NO118850B - - Google Patents
Download PDFInfo
- Publication number
- NO118850B NO118850B NO161322A NO16132266A NO118850B NO 118850 B NO118850 B NO 118850B NO 161322 A NO161322 A NO 161322A NO 16132266 A NO16132266 A NO 16132266A NO 118850 B NO118850 B NO 118850B
- Authority
- NO
- Norway
- Prior art keywords
- oxo
- tetrahydro
- thiazolyl
- imidazole
- unsubstituted
- Prior art date
Links
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical class O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 4
- 238000010992 reflux Methods 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000007858 starting material Substances 0.000 description 4
- 235000011121 sodium hydroxide Nutrition 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- BCMYXYHEMGPZJN-UHFFFAOYSA-N 1-chloro-2-isocyanatoethane Chemical compound ClCCN=C=O BCMYXYHEMGPZJN-UHFFFAOYSA-N 0.000 description 1
- RBQJOSROXTWQOK-UHFFFAOYSA-N 1-nitroimidazolidin-2-one Chemical class [O-][N+](=O)N1CCNC1=O RBQJOSROXTWQOK-UHFFFAOYSA-N 0.000 description 1
- WZELXJBMMZFDDU-UHFFFAOYSA-N Imidazol-2-one Chemical class O=C1N=CC=N1 WZELXJBMMZFDDU-UHFFFAOYSA-N 0.000 description 1
- 241000534944 Thia Species 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002141 anti-parasite Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- -1 haloethyl isocyanate Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000000802 nitrating effect Effects 0.000 description 1
- 238000006396 nitration reaction Methods 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
Landscapes
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Temperature-Responsive Valves (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH76665A CH462830A (de) | 1965-01-20 | 1965-01-20 | Verfahren zur Herstellung von 1-(5-Nitrothiazolyl-(2))-2-oxo-tetrahydroimidazolen |
| CH842065A CH485768A (de) | 1965-01-20 | 1965-06-16 | Verfahren zur Herstellung von 3-Nitro-1-(5-nitrothiazolyl(2))-2-oxo-tetrahydro-imidazolen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO118850B true NO118850B (de) | 1970-02-23 |
Family
ID=25685615
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO161323A NO119534B (de) | 1965-01-20 | 1966-01-19 | |
| NO161322A NO118850B (de) | 1965-01-20 | 1966-01-19 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO161323A NO119534B (de) | 1965-01-20 | 1966-01-19 |
Country Status (15)
| Country | Link |
|---|---|
| US (2) | US3385861A (de) |
| AT (1) | AT255412B (de) |
| BE (2) | BE675321A (de) |
| BR (2) | BR6676544D0 (de) |
| CH (2) | CH462830A (de) |
| DE (2) | DE1670325C3 (de) |
| DK (2) | DK120395B (de) |
| ES (1) | ES321947A2 (de) |
| FI (1) | FI46379B (de) |
| FR (3) | FR1463612A (de) |
| GB (2) | GB1127862A (de) |
| NL (2) | NL6600708A (de) |
| NO (2) | NO119534B (de) |
| OA (1) | OA01895A (de) |
| SE (2) | SE311908B (de) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3515538A (en) * | 1965-08-11 | 1970-06-02 | Mitsui Koatsu Chem Inc | 2-acylamino-4-methyl-5-halothiazoles as selective herbicides |
| US3475446A (en) * | 1967-06-27 | 1969-10-28 | Parke Davis & Co | N-(5-nitro-2-thiazolyl)-cycloalkanecarboxamides |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE632989A (de) * | 1962-05-30 | |||
| NL6410031A (de) * | 1962-05-30 | 1965-03-01 |
-
1965
- 1965-01-20 CH CH76665A patent/CH462830A/de unknown
- 1965-06-16 CH CH842065A patent/CH485768A/de not_active IP Right Cessation
- 1965-12-28 US US517069A patent/US3385861A/en not_active Expired - Lifetime
-
1966
- 1966-01-03 US US517986A patent/US3391153A/en not_active Expired - Lifetime
- 1966-01-04 GB GB331/66A patent/GB1127862A/en not_active Expired
- 1966-01-04 GB GB330/66A patent/GB1127861A/en not_active Expired
- 1966-01-08 DE DE1670325A patent/DE1670325C3/de not_active Expired
- 1966-01-08 DE DE19661670326 patent/DE1670326A1/de active Pending
