CA2341458A1 - Aminoalcohol derivatives and their use as beta 3 adrenergic agonists - Google Patents

Aminoalcohol derivatives and their use as beta 3 adrenergic agonists Download PDF

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Publication number
CA2341458A1
CA2341458A1 CA002341458A CA2341458A CA2341458A1 CA 2341458 A1 CA2341458 A1 CA 2341458A1 CA 002341458 A CA002341458 A CA 002341458A CA 2341458 A CA2341458 A CA 2341458A CA 2341458 A1 CA2341458 A1 CA 2341458A1
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Prior art keywords
amino
alkyl
phenyl
hydroxy
bis
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CA002341458A
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French (fr)
Inventor
Kiyoshi Taniguchi
Naoaki Fujii
Minoru Sakurai
Yasuyo Tomishima
Hisashi Takasugi
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Fujisawa Pharmaceutical Co Ltd
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Individual
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
    • C07C323/24—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C323/25—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C215/04—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated
    • C07C215/06—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and acyclic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/46—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C215/48—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups
    • C07C215/54—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C217/28—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having one amino group and at least two singly-bound oxygen atoms, with at least one being part of an etherified hydroxy group, bound to the carbon skeleton, e.g. ethers of polyhydroxy amines
    • C07C217/30—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having one amino group and at least two singly-bound oxygen atoms, with at least one being part of an etherified hydroxy group, bound to the carbon skeleton, e.g. ethers of polyhydroxy amines having the oxygen atom of at least one of the etherified hydroxy groups further bound to a carbon atom of a six-membered aromatic ring
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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
    • C07C217/58—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms with amino groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
    • C07C217/60—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms linked by carbon chains having two carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
    • C07C217/62—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C217/64—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by singly-bound oxygen atoms
    • C07C217/66—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by singly-bound oxygen atoms with singly-bound oxygen atoms and six-membered aromatic rings bound to the same carbon atom of the carbon chain
    • C07C217/72—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by singly-bound oxygen atoms with singly-bound oxygen atoms and six-membered aromatic rings bound to the same carbon atom of the carbon chain linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
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    • C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/78—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
    • C07C217/80—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings
    • C07C217/82—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring
    • C07C217/84—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
    • C07C217/86—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical containing six-membered aromatic rings
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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/34—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/38—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to acyclic carbon atoms and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
    • C07C233/42—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C07C233/43—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of a saturated carbon skeleton
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    • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C237/08—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
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    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/26—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
    • C07C271/28—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
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    • C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
    • C07C311/28—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
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    • C07C317/00—Sulfones; Sulfoxides
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    • C07C317/32—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • C07C317/34—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having sulfone or sulfoxide groups and amino groups bound to carbon atoms of six-membered aromatic rings being part of the same non-condensed ring or of a condensed ring system containing that ring
    • C07C317/36—Sulfones; Sulfoxides having sulfone or sulfoxide groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton with sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having sulfone or sulfoxide groups and amino groups bound to carbon atoms of six-membered aromatic rings being part of the same non-condensed ring or of a condensed ring system containing that ring with the nitrogen atoms of the amino groups bound to hydrogen atoms or to carbon atoms
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    • C07C323/32—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton having at least one of the nitrogen atoms bound to an acyclic carbon atom of the carbon skeleton
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    • C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated

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Abstract

This invention relates to new aminoalcohol derivatives or salts thereof represented by formula (I) wherein each symbol is as defined in the specification or salts thereof which have .beta.3 adrenergic agonist activit y and therefore have gut selective sympathomimetic, anti-ulcerous, anti- pancreatitis, lipolytic, anti-urinary incontinence and anti-pollakiuria activities, to processes for the preparation thereof, to a pharmaceutical composition comprising the same and to a method for the prevention and/or treatment of diseases indicated in the specification to a human being or an animal.

Description

DESCRIPTION
NEW COMPOUND
TECHNICAL FIELD
This invention relates to new aminoalcohol derivatives and salts thereof which are ~3 adrenergic receptor agonists and useful as a medicament.
DISCLOSURE OF INVENTION ' This invention relates to new aminoalcohol derivatives which are ~3 adrenergic receptor agonists and salts thereof.
More particularly, it relates to new aminoalcohol derivatives and salts thereof which have gut selective sympathomimetic, anti-ulcerous, anti-pancreatitis, lipolytic, anti-urinary incontinence and anti-pollakiuria activities, to processes for the preparation thereof, to a pharmaceutical composition comprising the same and to a method of using the same therapeutically in the treatment and/or prevention of gastro-intestinal disorders caused by smooth muscle contractions in human beings or animal.
One object of this invention is to provide new and useful aminoalcohol derivatives and salts thereof which have gut selective sympathomimetic, anti-ulcerous, lipolytic, anti-urinary incontinence and anti-pollakiuria activities.
Another object of this invention is to provide processes for the preparation of said aminoalcohol derivatives and salts thereof.
A further object of this invention is.to provide a pharmaceutical composition comprising, as an active ingredient, said aminoalcohol derivatives and salts thereof.
Still further object of this invention is to provide a therapeutical method for the treatment and/or prevention of aforesaid diseases in human beings or animals, using said aminoalcohol derivatives and salts thereof.
The object aminoalcohol derivatives of this invention are new and can be represented by the following general formula [I] .

i A-X-~H-CH2-N-Z-Y [I~
~R4 wherein A is a heterocyclic group or aryl, each of which may have 1 to 3 same or different substituent(s) selected from a group consisting of halogen, hydroxy, amino, lower alkyl, lower alkylsulfonylamino, phenyl(lower)alkoxy and phenyl(lower)alkoxycarbonylamino, -X- is bond, -CH2-, -CH2-CH2-, -NH-CH2-, -0-CH2-, -S-CH2-, -SO-CH2- or -S02-CH2-, -Y~ is -C ' (in which R11 is hydrogen, hydroxy, ~11 lower alkoxy or acyloxy) and -Z- is -(CH2)n-~-(CH2)m-~-(CH2)k-, -(CH2)n ~ C.\ (CH2)m-, ~7 ~9 (CH2) r /( CH2 ) p.~
-(CH2)n-Q-(CH2)m-, -(CH2)n-CH CH-(CH2)m-~
~( CH2 ) q~
-(CH2)n-CH=CH-(CH2)m- or -(CH2)n-C=C-(CH2)m- (in which -Q- is -O-, -S-, -SO-, -S02-, -N-CO-, -CO-N-, ~10 R10 -CH-CO-N-, -CH-CH2-N-, -S02-N-, -N-S02-, -CO- or -N-, wherein R10 is hydrogen or ~10 ~10 lower alkyl, and R11 is lower alkyl, R6, R~, Rg and R9 are each independently hydrogen, hydroxy, lower alkyl, lower alkenyl, lower alkoxy, lower alkoxy(lower)alkyl or aryl which may have 1 to 3 lower alkoxy, n, m and k is each independently 0 to 6, p is 0 to 4, q is 1 to 4, and r is 2 to 7) and -Z-Y~ is -(CH2)i-CH=C~ (in which i is 0 to 6), R1 is hydrogen or an amino protective group, and R2, R3, R4 and R5 are each independently hydrogen;
lower alkyl; lower alkylthio; lower alkylsulfonyl;
hydroxy; lower alkoxy;
amino; lower alkylamino; acylamino; N-(lower alkyl)acylamino; carboxy; lower alkoxycarbonyl;
carbamoyl optionally substituted with one or two lower alkyl; hydroxy(lower)alkyl; lower alkoxy(lower)alkyl;
N-acylamino(lower)alkyl; N-(lower alkyl)-N-acylamino(lower)alkyl; carboxy(lower)alkyl;
lower alkoxycarbonyl(lower)alkyl; carbamoyl(lower)alkyl optionally substituted with one or two lower alkyl; or -(CH2)j-N ~R13 (in which R12 and R13 are each independently hydrogen or lower alkyl, or R12 and R13 may be bonded to form a lower alkylene chain, and j is 0 to 6) .
The object. compound [I] or a salt thereof can be prepared by the following processes.
Process 1 o R1 A-X-C CH2 + HN-Z-Y
[II]

or a salt thereof R5 [III]
or a salt thereof i A-X-~H-CH2-N-Z-Y

[I]
or a salt thereof Dr~~occ '7 i OH Ra ~R4 [Ia]
or a salt thereof elimination reaction R3 ~i of amino protective OH H
group A-X-~H-CH2-N-Z-Y
~R4 [Ib]
or a salt thereof wherein A, X, Y, Z, R1, R2, R3, R4 and R5 are each as defined above, and Ra is an amino protective group.
