SU517587A1 - Способ получени производных 2оксфенилмочевины - Google Patents

Способ получени производных 2оксфенилмочевины

Info

Publication number
SU517587A1
SU517587A1 SU1823300A SU1823300A SU517587A1 SU 517587 A1 SU517587 A1 SU 517587A1 SU 1823300 A SU1823300 A SU 1823300A SU 1823300 A SU1823300 A SU 1823300A SU 517587 A1 SU517587 A1 SU 517587A1
Authority
SU
USSR - Soviet Union
Prior art keywords
preparing
derivatives
oxphenylurea
product
benzyl
Prior art date
Application number
SU1823300A
Other languages
English (en)
Inventor
Михайлов Шиндаров Любомир
Симеонов Галабов Ангел
Симов Антонов Димитар
Атанасова Нейкова Надежда
Атанасов Давидков Крум
Димитрова Васильева Веселина
Борисова Калчева Венета
Станева Стойчева Душка
Original Assignee
Медицинска Академие (Инопредприятие)
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Медицинска Академие (Инопредприятие) filed Critical Медицинска Академие (Инопредприятие)
Application granted granted Critical
Publication of SU517587A1 publication Critical patent/SU517587A1/ru

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C335/04—Derivatives of thiourea
    • C07C335/16—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C335/18—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C275/32—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
    • C07C275/34—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms having nitrogen atoms of urea groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring

Description

растворе и температура плавлени  очищенного .продукта составл ет 137-138° С.
Найдено, %: С 58,55; Н 4,66; N 9,43.
CisHisCINaSO.
Вычислено, %: С 58,82; Н 4,90; N 9,15.
Аналогично полученные вещества прюведены в та-бл. 1.
Пример 2. N-Бeнзил-N-(2-o.кcифeнил)N-п .ропилмоч евина.
2,0 г N-бензилбензаксазолона и 10,0 м.л 50%-HOiro водного раствора пролиламина кип т т совместно в течение 7 ч. После охлаждени  реакционную смесь нейтрализуют и образовающийс  осадок отфильтровывают. После растворени  его в 10%:-ном растворе гидрата окиси натри  продукт осаждают разбавленной сол ной кислотой, причем очищенный та.ким способом продукт имеет вес 1,85 г (72% от теоретического). Затем продукт перекристаллизовывают из спиртового раствора . Температура его плавлени  составл ет 135-136° С.
Найдено, %: С 71,82; N 9,71; Н 7,15.
Ci7H2oN202.
Вычислено, %: С 71,83; N 9,85; Н 7,04.
Таблица I
Таблица 2
Ф О р м ула изобретени 
Способ получени  производных 2-оксифенил .мочевины общей формулы I
ОН
N(Ri)C(H3)NHEj GI - С4-ал.кил или бензил; - С - С4-ал«ил, бензил или циклогекКз - кислород или сера; Х--водород, хлор или сульфонамидна  15 группа; Y - водород или бром.
Продолжение табл. 2
отличающийс  тем, что соединение общей формулы II
(П), где RI, Кз, X и Y имеют указанные выше значени , подвергают взаимодействию с избытком амина общей формулы III где RS имеет указанные выще значени , при 60-100° С.
SU1823300A 1971-08-23 1972-08-22 Способ получени производных 2оксфенилмочевины SU517587A1 (ru)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
BG1722371 1971-08-23

Publications (1)

Publication Number Publication Date
SU517587A1 true SU517587A1 (ru) 1976-06-15

Family

ID=3897721

Family Applications (1)

Application Number Title Priority Date Filing Date
SU1823300A SU517587A1 (ru) 1971-08-23 1972-08-22 Способ получени производных 2оксфенилмочевины

Country Status (7)

Country Link
US (1) US3846491A (ru)
JP (1) JPS5734259B2 (ru)
CH (1) CH574401A5 (ru)
DE (1) DE2241471C3 (ru)
FR (1) FR2150833B1 (ru)
GB (1) GB1350710A (ru)
SU (1) SU517587A1 (ru)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2303761A1 (de) * 1973-01-26 1974-08-01 Henkel & Cie Gmbh Neue n,n'-disubstituierte thioharnstoffe, deren herstellung sowie verwendung als antimikrobielle substanzen
JPS62137067U (ru) * 1986-02-24 1987-08-28
IL102548A (en) * 1991-08-02 1998-08-16 Medivir Ab Use of painting derivatives in the preparation of drugs for VIH inhibition and treatment of SDIA and new compounds
US5593993A (en) * 1991-08-02 1997-01-14 Medivir Ab Method for inhibition of HIV related viruses
JPH06182010A (ja) * 1992-06-19 1994-07-05 Mizuno Corp Ｆｒｐ製バット
CA2197364A1 (en) * 1996-02-15 1997-08-16 Toshikazu Suzuki Phenol compound and process for preparing the same
US9540322B2 (en) 2008-08-18 2017-01-10 Yale University MIF modulators
US9643922B2 (en) * 2008-08-18 2017-05-09 Yale University MIF modulators
WO2010021693A2 (en) * 2008-08-18 2010-02-25 Yale University Mif modulators

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2795610A (en) * 1955-03-31 1957-06-11 Du Pont Hydroxy-phenyl alkyl ureas

Also Published As

Publication number Publication date
FR2150833B1 (ru) 1975-10-17
US3846491A (en) 1974-11-05
JPS4832843A (ru) 1973-05-02
DE2241471C3 (de) 1981-10-01
GB1350710A (en) 1974-04-24
CH574401A5 (ru) 1976-04-15
FR2150833A1 (ru) 1973-04-13
JPS5734259B2 (ru) 1982-07-22
DE2241471B2 (de) 1980-11-06
DE2241471A1 (de) 1973-03-22

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