- 1966-01-14 FR FR45903A patent/FR1463612A/fr not_active Expired
- 1966-01-18 FI FI0123/66A patent/FI46379B/fi active
- 1966-01-18 OA OA52326A patent/OA01895A/xx unknown
- 1966-01-18 FR FR46271A patent/FR1463725A/fr not_active Expired
- 1966-01-19 BE BE675321D patent/BE675321A/xx unknown
- 1966-01-19 NL NL6600708A patent/NL6600708A/xx unknown
- 1966-01-19 BE BE675322D patent/BE675322A/xx unknown
- 1966-01-19 BR BR176544/66A patent/BR6676544D0/pt unknown
- 1966-01-19 NO NO161323A patent/NO119534B/no unknown
- 1966-01-19 AT AT49366A patent/AT255412B/de active
- 1966-01-19 BR BR176541/66A patent/BR6676541D0/pt unknown
- 1966-01-19 NO NO161322A patent/NO118850B/no unknown
- 1966-01-19 SE SE687/66A patent/SE311908B/xx unknown
- 1966-01-19 SE SE688/66A patent/SE311909B/xx unknown
- 1966-01-19 DK DK28366AA patent/DK120395B/da unknown
- 1966-01-19 DK DK28466AA patent/DK122527B/da unknown
- 1966-01-19 ES ES321947A patent/ES321947A2/es not_active Expired
- 1966-01-19 NL NL6600712A patent/NL6600712A/xx unknown
- 1966-04-14 FR FR57600A patent/FR5274M/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| US3385861A (en) | 1968-05-28 |
| FR1463612A (fr) | 1966-12-23 |
| GB1127862A (en) | 1968-09-18 |
| DK120395B (da) | 1971-05-24 |
| FR5274M (de) | 1967-07-31 |
| BE675321A (de) | 1966-07-19 |
| CH462830A (de) | 1968-09-30 |
| SE311909B (de) | 1969-06-30 |
| ES321947A2 (es) | 1968-02-16 |
| DE1670326A1 (de) | 1970-11-05 |
| US3391153A (en) | 1968-07-02 |
| BR6676541D0 (pt) | 1973-09-06 |
| FR1463725A (fr) | 1966-12-23 |
| OA01895A (fr) | 1970-02-04 |
| SE311908B (de) | 1969-06-30 |
| DE1670325C3 (de) | 1975-09-04 |
| BR6676544D0 (pt) | 1973-09-06 |
| GB1127861A (en) | 1968-09-18 |
| NL6600712A (de) | 1966-07-21 |
| BE675322A (de) | 1966-07-19 |
| AT255412B (de) | 1967-07-10 |
| NO119534B (de) | 1970-06-01 |
| CH485768A (de) | 1970-02-15 |
| NL6600708A (de) | 1966-07-21 |
| DE1670325A1 (de) | 1970-10-29 |
| FI46379B (de) | 1972-11-30 |
| DK122527B (da) | 1972-03-13 |
| DE1670325B2 (de) | 1975-01-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2971985A (en) | Process for the preparation of 4, 4'-dichlorodiphenylsulfone | |
| NO143531B (no) | Fremgangsmaate for fremstilling av acylerte benzoksazolinon-derivater | |
| NO118850B (de) | ||
| JPH0143753B2 (de) | ||
| JPS5846501B2 (ja) | ジアミノナフタリンノ セイゾウホウホウ | |
| US3794636A (en) | Process for preparation of thiazole hydrohalides | |
| JPS6233164A (ja) | ２−置換ベンゾチアゾ−ルの製造方法 | |
| US1763556A (en) | Tri halogen benzene sulphochloride and process for preparing the same | |
| US3210348A (en) | 6h-6-trichloromethylmercapto-dibenzo[c, e][1, 2]thiazine 5, 5-dioxide compounds | |
| CN110845405A (zh) | 一种7-氯喹哪啶的合成方法 | |
| US2335273A (en) | 3,3-dihalogenoxindoles | |
| JPS6210510B2 (de) | ||
| US4288620A (en) | Process for the production of 4-acylamido-2-nitro-1-alkoxybenzenes | |
| US2531465A (en) | Halomethyl-4-halobenzanthrones | |
| US6114584A (en) | Method of preparing brominated substituted anilines | |
| US3931321A (en) | Process for the preparation of O-aminothiophenols | |
| US1897516A (en) | Process for manufacturing phenylthioglycollic acids, containing halogen and alkyl croups in their molecule | |
| JPH07304726A (ja) | ２−アリール−エタン−スルホン酸類の製造方法 | |
| US2439302A (en) | Preparation of benzotetronic acid | |
| IL27766A (en) | Process for the preparation of 3,4-dihydro-4-oxo-1,2,3-benzotriazinyl-3-yl methyl thionothiol-phosphoric(-phosphonic,-phosphinic)acid esters | |
| US1787315A (en) | New compounds of the thiazolic series and process of making same | |
| US3225048A (en) | Process for the preparation of 2,6-diketo-8-thiapurines | |
| JP4913589B2 (ja) | １，２−ベンズイソキサゾール−３−メタンスルホンアミドのワンポット製造法 | |
| JPS60166673A (ja) | ３−位が置換された２（３ｈ）−ベンズチアゾロンの製造方法 | |
| PL180016B1 (en) | Novel method of obtaining 3,4-dihydroxy-5-nitrobenzaldehyde |