04-15 |
| JPS4970967A (en) | 1974-07-09 |
| GB1393228A (en) | 1975-05-07 |
| DE2348525A1 (en) | 1974-04-11 |
| CA967961A (en) | 1975-05-20 |
| FR2201094B1 (en) | 1977-01-28 |
| ZA737629B (en) | 1974-12-24 |
| AU6081473A (en) | 1975-03-27 |
| FR2201094A1 (en) | 1974-04-26 |
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