5 In the above and subsequent description of the present specification, suitable examples of the various definition to be included within the scope of the invention are explained in detail in the following.
The term "lower" is intended to mean a group having 1 to 6 carbon atom(s), unless otherwise provided.
Suitable example of "lower alkyl" and "lower alkyl"
moiety may include straight or branched one having 1 to 6 carbon atom(s), such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, 1-methylpentyl, tert-pentyl, neo-pentyl, hexyl, isohexyl and the like.
Suitable "lower alkenyl" may include vinyl, 1-(or 2-)propenyl, 1-(or 2- or 3-)butenyl, 1-(or 2- or 3- or 4-)pentenyl, 1-(or 2- or 3- or 4- or 5-)hexenyl, methylvinyl, ethylvinyl, 1-(or 2- or 3-)methyl-1-(or 2-)propenyl, 1-(or 2-or 3-)ethyl-1-(or 2-)propenyl, 1-(or 2- or 3- or 9-)methyl-1-(or 2- or 3-)butenyl, and the like, in which more preferable example may be C2-C4 alkenyl.
Suitable "lower alkoxy" and "lower alkoxy" moiety may be a straight or branched one such as methoxy, ethoxy, propoxy, isopropoxy, 1-ethylpropoxy, butoxy, sec-butoxy, tert-butoxy, pentyloxy, neopentyloxy, tert-pentyloxy, hexyloxy, and the like, in which the preferred one may be C1-C4 alkoxy, and the most preferred one may be methoxy.
Suitable example of "halogen" may be fluoro, chloro, bromo and iodo.
Suitable example of "aryl" and "ar" moiety may include phenyl, naphthyl, anthryl, and the like, in which the preferred one may be phenyl.
Suitable example of "heterocyclic group" may include unsaturated 3 to 8-membered (more preferably 5 or 6-membered) heteromonocyclic group containing 1 to 4 nitrogen atom(s), for example, pyrrolyl, pyrrolinyl, imidazolyl, pyrazolyl, pyridyl, dihydropyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazolyl (e. g., 4H-1,2,4-triazolyl, 1H-1,2,3-triazolyl, 2H-1,2,3-triazolyl, etc.), tetrazolyl (e.g., 1H-tetrazolyl, 2H-tetrazolyl, etc.), etc.;
saturated 3 to 8-membered (more preferably 5 or 6-membered) heteromonocyclic group containing 1 to 4 nitrogen atom(s), for example, pyrrolidinyl, imidazolidinyl, piperidyl, piperazinyl, etc.;
unsaturated condensed heterocyclic group containing 1 to 4 nitrogen atom(s), .for example, indolyl, isoindolyl, indolinyl, indolizinyl, benzimidazolyl, quinolyl, isoquinolyl, indazolyl, benzotriazolyl, etc.;
unsaturated 3 to 8-membered (more preferably 5 or 6 membered) heteromonocyclic group containing 1 to 2 oxygen atoms) and 1 to 3 nitrogen atom(s), for example, oxazolyl, isoxazolyl, oxadiazolyl (e. g., 1,2,4-oxadiazolyl, 1,3,4-oxadiazolyl, 1,2,5-oxadiazolyl, etc.), etc.;
saturated 3 to 8-membered (more preferably 5 or 6-membered) heteromonocyclic group containing 1 to 2 oxygen atoms) and 1 to 3 nitrogen atom(s), for example, morpholinyl, sydnonyl, etc.;
unsaturated condensed heterocyclic group containing 1 to 2 oxygen atoms) and 1 to 3 nitrogen atom(s), for example, benzoxazolyl, benzoxadiazolyl, etc.;
unsaturated 3 to 8-membered (more preferably 5 or 6-membered) heteromonocyclic group containing 1 to 2 sulfur atoms) and 1 to 3 nitrogen atom(s), for example, thiazolyl, isothiazolyl, thiadiazolyl (e. g., 1,2,3-thiadiazolyl, 1,2,4-thiadiazolyl, 1,3,4-thiadiazolyl, 1,2,5-thiadiazolyl, etc.), dihydrothiazinyl, etc.;
saturated 3 to 8-membered (more preferably 5 or 6-membered) heteromonocyclic group containing 1 to 2 sulfur atoms) and 1 to 3 nitrogen atom(s), for example, thiazolidinyl, etc.;
unsaturated 3 to 8-membered (more preferably 5 or 6-membered) heteromonocyclic group containing 1 to 2 sulfur atom(s), for example, thienyl, dihydrodithiinyl, dihydrodithionyl, etc.;
unsaturated condensed heterocyclic group containing 1 to 2 sulfur atoms) and 1 to 3 nitrogen atom(s), for example, benzothiazolyl, benzothiadiazolyl, imidazothiadiazolyl, etc.;
unsaturated 3 to 8-membered (more preferably 5 or 6-membered) heteromonocycli.c group containing an oxygen atom, for example, furyl, etc.;
saturated 3 to 8-membered (more preferably 5 or 6-membered) heteromonocyclic group containing an oxygen atom, for example, tetrahydrofuran, tetrahydropyran, etc.;
unsaturated 3 to 8-membered (more preferably 5 or 6-membered) heteromonocyclic group containing an oxygen atom and 1 to 2 sulfur atom(s), for example, dihydrooxathiinyl, etc.;
unsaturated condensed heterocyclic group containing 1 to 2 sulfur atom(s), for example, benzothienyl, benzodithiinyl, etc.;
unsaturated condensed heterocyclic group containing an oxygen atom and 1 to 2 sulfur atom(s), for example, benzoxathiinyl, etc.;
2-oxo-2,3-dihydro-1H-benzimidazolyl; and the like.
Suitable example of "amino protective group" moiety may be common amino protective group such as acyl, for example, substituted or unsubstituted lower alkanoyl [e. g. formyl, acetyl, propionyl, trifluoroacetyl, etc.], phthaloyl, lower alkoxycarbonyl [e. g. tert-butoxycarbonyl, tert-amyloxy-carbonyl, etc.], substituted or unsubstituted aralkyloxy-carbonyl [e. g. benzyloxycarbonyl, p-nitrobenzyloxycarbonyl, etc.], substituted or unsubstituted arenesulfonyl [e. g.
benzenesulfonyl, tosyl, etc.], nitrophenylsulfenyl, ar(lower)alkyl [e.g. trityl, benzyl, etc.], and the like, in which preferable one is phenyl(lower)alkyl such as benzyl.
Suitable "acyl" and "acyl" moiety may be carboxy;
esterified carboxy; carbamoyl optionally substituted with one or two lower alkyl; lower alkylsulfonyl [e. g. methylsulfonyl, ethylsulfonyl, propylsulfonyl, butylsulfonyl, pentylsulfonyl, hexylsulfonyl, etc.]; substituted or unsubstituted lower alkanoyl [e. g. formyl, acetyl, trifluoroacetyl, propanoyl, butanoyl, 2-methylpropanoyl, pentanoyl, 2,2-dimethylpropanoyl, hexanoyl, etc.]; and the like.
The esterified carboxy may be substituted or unsubstituted lower alkoxycarbonyl [e. g. methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, butoxycarbonyl, hexyloxycarbonyl, 2-iodoethoxycarbonyl, trifluoromethoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, .
etc.], substituted or unsubstituted aryloxycarbonyl [e. g.
phenoxycarbonyl, 4-nitrophenoxycarbonyl, 2-naphthyloxycarbonyl, etc.], substituted or unsubstituted ar(lower)alkoxycarbonyl [e. g. benzyloxycarbonyl, phenethyloxycarbonyl, benzhydryloxycarbonyl, 4-nitrobenzyloxycarbonyl, etc.] and the like, in which the preferred one may be lower alkoxycarbonyl, and the most preferred one may be ethoxycarbonyl.
Suitable example of "lower alkylsulfonylamino" may include methylsulfonylamino, ethylsulfonylamino, propylsulfonylamino, butylsulfonylamino, pentylsulfonylamino, hexylsulfonylamino, and the like, in which the preferred one may be (Cl-C4)alkylsulfonylamino, and the most preferred one may be methylsulfonylamino.
Suitable example of "heterocyclic group" in A can be referred to aforementioned "heterocyclic group", in which the preferred one may be unsaturated 3 to 8-membered (more preferably 5 or 6-membered) heteromonocyclic group containing 1 to 4 nitrogen atoms) or unsaturated condensed heterocyclic group containing 1 to 4 nitrogen atom(s), and the most preferred one may be pyridyl, indolyl or 2-oxo-2,3-dihydro-1H-benzimidazolyl.
