GB920412A - Pyrimidine derivatives and the manufacture thereof - Google Patents
Pyrimidine derivatives and the manufacture thereofInfo
- Publication number
- GB920412A GB920412A GB12355/58A GB1235558A GB920412A GB 920412 A GB920412 A GB 920412A GB 12355/58 A GB12355/58 A GB 12355/58A GB 1235558 A GB1235558 A GB 1235558A GB 920412 A GB920412 A GB 920412A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methoxy
- hydrogen
- compounds
- formula
- carbon atoms
- 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
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16C—SHAFTS; FLEXIBLE SHAFTS; ELEMENTS OR CRANKSHAFT MECHANISMS; ROTARY BODIES OTHER THAN GEARING ELEMENTS; BEARINGS
- F16C3/00—Shafts; Axles; Cranks; Eccentrics
- F16C3/04—Crankshafts, eccentric-shafts; Cranks, eccentrics
- F16C3/06—Crankshafts
- F16C3/14—Features relating to lubrication
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
- A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Mechanical Engineering (AREA)
- Ocean & Marine Engineering (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
The invention comprises compounds of the formula <FORM:0920412/IV(a)/1> wherein R1 is an alkyl group of 1-4 carbon atoms, R2 is hydrogen, isopropyl, an alkyl group of 4-6 carbon atoms or benzyl and R3, R4 and R5 are hydrogen or halogen e.g. bromine; when at least one of R3, R4 and R5 is halogen R2 may also be n-propyl. The compounds are prepared by formylating a compound of the formula <FORM:0920412/IV(a)/2> wherein R6 has the values of R2 other than hydrogen and R7 is an alkyl group of 1-4 carbon atoms, condensing the product with guanidine to give a 2-amino-4-hydroxy-5benzyl-pyrimidine derivative, chlorinating e.g. with POCl3 and aminating. Compounds wherein R2 is hydrogen are made by hydrogenolysis of a compound wherein R2 is a benzyl group. Compounds wherein one or more of R3, R4 and R5 are halogen atoms may be prepared by halogenating, e.g. brominating, the corresponding unsubstituted compound. Hydrocinnamic esters of the formula II used as starting materials namely 3-methoxy-4isopropoxy-, 3-methoxy-4-butoxy-, 3-methoxy4-isoamyloxy-, 3-methoxy-4-propoxy-5-bromoand 3 - methoxy - 4 - butoxy-5-bromo-, hydrocinnamic acid ethyl esters are made by alkylating vanillin, or the appropriately substituted vanillin, in the 4-position, condensing the 3methoxy-4-alkoxy-benzaldehyde (or bromobenzaldehyde) obtained with malonic acid, esterifying the resulting corresponding substituted cinnamic acid to give the ethyl ester and reducing catalytically. Specifications 598,514, 671,926, 671,927 and 734,801 are referred to.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB12355/58A GB920412A (en) | 1958-04-18 | 1958-04-18 | Pyrimidine derivatives and the manufacture thereof |
CH121368A CH457451A (en) | 1958-04-18 | 1959-04-17 | Process for the preparation of pyrimidine derivatives |
CH7217059A CH451944A (en) | 1958-04-18 | 1959-04-17 | Process for the preparation of pyrimidine derivatives |
BE577871A BE577871A (en) | 1958-04-18 | 1959-04-18 | Pyrimidine derivatives and their preparation |
FR837267A FR495M (en) | 1958-04-18 | 1960-08-30 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB12355/58A GB920412A (en) | 1958-04-18 | 1958-04-18 | Pyrimidine derivatives and the manufacture thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
GB920412A true GB920412A (en) | 1963-03-06 |
Family
ID=10002999
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12355/58A Expired GB920412A (en) | 1958-04-18 | 1958-04-18 | Pyrimidine derivatives and the manufacture thereof |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE577871A (en) |
CH (2) | CH457451A (en) |
FR (1) | FR495M (en) |
GB (1) | GB920412A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2249532A1 (en) * | 1971-10-12 | 1973-04-26 | Wellcome Found | PROCESS FOR THE PREPARATION OF 2,4-DIAMINO-5-BENZYLPYRIMIDINES |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3603577A1 (en) * | 1986-02-06 | 1987-08-13 | Joachim K Prof Dr Seydel | NEW SUBSTITUTED 2,4-DIAMINO-5-BENZYLPYRIMIDINE, THEIR PRODUCTION AND USE THEREOF AS A MEDICINE WITH ANTIBACTERIAL EFFECTIVENESS |
-
1958
- 1958-04-18 GB GB12355/58A patent/GB920412A/en not_active Expired
-
1959
- 1959-04-17 CH CH121368A patent/CH457451A/en unknown
- 1959-04-17 CH CH7217059A patent/CH451944A/en unknown
- 1959-04-18 BE BE577871A patent/BE577871A/en unknown
-
1960
- 1960-08-30 FR FR837267A patent/FR495M/fr active Active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2249532A1 (en) * | 1971-10-12 | 1973-04-26 | Wellcome Found | PROCESS FOR THE PREPARATION OF 2,4-DIAMINO-5-BENZYLPYRIMIDINES |
Also Published As
Publication number | Publication date |
---|---|
FR495M (en) | 1961-05-08 |
CH457451A (en) | 1968-06-15 |
BE577871A (en) | 1959-08-17 |
CH451944A (en) | 1968-05-15 |
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