ES430966A1 - Procedure for preparing furopirrol derivatives. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for preparing furopirrol derivatives. (Machine-translation by Google Translate, not legally binding)

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Publication number
ES430966A1
ES430966A1 ES430966A ES430966A ES430966A1 ES 430966 A1 ES430966 A1 ES 430966A1 ES 430966 A ES430966 A ES 430966A ES 430966 A ES430966 A ES 430966A ES 430966 A1 ES430966 A1 ES 430966A1
Authority
ES
Spain
Prior art keywords
radical
phenyl
optionally substituted
carbon atoms
atom
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
ES430966A
Other languages
Spanish (es)
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.)
Zeneca Inc
Original Assignee
ICI Americas Inc
ICI United States Inc
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 ICI Americas Inc, ICI United States Inc filed Critical ICI Americas Inc
Priority to ES430966A priority Critical patent/ES430966A1/en
Publication of ES430966A1 publication Critical patent/ES430966A1/en
Expired legal-status Critical Current

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Abstract

Procedure for preparing furopyrrole derivatives, of general formula: **(See formula)** wherein R1 is a hydrogen atom, an alkyl radical of 1 to 3 carbon atoms, an isobutyl or t-butyl radical, a cycloalkyl radical of 4 to 8 carbon atoms, an alkenyl radical, in which the double bond is separated from the nitrogen atom of the ring by at least one carbon atom, from 3 to 4 carbon atoms, a phenyl radical, a phenyl-alkyl radical from 8 to 10 carbon atoms optionally substituted on the phenyl ring by an atom halogen; an alkanoyl radical of 2 to 4 carbon atoms; a benzoyl radical optionally substituted by one or two halogen atoms or methyl radicals or by a methoxy radical; a phenylalkanoyl radical of 8 to 10 carbon atoms optionally substituted on the phenyl ring by a halogen atom; a pyridylcarbonyl radical or a thienylcarbonyl radical and, when R1 is hydrogen or an optionally substituted alkyl, cycloalkyl, alkenyl, phenyl or phenylalkyl radical, the pharmaceutically acceptable acid addition salts thereof; characterized in that it comprises: (a) for a compound in which R1 is a hydrogen atom or an optionally substituted alkyl, cycloalkyl, alkenyl, phenyl or phenyl radical, the reaction of a compound of formula: **(See formula)** wherein X and Y, which may be the same or different, are displaceable halogen atoms or arene sulphonyloxy or alkanesulfonyloxy radicals, with a compound of formula R2-NH2 wherein R2 is a hydrogen atom or an alkyl radical of 1 to 3 atoms carbon, an isobutyl radical, t-butyl, cycloalkyl of 4 to 8 carbon atoms, alkenyl in which the double bond is separated from the nitrogen atom by at least one carbon atom, from 3 to 4 carbon atoms, phenyl or phenyl-alkyl of 8 to 10 carbon atoms optionally substituted on the phenyl ring by a halogen atom; (b) for the compound in which R1 is hydrogen, the hydrogen replacement of the radical R3 in a compound of formula: **(See formula)** wherein R3 is an alkyl radical or an α-arylalkyl radical; (o) pazet a compound in which R1 is an alkanoyl, optionally substituted benzoyl, optionally substituted phenylalkanoyl, pyridylcarbonyl or thienylcarbonyl radical, the reaction of a compound of formula: **(See formula)** with an acid, or an acid-derived acylating agent, of the formula R4CO.OH wherein R4 is an alkyl radical of 3 or 4 carbon atoms, a phenyl radical optionally substituted by one or two halogen atoms, or methyl radicals, or by a methoxy radical, a 9 or 10 carbon atom phenylalkyl radical optionally substituted on the phenyl ring by a halogen atom, a pyridyl radical or a thienyl radical. (Machine-translation by Google Translate, not legally binding)
ES430966A 1974-10-14 1974-10-14 Procedure for preparing furopirrol derivatives. (Machine-translation by Google Translate, not legally binding) Expired ES430966A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
ES430966A ES430966A1 (en) 1974-10-14 1974-10-14 Procedure for preparing furopirrol derivatives. (Machine-translation by Google Translate, not legally binding)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES430966A ES430966A1 (en) 1974-10-14 1974-10-14 Procedure for preparing furopirrol derivatives. (Machine-translation by Google Translate, not legally binding)

Publications (1)

Publication Number Publication Date
ES430966A1 true ES430966A1 (en) 1977-01-16

Family

ID=8467740

Family Applications (1)

Application Number Title Priority Date Filing Date
ES430966A Expired ES430966A1 (en) 1974-10-14 1974-10-14 Procedure for preparing furopirrol derivatives. (Machine-translation by Google Translate, not legally binding)

Country Status (1)

Country Link
ES (1) ES430966A1 (en)

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