The lower alkylene chain formed by R~ and R8 is a straight or branched chain alkylene having 1 to 6 carbon atoms and is exemplified by methylene, ethylene, trimethylene, propylene, butylene, 1,2-dimethylethylene, pentamethylene and hexamethylene.
Preferred embodiments of the object compound [I] are as follow:
A is pyridyl, indolyl, 2-oxo-2,3-dihydro-1H-benzimidazolyl or phenyl, each of which may have 1 to 3 same or different substituent(s) selected from a group of hydroxy, amino lower alkyl (more preferably methyl), lower alkylsulfonylamino (more preferably methanesulfonylamino), phenyl(lower)alkoxy (more preferably benzyloxy) and phenyl(lower)alkoxycarbonylamino (more preferably benzyloxycarbonylamino), -X- is bond, -CH2-, -CH2-CH2-, -O-CH2- or -S02-CH2-, -Y~ is -C ~ (in which R11 is hydrogen or hydroxy) and -Z- is -(CH2)n-i-(CH2)m-i-(CH2)k-, -(CH2)ri ~C ~ (CH2)m- or R7 R9 (CH2 ) r -(CH2)n-Q-(CH2)m- (in which -Q- is -CH-CO-N- or -CH-CHZ-N-, wherein ~11 ~10 ~11 ~10 R10 is hydrogen or lower alkyl (more preferably methyl) and R11 is lower alkyl (more preferably methyl), R6, R~, R8 and R9 are each independently hydrogen, 10 lower alkyl (more preferably methyl) or aryl (more preferably phenyl) which may have 1 to 3 lower alkoxy (more preferably methoxy), n, m and k is each independently 0 to 6, and r is 2 to 7) and -Z-Y~ is -(CH2)i-CH=C~ (in which i is 0 to 6), R1 is hydrogen or ar(lower)alkyl (more preferably benzyl), and R2, R3, R4 and R5 are each independently hydrogen;
lower alkyl (more preferably methyl); lower alkylthio (more preferably methylthio); lower alkylsulfonyl (more preferably methanesulfonyl); hydroxy; lower alkoxy (more preferably methoxy or ethoxy);
amino; lower alkylamino (more preferably methylamino);
acylamino (more preferably lower alkoxycarbonylamino, lower alkylsulfonylamino, lower alkanoylamino, ureido or trifluoroacetylamino, most preferably methoxycarbonylamino, ethoxycarbonylamino, methanesulfonylamino, formylamino, acetylamino or propionylamino); N-(lower alkyl)acylamino [more preferably N-(lower alkyl)-[(lower)alkoxycarbonyl]amino, most preferably N-methyl-methoxycarbonylamino]; carboxy;
or lower alkoxycarbonyl (more preferably methoxycarbonyl).
More preferred embodiments of the object compound [I]
are as follow:
A is phenyl each of which may have 1 to 3 same or different substituent(s) selected from a group of hydroxy, amino, lower alkylsulfonylamino (more preferably methanesulfonylamino) and phenyl(lower)alkoxy (more preferably benzyloxy), -X- is bond, -CH2-, -CH2-CH2-, -0-CH2- or -S02-CH2-, -Y~ is -C ~ (in which R11 is hydrogen or hydroxy), R6 Rg -Z- is -(CH2)n-~-(CH2)m-~-(CH2)k- (in which R~ R9 R6, R~, R8 and R9 are each independently hydrogen, lower alkyl (more preferably methyl) or phenyl which may have 1 to 3 lower alkoxy (more preferably methoxy), n, m and k is each independently 0 or 1), R1 is hydrogen or phenyl(lower)alkyl (more preferebly benzyl), and R2, R3, R4 and R5 are each independently hydrogen; lower alkyl (more preferably methyl); lower alkylthio (more preferably methylthio); lower alkylsulfonyl (more preferably methanesulfonyl); hydroxy; lower alkoxy (more preferably methoxy or ethoxy); amino; lower alkylamino (more preferably methylamino); lower alkoxycarbonylamino (more preferably methoxycarbonylamino or ethoxycarbonylamino); lower alkylsulfonylamino (more preferably methanesulfonylamino); lower alkanoylamino (more preferably formylamino, acetylamino or propionylamino); ureido; trifluoroacetylamino; N-(lower alkyl)-[(lower)alkoxycarbonyl]amino (more preferably N-methyl-methoxycarbonylamino); carboxy; or lower alkoxycarbonyl (more preferably methoxycarbonyl).
Suitable salts of the object arninoalcohol derivatives [I] are pharmaceutically acceptable salts and include conventional non-toxic salts such as an inorganic acid addition salt [e. g. hydrochloride, hydrobromide, sulfate, phosphate, etc.], an organic acid addition salt [e. g.
formate, acetate, trifluoroacetate, oxalate, maleate, fumarate, tartrate, methanesulfonate, benzenesulfonate, toluenesulfonate, etc.], an alkali metal salt [e. g. sodium salt, potassium salt, etc.] or the like.
The processes for preparing the object compound [I] are explained in detail in the following.
Process 1 The object compound [I] or a salt thereof can be prepared by reacting a compound [II] with a compound [III] or a salt thereof.
Suitable salt of the compound [III] may be the same as those exemplified for the compound [I].
The reaction is preferably carried out in the presence of a base such as an alkali metal carbonate [e. g. sodium carbonate, potassium carbonate, etc.], an alkaline earth metal carbonate [e. g. magnesium carbonate, calcium carbonate, etc.], an alkali metal bicarbonate [e. g. sodium bicarbonate, potassium bicarbonate, etc.], tri(lower)alkylamine [e. g.
trimethylamine, triethylamine, etc.], picoline or the like.
The reaction is usually carried out in a conventional solvent, such as an alcohol [e. g. methanol, ethanol, propanol, isopropanol, etc.], diethyl ether, tetrahydrofuran, dioxane, or any other organic solvent which does not adversely influence the reaction.
The reaction temperature is not critical, and the reaction can be carried out under cooling to heating.
Process 2 The object compound [Ib] or a salt thereof can be prepared by subjecting a compound [Ia] or a salt thereof to elimination reaction of the amino protective group.
Suitable salts of the compounds [Ia] and [Ib] may be the same as those exemplified for the compound [I].
This reaction is carried out in accordance with a conventional method such as hydrolysis, reduction or the like.
The hydrolysis is preferably carried out in the presence of a base or an acid including Lewis acid.
Suitable base may include an inorganic base and an organic base such as an alkali metal [e. g. sodium, potassium, etc.], an alkaline earth metal [e. g. magnesium, calcium, etc.], the hydroxide or carbonate or bicarbonate thereof, hydrazine, trialkylamine [e. g. trimethylamine, triethylamine, etc.], picoline, 1,5-diazabicyclo[4.3.0]non-5-ene, 1,4-diazabicyclo[2.2.2]octane, 1,8-diazabicyclo[5.9.0]undec-7-ene, or the like.
Suitable acid may include an organic acid [e. g. formic acid, acetic acid, propionic acid, trichloroacetic acid, trifluoroacetic acid, etc.], an inorganic acid [e. g.
hydrochloric acid, hydrobromic acid, sulfuric acid, hydrogen chloride, hydrogen bromide, hydrogen fluoride, etc.] and an acid addition salt compound [e. g. pyridine hydrochloride, etc. ] .
The elimination using trihaloacetic acid [e. g.
trichloroacetic acid, trifluoroacetic acid, etc.] or the like is preferably carried out in the presence of cation trapping agents [e.g. anisole, phenol, etc.].
The reaction is usually carried out in a solvent such as water, an alcohol [e. g. methanol, ethanol, etc.], methylene chloride, chloroform, tetrachloromethane, tetrahydrofuran, a mixture thereof or any other solvent which does not adversely influence the :reaction. A liquid base or acid can be also used as the solvent. The reaction temperature is not critical and the reaction is usually carried out under cooling to heating.
The reduction method applicable for the elimination reaction may include chemical reduction and catalytic reduction.
Suitable reducing agents to be used in chemical reduction are a combination of metal (e. g. tin, zinc, iron, etc.] or metallic compound [e. g. chromium chloride, chromium acetate, etc.] and an organic or inorganic acid [e. g. formic acid, acetic acid, propionic acid, trifluoroacetic acid, p-toluenesulfonic acid, hydrochloric acid, hydrobromic acid, etc.].
Suitable catalysts to be used in catalytic reduction are conventional ones such as platinum catalysts [e. g. platinum plate, spongy platinum, platinum black, colloidal platinum, platinum oxide, platinum wire, etc.], palladium catalysts [e. g. spongy palladium, palladium black, palladium oxide, palladium on carbon, colloidal palladium, palladium on barium sulfate, palladium on barium carbonate, etc.], nickel catalysts [e. g. reduced nickel, nickel oxide, Raney nickel, etc.], cobalt catalysts [e. g. reduced cobalt, Raney cobalt, etc.], iron catalysts [e.g. reduced iron, Raney iron, etc.], copper catalysts [e. g. reduced copper, Raney copper, Ullman copper, etc.] and the like.
