ES8701736A1 - New 5-phenyl:carbamoyl thio:barbituric acid derivs. - Google Patents

New 5-phenyl:carbamoyl thio:barbituric acid derivs.

Info

Publication number
ES8701736A1
ES8701736A1 ES554023A ES554023A ES8701736A1 ES 8701736 A1 ES8701736 A1 ES 8701736A1 ES 554023 A ES554023 A ES 554023A ES 554023 A ES554023 A ES 554023A ES 8701736 A1 ES8701736 A1 ES 8701736A1
Authority
ES
Spain
Prior art keywords
phenyl
alkyl
halo
new
substd
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
Application number
ES554023A
Other languages
Spanish (es)
Other versions
ES554023A0 (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novartis AG
Original Assignee
Ciba Geigy AG
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 Ciba Geigy AG filed Critical Ciba Geigy AG
Priority to ES554023A priority Critical patent/ES8701736A1/en
Publication of ES8701736A1 publication Critical patent/ES8701736A1/en
Publication of ES554023A0 publication Critical patent/ES554023A0/en
Expired legal-status Critical Current

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  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

HUT042458 T Three methods for preparing 5-N-substd.phenylcarbamoyl-2-thiobarbitu ric acid derivs. of formula (I), their tautomers and salts are new: Ph = (II), R1 and R2 = 1-5C alkyl or OMe; R3 = phenyl (opt. substd. by 1-3 of 1-5C alkyl, halo, NO2, 1-5C haloalkyl contg. 1-5 halo or cyano (1-4C)alkyl) or pyridyl (opt. substd. by 1-3 of 1-3C alkyl, halo, NO2 or 1-5C haloalkyl as above); R4 and R5 = H, halo, 1-5C alkyl, 1-2C haloalkyl contg. 1-3 halo, 1-3C alkoxy or NO2. - One method is reaction of ester (III) with Ph-NH2 at 50-250 deg.C. (R = 1-4C alkyl or phenyl, opt. substd. by NO2).
ES554023A 1986-04-16 1986-04-16 New 5-phenyl:carbamoyl thio:barbituric acid derivs. Expired ES8701736A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
ES554023A ES8701736A1 (en) 1986-04-16 1986-04-16 New 5-phenyl:carbamoyl thio:barbituric acid derivs.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES554023A ES8701736A1 (en) 1986-04-16 1986-04-16 New 5-phenyl:carbamoyl thio:barbituric acid derivs.

Publications (2)

Publication Number Publication Date
ES8701736A1 true ES8701736A1 (en) 1986-12-01
ES554023A0 ES554023A0 (en) 1986-12-01

Family

ID=8491150

Family Applications (1)

Application Number Title Priority Date Filing Date
ES554023A Expired ES8701736A1 (en) 1986-04-16 1986-04-16 New 5-phenyl:carbamoyl thio:barbituric acid derivs.

Country Status (1)

Country Link
ES (1) ES8701736A1 (en)

Also Published As

Publication number Publication date
ES554023A0 (en) 1986-12-01

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