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ES441470A1 - Obtaining procedure of 1- (2-hydroxymethyl-1-fenoxy) -2-pharmacologically active propanolamines. (Machine-translation by Google Translate, not legally binding) - Google Patents

Obtaining procedure of 1- (2-hydroxymethyl-1-fenoxy) -2-pharmacologically active propanolamines. (Machine-translation by Google Translate, not legally binding)

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Publication number
ES441470A1
ES441470A1ES441470AES441470AES441470A1ES 441470 A1ES441470 A1ES 441470A1ES 441470 AES441470 AES 441470AES 441470 AES441470 AES 441470AES 441470 A1ES441470 A1ES 441470A1
Authority
ES
Spain
Prior art keywords
hydroxymethyl
propanolamines
translation
legally binding
google translate
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
ES441470A
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.)
Especialidades Latinas Medicamentos Universales SA
Original Assignee
Especialidades Latinas Medicamentos Universales SA
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 Especialidades Latinas Medicamentos Universales SAfiledCriticalEspecialidades Latinas Medicamentos Universales SA
Priority to ES441470ApriorityCriticalpatent/ES441470A1/en
Publication of ES441470A1publicationCriticalpatent/ES441470A1/en
Expiredlegal-statusCriticalCurrent

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Abstract

Procedure for obtaining pharmacologically active 1- (2-hydroxymethyl-1-phenoxy) -2-propanolamines, which correspond to the general formula: ** (see formula) ** Wherein the radicals that are attached to the amino nitrogen are: (see graphic) Whose process is characterized in that the reaction is carried out in two stages, in the first stage the salicylic alcohol reacts with aqueous or alcoholic sodium hydroxide, producing its sodium salt, which treated with epichlorohydrin at a temperature ranging from -6º to 60º c. 18 to 22 hours. Then extract with chloroform, acidify the organic layer with acetic acid and then wash with water, until non-acidic ph, dry with anhydrous sodium sulfate or other appropriate desiccant, remove the chloroform under reduced pressure and distill the residue under vacuum, produce 1- (2-hydroxymethyl-1-phenoxy) -2,3-epoxy-propane and, because in a second step, the amine corresponding to each case is added to the glycidyl ether thus obtained, dissolved in ethanol, methanol or tetrahydrofuran. (Machine-translation by Google Translate, not legally binding)
ES441470A1975-10-031975-10-03Obtaining procedure of 1- (2-hydroxymethyl-1-fenoxy) -2-pharmacologically active propanolamines. (Machine-translation by Google Translate, not legally binding)ExpiredES441470A1 (en)

Priority Applications (1)

Application NumberPriority DateFiling DateTitle
ES441470AES441470A1 (en)1975-10-031975-10-03Obtaining procedure of 1- (2-hydroxymethyl-1-fenoxy) -2-pharmacologically active propanolamines. (Machine-translation by Google Translate, not legally binding)

Applications Claiming Priority (1)

Application NumberPriority DateFiling DateTitle
ES441470AES441470A1 (en)1975-10-031975-10-03Obtaining procedure of 1- (2-hydroxymethyl-1-fenoxy) -2-pharmacologically active propanolamines. (Machine-translation by Google Translate, not legally binding)

Publications (1)

Publication NumberPublication Date
ES441470A1true ES441470A1 (en)1977-04-01

Family

ID=8470099

Family Applications (1)

Application NumberTitlePriority DateFiling Date
ES441470AExpiredES441470A1 (en)1975-10-031975-10-03Obtaining procedure of 1- (2-hydroxymethyl-1-fenoxy) -2-pharmacologically active propanolamines. (Machine-translation by Google Translate, not legally binding)

Country Status (1)

CountryLink
ES (1)ES441470A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
EP0714883A1 (en)*1994-12-021996-06-05Bristol-Myers Squibb CompanyAryloxypropanolamine beta 3 adrenergic agonists

Cited By (1)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
EP0714883A1 (en)*1994-12-021996-06-05Bristol-Myers Squibb CompanyAryloxypropanolamine beta 3 adrenergic agonists

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