In case that the amino protective group is benzyl, the reduction is preferably carried out in the presence of a combination of palladium catalysts [e. g. palladium black, palladium on carbon, etc.] and formic acid or its salt [e. g.
ammonium formate, etc.].
The reduction is usually carried out in a conventional solvent which does not adversely influence the reaction such as water, an alcohol [e. g. methanol, ethanol, propanol, etc.], chlorobenzene, N,N-dimethylformamide, or a mixture thereof. Additionally, in case that the above-mentioned acids to be used in chemical reduction are in liquid, they can also be used as a solvent. Further, a suitable solvent to be used in catalytic reduction may be the above-mentioned solvent, and other conventional solvent such as diethyl ether, dioxane, tetrahydrofuran, etc. or a mixture thereof.
5 The reaction temperature of this reduction is not critical and the reaction is usually carried out under cooling to heating.
The compounds obtained by the above processes can be 10 isolated and purified by a conventional method such as pulverization, recrystallization, column chromatography, reprecipitation, or the like, and converted to the desired salt in conventional manners, if necessary.
It is to be noted that the compound [I] and the other 15 compounds may include one or more stereoisomers due to asymmetric carbon atoms, and all of such isomers and mixture thereof are included within the scope of this invention.
It is further to be noted that isomerization or rearrangement of the object compound [I] may occur due to the effect of the light acid, base or the like, and the compound obtained as the result of said isomerization or rearrangement is also included within the scope of the present invention.
It is also to be noted that the solvating form of the compound [I] (e. g. hydrate, etc.) and any form of the crystal of the compound [I] are included within the scope of the present invention.
The object compound [I] or a salt thereof possesses gut selective sympathomimetic, anti-ulcerous, anti-pancreatitis, lipolytic and anti-pollakiuria activities, and are useful for the treatment and/or prevention of gastro-intestinal disorders caused by smooth muscle contractions in human beings or animals, and more particularly to methods for the treatment and/or prevention of spasm or hyperanakinesia in case of irritable bowel syndrome, gastritis, gastric ulcer, duodenal ulcer, enteritis, cholecystopathy, cholangitis, urinary calculus and the like; for the treatment and/or prevention of ulcer such as gastric ulcer, duodenal ulcer, peptic ulcer, ulcer causes by non steroidal anti-inflammatory drugs, or the like; for the treatment and/or prevention of dysuria such as pollakiuria, urinary incontinence or the like in case of nervous pollakiuria, neurogenic bladder dysfunction, nocturia, unstable bladder, cystospasm, chronic cystitis, chronic prostatitis, prostatic hypertrophy or the like; and for the treatment and/or prevention of pancreatitis, obesity, diabetes, glycosuria, hyperlipidemia, hypertension, atherosclerosis, glaucoma, melancholia, depression or the like; and for the treatment and/or prevention of diseases as the result of insulin resistance (e. g. hypertension, hyperinsulinemia, etc.), and the like.
In order to show the usefulness of the compound [I] for the prophylactic anc therapeutic treatment of above-mentioned disease in human beings or animals, the pharmacological test data of a representative compound thereof are shown in the following.
Test Effect on the increase in intravesical pressure induced by carbachol in anesthetized dog Test Compouund (1) (2S)-1-[[(2RS)-4,9-bis(4-hydroxyphenyl)-2-butyl]amino]-3-phenoxy-2-propanol hydrochloride Test Method Female Beagle dogs weighing 8.0-15.0 kg were fasted for 24 hours and maintained under halothane anesthesia. A 12F
Foley catheter was lubricated with water soluble jelly, inserted into the urethral orifice and advanced approximately cm until the balloon tip was placed well inside the bladder. The balloon was then inflated with 5 ml of room air and catheter slowly withdrawn just part the first resistance that is felt at the bladder neck. Urine was completely 5 drained out through the catheter, and 30 ml of biological saline was infused. The catheter was connected to pressure transducer, and intravesical pressure was continuously recorded. The test compound was injected intravenously at 5 minutes before the administration of carbachol (1.8 ~g/kg).
Test Results Treatment Increase in intravesical pressure (mmHg) Control 4.5 ~ 0.3 Test Compound (1) **
2.5 ~ 0.3 (0.01 mg/kg) **P<0.01 vs Control (ANOVA) (N=3) The following Preparations and Examples are given for the purpose of illustrating this invention.
Example 1 A solution of (2S)-3-phenoxy-1,2-epoxypropane (195 mg) (IL FARMACO, 50 (10), 643 (1995)) and 4,4-bis(4-hydroxyphenyl)-2-butylamine (257 mg) in ethanol (2 ml) was stirred under reflux for 24 hours and evaporated in vacuo.
The residue was chromatographed (chloroform-methanol) over silica gel (9 g) and the eluate was treated with 4N hydrogen chloride in ethyl acetate to afford a crude oil, which was powdered from diethyl ether to afford (2S)-1-[[(2RS)-4,4-bis(4-hydroxyphenyl)-2-butyl]amino]-3-phenoxy-2-propanol hydrochloride (117 mg) as a pale brown powder.
mp . 73°C (dec.) IR (Nujol) . 3600-3100, 2700-2400, 1230 cm-1 NMR (DMSO-d6, d) . 1.21-1.27 (3H, m, CH3), 1.94 (1H, m, CH2), 2.60 (1H, m, CH2), 2.85-3.2 (3H, m, CH2NCH), 3.95 (1H, m, CHAr2), 4.01-4.05 (2H, m, ArOCH2), 4.16 (1H, m, CH_OH), 5.85 (1H, br s, OH), 6.64-6.72 (4H, m, aromatic H), 6.92-7.16 (7H, m, aromatic H), 7.26-7.35 (2H, m, aromatic H), 8.62 (1H, br, NH), 8.92 (1H, br, HC1), 9.23 (1H, br s, OH), 9.28 (1H, br s, OH) MS m/z . 408 (M++1) Example 2 (2R)-N-Benzyl-4,4-bis(4-methoxyphenyl)-2-butylamine hydrochloride (412 mg) was converted to the corresponding free base in a usual manner. 1.OM Solution of tin(IV) chloride in dichlo.romethane (1.5 ml) was added dropwise to a stirred solution of the free base and (2S)-3-phenoxy-1,2-epoxypropane (225 mg) (IL FARMACO, 50 (10), 643 (1995)) in dichloromethane (4 ml) at -10 - -5°C under a nitrogen atmosphere over 10 minutes and the resulting mixture was stirred for 1.5 hours at the same temperature. The reaction mixture was poured into 1N hydrochloric acid and the mixture was stirred under ice cooling for 20 minutes. The organic layer was separated, washed with an aqueous solution of sodium fluoride and a saturated aqueous solution of sodium bicarbonate, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed (ethyl acetate) over silica gel (11 g) and the eluate was treated with 4N hydrogen chloride in ethyl acetate to afford (2S)-1-[N-benzyl-[(2R)-4,4-bis(4-methoxyphenyl)-2-butyl)amino]-3-phenoxy-2-propanol hydrochloride (136 mg) as an oil.
IR (Film) . 3292, 2850-2400, 1243 cm-1 NMR (CDC13, ~) . 1.27 and 1.47 (3H, each d, J=6.2 and 6.6Hz), 2.08 (1H, m), 2.9-3.5 (4H, m), 3.68-4.0 (2H, m), 3.74, 3.75 and 3.76 (6H, each s), 4.02-4.08 (2H, m), 4.10-4.26 (1H, m), 4.3-4.6 (1H, m), 6.72-7.43 and 7.64-7.68 (18H, m) MS m/z . 526 (M++1) _Example 3 (2S)-N-Benzyl-9,4-bis(4-methoxyphenyl)-2-butylamine hydrochloride (412 mg) was converted to the corresponding free base in a usual manner. A solution of the free base and (2S)-3-phenoxy-1,2-epoxypropane (195 mg) (IL FARMACO, 50 (10), 643 (1995)) in ethanol (4 ml) was stirred under reflux for 10 hours, cooled to room temperature, and evaporated in vacuo. The residue was chromatographed (chloroform) over silica gel and the eluate was treated with 4N hydrogen chloride in ethyl acetate to afford (2S)-1-[N-benzyl-[(2S)-4,4-bis(4-methoxyphenyl)-2-butyl]amino]-3-phenoxy-2-propanol hydrochloride (549 mg) as an amorphous powder.
[a]D4 . -22.59° (c=0.54, MeOH) IR (KBr) . 3300 (br), 2850-2400, 1248 cm-1 NMR (CDC13, d) . 1.41 and 1.56 (3H, each d, J=6.6Hz), 1.64 and 2.05 (1H, m), 2.94-3.6 (4H, m), 3.74, 3.75, 3.76 and 3.77 (6H, each s), 3.87-3.96 (2H, m), 4.05-4.25 (3H, m), 4.5-4.65 and 4.8 (1H, m), 5.9 (1H, br), 6.69-6.98 (8H, m), 7.08-7.17 (4H, m), 7.22-7.41 (4H, m), 7.65-7.73 (2H, m) MS m/z . 526 (M++1) Example 4 A mixture of (2S)-1-[N-benzyl-[(2R)-4,4-bis(4-methoxyphenyl)-2-butyl]amino]-3-phenoxy-2-propanol hydrochloride (96 mg) and 10% Pd/C (50o wet, 60 mg) in methanol (4 ml} was stirred at room temperature in the presence of hydrogen at an atmospheric pressure for 6 hours and filtered. The filtrate was evaporated in vacuo and the residue was partitioned between dichloromethane and an aqueous solution of sodium bicarbonate. The organic layer was separated, dried over sodium sulfate, and evaporated in vacuo. The residue was chromatographed (dichloromethane-methanol) over silica gel (2 g) to afford an oil, which was converted to the corresponding oxalate in a usual manner to afford (2S)-1-[[(2R)-4,4-bis(4-methoxyphenyl)-2-butyl]amino]-3-phenoxy-2-propanol oxalate (1:1) (26 mg) as a colorless 5 powder.
mp . 121-123°C (from diethyl ether) IR (KBr) . 3423 (br), 2850-2650, 1734, 1701, 1633, 1603, 1250 cm-1 NMR (DMSO-d6, d) . 1.23 (3H, d, J=6.3Hz), 1.99 (1H, m), 10 2.58 (1H, m), 2.85-3.01 (2H, m), 3.11-3.17 (1H, m), 3.69 (3H, s), 3.71 (3H, s), 3.9-4.6 (8H, m), 6.81-6. 99 ( 7H, m) , 7 . 16-7 . 35 ( 6H, m) MS m/z . 436 (M++1) 15 Example 5 The following compound was obtained according to a similar manner to that of Example 4.
(2S)-1-[[(2S)-4,4-Bis(4-methoxyphenyl)-2-butyl]amino]-3-20 phenoxy-2-propanol oxalate (l: l) [a]D4 . 11.06° (c=0.515, MeOH) mp . 79-94°C (from diethyl ether) IR (KBr) . 3423 (br), 2750-2400, 1739-1691 (m), 1643, 1608, 1247 cm-1 NMR (DMSO-d6, d) . 1.25 (3H, d, J=6.3Hz), 1.96 (1H, m), 2.66 (1H, m), 2.86 (1H, m) 2.95-3.15 (2H, m), 3.69 (3H, s) , 3.70 (3H, s) , 3.94-4.15 (4H, m) , 5. 1 (4H, br), 6.81-6.88 (4H, m), 6.92-6.99 (3H, m), 7.17-7 . 35 ( 6H, m) MS m/z . 436 (M++1) Preparation 1 A mixture of methyl 3-aminobutyrate (4.3 g), (2S)-3-phenoxy-1,2-epoxypropane (4.59 g), ytterbium(III) trifluoromethanesulfonate (1.8 g) and dichloromethane (25 ml) was stirred at 40°C for 2. hours and at room temperature overnight, worked up in the usual manner and purified by silica gel column chromatography (toluene: ethanol:
concentrated ammonia water = 9:1:0.1) to give (3RS)-3-[((2S)-2-hydroxy-3-phenoxypropyl)amino]butyric acid methyl ester (2.59 g) .
IR (Neat): 3400 (br m), 1739 (s), 1599 (m), 1495 (m), 1458 (m), 1298 (m), 1246 (s), 1041 (m), 756 (m) cm-1 NMR (CDC13, d): 1.16 (3H, d, J=5.2Hz), 2.41-2.46 (2H, m), 2.6-3.0 (2H, m), 3.14 (1H, quartet, J=6.4Hz), 3.68 (3H, s), 3.9-4.1 (3H, m), 6.90-6.99 (3H, m), 7.24-7.33 (2H, m) MS m/z: 268 (M++1) _P_reparation 2 A mixture of (2S)-N-benzyl-(2-hydroxy-3-phenoxypropyl)amine (142 mg), 5-bromopentanoic acid ethyl ester (173 mg), potassium carbonate (153 mg) and N,N-dimethylformamide (2 ml) was stirred at 80°C for 4.5 hours, worked up in the usual manner and purified by silica gel column chromatography (20o ethyl acetate-hexane) to give (2S)-5-[N-benzyl-(2-hydroxy-3-phenoxypropyl)amino]pentanoic acid ethyl ester (93 mg).
NMR (CDC13, b): 1.25 (3H, t, J=7.lHz), 1.5-1.7 (5H, broad), 2.2-2.4 (2H, m), 2.4-2.8 (4H, m), 3.5-3.7 (1H, m), 3.7-3.9 (1H, m), 3.94 (2H, t, J=3.9Hz), 4.0-4.2 (1H, m), 4.12 (2H, quartet, J=7.lHz), 6.86-6.98 (4H, m), '7.2-7.4 (6H, m) MS m/z: 386 (M++1) _Pre aration 3 The following compound was obtained according to a similar manner to that of Preparation 2.
(2S)-4-[N-Benzyl-(2-hydroxy-3-phenoxypropyl)amino]-butanoic acid methyl ester IR (Neat) : 3482 (br m) , 2949 (m) , 1736 (s) , 1599 (w) , 1495 (m), 1456 (m), 1246 (s), 1041 (m), 754 (m), 696 (m) cm-1 NMR (CDC13, b): 1.88 (2H, quintet, J=7.lHz), 2.32 (2H, t, J=7.2Hz), 2.5-2.8 (4H, m), 3.5-3.7 (1H, m), 3.64 (3H, s) , 3. 84 (1H, d, J=13.OHz) , 3.89-4.0 (2H, m) , 4.0-4.2 (1H, m), 6.86-6.99 (4H, m), 7.2-7.4 (6H, m) MS m/z: 358 (M++1) Preparation 4 The following compounds were obtained according to a similar manner to that of Example 6.
(1) 1-[2,2-Bis(4-methoxyphenyl)-2-hydroxyethyl]cyclopentanol IR (KBr): 3347 (s), 3240 (m), 2958 (s), 1608 (m), 1510 (s), 1466 (m), 1248 (s), 1174 (m), 1034 (s), 835 (m) cm-1 NMR (CDC13, b): 1.2-1.7 (8H, m), 2.39 (1H, br s), 2.70 (2H, s) , 3.78 (6H, s) , 4.87 (1H, br s) , 6. 82 (4H, d, J=8.9Hz), 7.37 (4H, d, J=8.9Hz) (2) 3-(Dibenzylamino)-1,1-bis(4-bromophenyl)-1-propanol NMR (CDC13, ~): 2.3-2.4 (2H, m), 2.6-2.7 (2H, m), 3.51 (4H, s), 7.07 (2H, d, J=8.5Hz), 7.1-7.4 (16H, m) MS m/z: 564, 566 (M++1), 568 (3) (3RS)-3-(Dibenzylamino)-1,1-bis(9-bromophenyl)-1-butanol NMR (CDC13, b): 1.10 (3H, d, J=6.7Hz), 2.09 (1H, d, J=14.8Hz), 2.45 (1H, dd, J=11.2 and 14.8Hz), 3.1-3.3 (1H, m), 3.18 (2H, d, J=12.8Hz), 3.91 (2H, d, J=12.7Hz), 6.82 (2H, d, J=8.7Hz), 7.11 (2H, d, J=8.7Hz), 7.2-7.3 (12H, m), 7.40 (2H, d, J=9.9Hz) (4) (2S)-1-Phenoxy-3-[N-benzyl-[(3RS)-1,1-bis(4-bromophenyl)-1-hydroxy-3-butyl]amino]-2-propanol MS m/z: 638, 690 (M++1), 642 (5) N-Benzyl-[4,4-bis(4-methoxyphenyl)butyl]amine NMR (CDC13, b): 1.4-1.7 (2H, m), 2.00 (2H, quartet, J=7.8Hz), 2.64 (2H, t, J=7.lHz), 3.76 (6H, s), 3.72-3.79 (3H, m), 6.80 (4H, d, J=8.7Hz), 7.11 (4H, d, J=8.7Hz), 7.28 (5H, s) MS m/z: 376 (M++1) (6) N-Benzyl-[3,3-bis(4-ethoxyphenyl)propyl]amine MS m/z: 390 (M++1) Preparation 5 1-[2,2-Bis(4-methoxyphenyl)-2-hydroxyethyl]cyclopentanol (0.79 g) was hydrogenated in the usual manner to give 1-[2,2-bis(4-methoxyphenyl)ethyl]cyclopentanol (0.76 g).
IR (Neat): 3563 (m), 3448 (m), 2956 (s), 1610 (w), 1510 (s), 1460 (m), 1246 (s), 1178 (m), 1036 (s), 829 (m) cm-1 NMR (CDC13, g): 1.5-1.9 (9H, m), 2.40 (2H, d, J=7.3Hz), 3 . 77 ( 6H, s ) , 4 . 17 ( 1H, t, J=7 . 2Hz ) , 6 . 81 ( 4H, d, J=6.6Hz), 7.21 (4H, d, J=6.6Hz) Preparation 6 To a mixture of 1-[2,2-bis(4-methoxyphenyl)ethyl]-cyclopentanol (0.76 g), azidotrimethylsilane (0.32 g) and benzene (5 ml), boron trifluoride diethyl etherate (0.34 ml) was added dropwise at 0°C. The reaction mixture was stirred at room temperature for 30 minutes and worked up in the usual manner. The crude product was hydrogenated in the usual manner to give [1-[2,2-bis(4-methoxyphenyl)ethyl]-cyclopentyl]amine (0.74 g).
IR (Neat): 2949 (s), 1610 (m), 1510 (s), 1460 (m), 1248 (s), 1178 (m), 1038 (s), 829 (s) cm-1 NMR (CDC13, ~): 1.3-1.8 (lOH, m), 1.20 (2H, t, J=6.8Hz), 3.77 (6H, s), 4.09 (1H, quartet, J=6.8Hz), 6.81 (4H, dd, J=2.2 and 6.6Hz), 7.14 (4H, d, J=6.5Hz) MS m/z: 326 (M++1) Preparation 7 To a solution of dibenzylamine (1.14 g) and tetrahydrofuran (4 ml), butyllithium (1.54M in hexane, 3.7 ml) was added dropwise at -78°C under a flow of nitrogen.
After 30 minutes, a solution of 3-(3,4-dimethoxyphenyl)-acrylic acid methyl ester (1.06 g) in tetrahydrofuran (3 ml) was added dropwise, stirred for 1 hour and worked up in the usual manner. The crude product was purified by silica gel column chromatography (hexane: ethyl acetate = 5:1) to give 3-(dibenzylamino)-3-(3,4-dimethoxyphenyl)propionic acid methyl ester (0.53 g).
IR (Neat): 1739 (s), 1514 (s), 1458 (m), 1261 (m), 1146 (m) , 1028 (m) , 744 (m) cm-1 NMR (CDC13, b): 2.72 (1H, dd, J=7.3 and 14.4Hz), 3.07 (1H, dd, J=8.6 and 14.4Hz), 3.21 (1H, d, J=13.7Hz), 3.65 (3H, s), 3.73 (2H, s), 3.79 (2H, s), 3.89 (6H, s), 4.25 (1H, t, J=7.4Hz), 6.75-6.90 (3H, m), 7.1-7.4 (lOH, m) Preparation 8 A mixture of 3-(dibenzylamino)-3-(3,4-dimethoxyphenyl)-propionic acid methyl ester (0.53 g), acetic acid (3 ml), methanol (3 ml), and 20% palladium hydroxide on charcoal (0.05 g) was stirred under hydrogen (1 atm) at room temperature for 6 hours, filtered and evaporated to give 3-amino-3-(3,4-dimethoxyphenyl)propionic acid methyl ester acetate (0.24 g).
IR (KBr): 1729 (s), 1539 (s), 1523 (s), 1398 (m), 1265 (m), 1203 (m), 1155 (m), 1020 (m) cm-1 NMR (MeOH-d4, b): 1.90 (3H, s), 2.92 (2H, dd, J=5.4 and 6. 6Hz) , 3. 63 (3H, s) , 3. 82 (3H, s) , 3.84 (3H, s) , 4.52 (1H, t, J=7.5Hz) , 6. 95 (2H, s) , 7.02 (1H, s) 5 Preparation 9 To a solution of 3-aminopropionic acid methyl ester hydrochloride (1.12 g) in methanol (10 ml), 28% sodium methoxide-methanol solution (1.60 g) was added, filtered and evaporated. To the crude product, (2S)-2-phenoxy-1,2-10 epoxypropane (901 mg) and methanol (10 ml) were added and stirred under reflux for 2.5 hours. The reaction mixture was evaporated and purified by silica gel column chromatography to give 3-[((2S)-2-hydroxy-3-phenoxypropyl)amino]propionic acid methyl ester (0.76 g).
15 IR (KBr): 1734 (s), 1601 (m), 1498 (m), 1435 (m), 1252 (s), 1196 (m), 1043 (m), 752 (m) cm-1 NMR (CDC13, b): 2.54 (2H, t, J=6.4Hz), 2.72-2.98 (4H, m), 3.69 (3H, s), 3.97-4.07 (3H, m), 6.90-6.99 (3H, m), 7.25-7.32 (2H, m) 20 MS m/z: 254 (M++1) Preparation 10 The following compound was obtained according to a similar manner to that of Preparation 9.
(3RS)-3-[((2S)-2-Hydroxy-3-phenoxypropyl)amino]-3-phenylpropionic acid methyl ester IR (KBr): 1724 (s), 1599 (m), 1495 (m), 1435 (m), 1246 (s), 1126 (m), 1038 (m), 756 (m), 698 (m).cm-1 NMR (CDC13, b): 2.54-2.75 (4H, m), 3.66 (1.5H, s), 3.67 (1.5H, s), 3.9-4.0 (2H, m), 4.0-4.2 (2H, m), 6.85-6.98 (3H, m), 7.2-7.4 (7H, m) MS m/z: 330 (M++1) Preparation 11 To a mixture of N-carbobenzyloxy-D-alanine (0.81 g), [bis(4-methoxyphenyl)methyl]amine (0.80 g), 1-hydroxybenzotriazole (0.58 g) and N,N-dimethylformamide (5 ml), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.76 g) was added at 0°C and stirred at room temperature for 30 minutes. After a usual workup, N-carbobenzyloxy-D-alanine [bis(4-methoxyphenyl)methyl]amide (1.38 g) was obtained.
IR (KBr): 3296 (s), 1689 (m), 1647 (s), 1539 (s), 1512 (s), 1257 (s), 1176 (rn), 1031 (m) cm-1 NMR ( DMSO-d6, ~ ) : 1 . 21 ( 3H, d, J=7 . 1Hz ) , 3 . 33 ( 6H, s ) , 4.17 (1H, t, J=7.2Hz), 5.01 (2H, s), 5.96 (1H, d, J=8.4Hz), 6.86 (4H, d, J=8.7Hz), 7.1-7.2 (4H, m), 7.3-7.5 (5H, m), 8.60 (1H, d, J=8.5Hz) Preparation 12 To a solution of N-carbobenzyloxy-D-alanine [bis(4-methoxyphenyl)methyl]amide (0.33 g) in methanol and tetrahydrofuran (1:2, 10 ml), 50o wet 10°s palladium on charcoal was added and stirred under hydrogen atmosphere (1 atm) for 30 minutes. After a usual workup, D-alanine [bis(4-methoxyphenyl)methyl]amide (0.25 g) was obtained.
IR (Neat): 3357 (br s), 1678 (s), 1649 (s), 1538 (s), 1513 (s), 1259 (m), 1176 (m), 1032 (s), 831 (m), 812 (m) cm-1 NMR ( DMSO-d6, b ) : 1 . 13 ( 3H, d, J=6 . 9Hz ) , 3 . 33 ( 6H, s ) , 3.3-3.4 (3H, br) , 5.96 (1H, d, J=8.2Hz) , 6.87 (4H, d, J=8.7Hz), 7.15 (4H, d, J=8.4Hz), 8.44 (1H, d, J=8Hz) Preparation 13 To a solution of 4-methoxyphenylmagnesium bromide (1M in tetrahydrofuran, 35 ml) a solution of 3-(dibenzylamino)-propionic acid ethyl ester (4.87 g) in terahydrofuran (2 ml) was added, stirred under reflux for 1 hour, worked up in the usual manner and purified by silica gel column chromatography (hexane: ethyl acetate = 5:1) to give 3-dibenzylamino-1,1-bis(4-methoxyphenyl)-1-propanol (3.45 g).
Preparation 14 3-(Dibenzylamino)-1,1-bis(4-methoxyphenyl)-1-propanol (2.0 g) was hydrogenated by the usual manner to give N-benzyl-[3,3-bis(9-methoxyphenyl)propyl]amine, which was further hydrogenated by heating with 20o palladium on charcoal and ammonium formate in methanol to give [3,3-bis(4-methoxyphenyl)propyl]amine (165 g).
Preparation 15 To a solution of 4-benzyloxy-3-nitrophenyl acetate (4.20 g) in methanol (20 ml), 28o sodium methoxide-methanol solution (2.96 g) was added and evaporated. To the crude residue, N,N-dimethylformamide (20 ml) and (2S)-3-[(3-nitrophenyl)sulfonyloxy]-1,2-epoxypropane (3.80 g) were added. The mixture was stirred at room temperature overnight, and worked up in the usual manner to give (2S)-3-(4-benzyloxy-3-nitrophenoxy)-1,2-epoxypropane (4.30 g).
NMR (CDC13, ~): 2.72-2.77 (1H, m), 2.92 (1H, quintet, J=4.8Hz), 3.32-3.37 (1H, m), 3.91 (1H, quartet, J=5.9Hz), 4.27 (1H, dd, J=2.8 and 11.4Hz), 5.18 (2H, s), 7.07-7.15 (2H, m), 7.34-7.46 (6H, m) Preparation 16 A mixture of 3-(dibenzylamino)-1,1-bis(4-bromophenyl)-1-propanol (8.42 g), benzophenone imine (10.8 g), tris(dibenzylideneacetone)dipalladium (546 mg), (RS)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (l.ll g), sodium tert-butoxide (5.7 g) and toluene (90 ml) was stirred at 100°C for 6 hours. The reaction mixture was added to tetrahydrofuran (300 ml), and 3N hydrochloric acid (300 ml) and stirred at room temperature for 1.5 hours. The aqueous phase was separated, neutralized by sodium hydroxide and extracted with ethyl acetate. The ethyl acetate solution was evaporated and purified by silica gel column chromatography (hexane: ethyl acetate =1:1) to give 3-(dibenzylamino)-1,1-bis(4-aminophenyl)-1-propanol (1.76 g).
MS m/z: 438 (M++1) Preparation 17 The following compound was obtained according to a similar manner to that of Preparation 16.
(3RS)-3-(Dibenzylamino)-l,1-bis(4-aminophenyl)-1-butanol IR (Neat): 3356 (m), 3219 (m), 2964 (m),.1622 (s), 1512 (s), 1454 (m), 1383 (w), 1271 (m), 1246 (m), 1176 (m), 1142 (m), 831 (m) cm-1 NMR (CDC13, b): 1.03 (3H, d, J=6.7Hz), 2.02 (1H, d, J=11.7Hz), 2.50 (1H, dd, J=11.2 and 14.7Hz), 3.10-3.2 (1H, m), 3.21 (2H, d, J=13.OHz), 3.92 (2H, d, J=12.9Hz), 6.35 (2H, d, J=6.5Hz), 6.55 (2H, d, J=6.6Hz), 6.76 (2H, d, J=6.6Hz), 7.13 (2H, d, J=6.5Hz), 7.24 (lOH, s) MS m/z: 452 (M++1) Preparation 18 To a mixture of 3-(dibenzylamino)-1,1-bis(4-aminophenyl)-1-propanol (0.64 g), pyridine (0.5 ml) and dichloromethane (10 ml), methyl chlorocarbonate (0.34 ml) was added at 0°C and the reaction mixture was worked up in a usual manner. The crude product was dissolved in methanol (10 ml), followed by addition of 4N hydrogen chloride in 1,4-dioxane (0.5 m:L) and 20o palladium hydroxide on charcoal.
The mixture was stirred under hydrogen (1 atm) at room temperature overnight, worked up in a usual manner and purified by silica gel column chromatography (dichloromethane:methanol:concentrated ammonia water =

20:1:0.1) to give N-benzyl-[3,3-bis[4-[(methoxycarbonyl)-amino]phenyl]propyl]amine (466 mg).
MS m/z: 448 (M++1) Preparation 19 A mixture of (3RS)-3-aminobutyric acid methyl ester hydrochloride (5.0 g), benzyl bromide (11.7 g), potassium carbonate (18 g) and N,N-dimethylformamide (40 ml) was stirred at room temperature overnight, worked up in the usual manner and purified by silica gel column chromatography (hexane:ethyl acetate = 15:1) to give (3RS)-3-(dibenzylamino)butyric acid methyl ester (7.27 g).
IR (Neat): 2968 (m), 1741 (s), 1454 (m) 1259 (m), 1196 (m), 1146 (m), 1072 (m), 1022 (m), 744 (m), 698 (m) cm-1 NMR (CDC13, ~): 1.10 (3H, d, J=6.7Hz), 2.28 (1H, dd, J=6.9 and 13.9Hz), 2.64 (1H, dd, J=8.01 and 13.9Hz), 3.30 (1H, dd, J=6.8 and 14.7Hz), 3.49 (2H, d, J=13.7Hz), 3.60 (3H, s), 3.66 (2H, d, J=13.7Hz), 7.18-7.35 (10H, m) MS m/z: 298 (M++1) Preparation 20 The following compound was obtained according to a similar manner to that of Preparation 19.
(3RS)-3-[N-Benzyl-((2S)-2-hydroxy-3-phenoxypropyl)-amino]butyric acid methyl ester MS m/z: 358 (M++1) Preparation 21 To a mixture of (3RS)-3-(dibenzylamino)-l,l-bis(4-aminophenyl)-1-butanol (360 mg), triethylamine (0.44 ml) and dichloromethane (4 ml), methanesulfonyl chloride (0.20 ml) was added dropwise at 0°C. The reaction mixture was stirred at room temperature for 30 minutes and worked up in the usual manner. The crude product was dissolved in methanol followed by addition of loo palladium on charcoal (50o wet) and ammonium formate, heated under reflux for 1.5 hours, 5 filtrated and extracted by water. The aqueous solution was treated with benzyl chlorocarbonate (136 ~1) in the usual Shotten method, worked up in the usual manner and purified by silica gel column chromatography (hexane: ethyl acetate = 2:3) to give (3RS)-[3,3-bis[4-(methanesulfonylamino)phenyl]-1-10 methylpropyl]carbamic acid benzyl ester (138 mg).
IR (Neat): 3259(m), 1680 (s), 1512 (s), 1331 (m), 1153 (s) , 974 (m) cm-1 NMR (CDC13, d): 1.13 (3H, d, J=6.8Hz), 2.4-2.6 (2H, m), 2.98 (6H, s), 3.7-3.9 (1H, m), 4.6-4.8 (1H, m), 15 6.52 (2H, s), 7.07-7.15 (5H, m), 7.2-7.5 (8H, m) Preparation 22 (3RS)-1,1-Bis[4-(methanesulfonylamino)phenyl]-3-butylamine (77.4 mg) was obtained from (3RS)-[3,3-bis[4-20 (methanesulfonylamino)phenyl]-:L-methylpropyl]carbamic acid benzyl ester (1.01 mg) by hydrogenation in the usual manner.
IR (KBr): 3425 (br s), 1635 (m), 1506 (m), 1325 (m), 1151 (s), 1103 (m), 980 (w) cm-1 NMR (MeOH-d4, d): 1.13 (3H, d, J=6.4Hz), 2.05 (2H, 25 quartet, J=7.7Hz), 2.73 (1H, quartet, J=6.5Hz), 2.89 (6H, s), 4.06 (1H, dd, J=7.8Hz and 14.8Hz), 7.16 (4H, d, J=8.5Hz), 7.26 (9H, d, J=8.5Hz) MS m/z: 412 (M++1) 30 Preparation 23 To a mixture of (3RS)-3-(dibenzylamino)-l,l-bis(4-aminophenyl)-1--butanol (0.40 g), triethylamine (0.37 ml) and dichloromethane (4 ml), acetic anhydride (0.18 ml) was added at 0°C, followed by addition of additional triethylamine (0.1 ml) and acetic anhydride (0.09 ml). The reaction mixture was worked up in the usual manner to give (3RS)-3-(dibenzylamino)-1,1-bis[4-(acetylamino)phenyl]-1-butanol (0.49 g) .
IR (Neat): 2300 (m), 1666 (s), 1623 (m), 1539 (s), 1514 (m) , 1319 (m) , 1265 (m) , 1142 (w) , 837 (m) cm-1 NMR (CDC13, b): 1.06 (3H, d, J=6.6Hz), 2.12 (3H, s), 2.16 (3H, s), 2.0-2.2 (1H, m), 2.45-2.58 (1H, m), 3.0-3.2 (1H, m), 3.20 (2H, d, J=12.9Hz), 3.92 (2H, d, J=13.OHz), 6.72 (2H, d, J=6.8Hz), 7.09-7.36 (16H, m) MS m/z: 536 (M++1) Preparation 24 (3RS)-3-Amino-1,1-bis[4-(acetylamino)phenyl]-1-butanol (0.23 g) was obtained from (3RS)-3-(dibenzylamino)-1,1-bis[4-(acetylamino)phenyl]-1-butanol (0.32 g) by the usual hydrogenation.
IR (KBr): 3294 (m), 1666 (s), 1623 (s), 1537 (s), 1514 (m), 1406 (m), 1321 (n), 1014 (m) cm-1 NMR (MeOH-d6, b): 1.10-1.15 (3H, m), 2.07 (3H, s), 2.11 (3H, s), 2.5-3.1 (3H, m), 4.23 (2H, d, J=10.6Hz), 4.55 (2H, d, J=10.6Hz), 7.21-7.58 (8H, m) Preparation 25 The following compound was obtained according to a similar manner to that of Example 33.
(3RS)-3-(Dibenzylamino)-1,1-bis[4-(methoxycarbonyl-amino)phenyl]-1-butanol MS m/z: 568 Preparation 26 (3RS)-1,1-Bis[4-(methoxycarbonylamino)phenyl]-3-butylamine hydrochloride (191 mg) was obtained from (3RS)-3-(dibenzylamino)-l,l-bis(4-methoxycarbonylaminophenyl)butanol (173 mg) by hydrogenation in the usual manner.
MS m/z: 372 (M++1) (free) Preparation 27 Methanesulfonyl chloride (1.4 ml) was added dropwise to a solution of 3-amino-4-benzyloxyphenyl acetate (4.3 g) in pyridine (20 ml) under ice cooling over 10 minutes and the mixture was stirred at room temperature for a further 1 hour.
To the reaction mixture was added water (100 ml) and was stirred at the same temperature for 1 hour. The precipitates were collected by filtration and dissolved into chloroform (100 ml), followed by its dryness over magnesium sulfate and its evaporation in vacuo. The residue was chromatographed (hexane-ethyl acetate) over silica gel to afford 4-benzyloxy-3-(methanesulfonylamino)phenyl acetate (1.6 g).
NMR (CDC13, d): 2.27 (3H, s), 2.95 (3H, s), 5.09 (2H, s), 6.80-7.03 (3H, m), 7.25-7.95 (6H, m) MS m/z: 336 (M++1) _Preparation 28 A solution of 4-benzyloxy-3-(methanesulfonylamino)phenyl acetate (1.6 g) and potassium hydroxide (2.67 g) in methanol (10 ml) was stirred for 18 hours at room temperature. The reaction mixture was acidified with 1N hydrochloric acid to pH 5-7 and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was chromatographed (hexane-ethyl acetate) over silica gel to afford N-(2-benzyloxy-5-hydroxyphenyl)methanesulfonamide (750 mg).
NMR (CDC1 j, b) : 2.90 (3H, s) , 5.04 (2H, s) , 6.58 (1H, dd, J=2.9 arid 8.8Hz), 6.80-6.90 (2H, m), 7.09 (1H, d, J==2.9Hz), 7.30-7.50 (6H, m) MS m/z: 2 94 (M++1) Preparation 29 Under nitrogen, to a solution of N-(2-benzyloxy-5-hydroxyphenyl)methanesulfonamide (740 mg) and sodium hydride (92.4 mg) in N,N-dimethylformamide (30 ml) was added (2S)-glycidyl tosylate (616 mg) at 0°C and the mixture was stirred at the same temperature for 0.5 hour. The mixture was allowed to warm to room temperature and stirred for 2.5 hours at the same temperature. The resulting mixture was poured into 10% aqueous ammonium chloride solution, and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was chromatographed (hexane-ethyl acetate) over silica gel to afford (2S)-3-[4-benzyloxy-3-(methanesulfonamino)phenoxy]-1,2-epoxypropane (440 mg).
NMR (CDC13, ~): 2.75 (1H, dd, J=2.7 and 4.9Hz), 2.84-2.95 (4H, m), 3.30-3.37 (1H, m), 3.90 (1H, dd, J=5.8 and 11.08Hz), 4.07-4.25 (1H, m), 5.05 (2H, s ) , 6. 63-7 . 4 8 ( 9H, m) MS m/z: 350 (M++1) Preparation 30 Under nitrogen, a solution of N-benzyl-[3,3-bis(4-methoxyphenyl)-1-methylpropyl]amine (480 mg), N-[2-benzyloxy-5-[(1R)-2-iodo-1-(triethylsilyloxy)ethyl]phenyl]-methanesulfonamide (600 mg) and N,N-diisopropylethylamine (0.74 ml) in tetrahydrofuran (6 ml) was sealed with stirring at 110°C for 58 hours, followed by at 160°C for 92 hours.
The resulting mixture was poured into aqueous sodium hydrogen sulfite and extracted with ethyl acetate. The organic layer was washed successively with saturated aqueous sodium bicarbonate and brine, dried over anhydrous sodium sulfate, and evaporated in vacuo. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate = 10:1 to 5:1) to give N-[5-[(1R)-2-[N-benzyl-[(1RS)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]amino]-1-(triethylsilyloxy)-ethyl]-2-(benzyloxy)phenyl]methanesulfonamide (226 mg).

NMR (CDC13, b): 0.25-0.5 (6H, m), 0.7-0.95 (12H, m), 1.5-2.25 (2H, m), 2.35-2.9 (6H, m), 3.45-3.9 (8H, m), 4.25-4.4 (1H, m), 5.0-5.1 (2H, m), 6.65-7.75 (21H, m) Preparation 31 N-Benzyl-[(1S)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]-amine hydrochloride (800 mg) was dehydrochlorinated with saturated aqueous sodium bicarbonate and extracted with ethyl acetate. A mixture of the above obtained product and l00 palladium on activated carbon (50o wet, 300 mg) in methanol (10 ml) was stirred at room temperature in the presence of hydrogen at an atmospheric pressure for 5.5 hours. After filtration, the filtrate was evaporated in vacuo to give [(1S)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]amine (568 mg).
NMR (CDC13, ~): 1.10 (3H, d, J=6.3Hz), 1.95-2.1 (2H, m), 2.7-2.9 (1H, m), 3.76 (6H, m), 3.98 (1H, t, J=8.OHz), 6.75-6.9 (4H, m), 7.1-7.2 (4H, m) Preparation 32 The following compound was obtained according to a similar manner to that of Preparation 31.
[(1R)-3,3-Bis(4-methoxyphenyl)-1-methylpropyl]amine NMR (CDC13, b): 1.19 (3H, d, J=6.3Hz), 1.9-2.1 (2H, m), 2 . 7-2 . 85 ( 1H, m) , 3 . 76 ( 6H, m) , 3 . 98 ( 1H, t, J=7.9Hz), 6.75-6.9 (4H, m), 7.15 (4H, d, J=8.OHz) Preparation 33 A mixture of N-benzyl-[3,3-bis(4-hydroxyphenyl)-1-methylpropyl]amine (300 mg) and loo palladium on activated carbon (50o wet, 100 mg) in methanol (5 ml) was stirred at room temperature in the presence of hydrogen at an atmospheric pressure for 4 hours. After filtration, the filtrate was evaporated in vacuo to give [3,3-bis(4-hydroxyphenyl)-1-methylpropyl]amine (230 mg).
NMR (DMSO-d6, ~): 0.96 (3H, d, J=5.3Hz), 1.75-1.9 (2H, m), 2.4-2.6 (1H, m), 3.87 (1H, t, J=7.9Hz), 6.63 5 (4H, d, J=8.5Hz), 7.03 (4H, d, J=8.2Hz) Preparation 34 The following compound was obtained according to a similar manner to that of Preparation 33.
N-Benzyl-[3,3-bis(4-methoxyphenyl)-1-methylpropyl]amine Preparation 35 A mixture of 6-[(4-nitrophenyl)azo]pyridin-3-of (J. Am.
Chem. Soc. 1959, 81, 6049, 300 mg) and 20o palladium hydroxide on carbon (60 mg) in a mixture of acetic acid (30 ml) and methanol (30 ml) was stirred at room temperature in the presence of hydrogen at an atmospheric pressure for 70 minutes. After filtration, the filtrate was evaporated in vacuo. Under nitrogen, to a mixture of the residue in dichloromethane (10 ml) was added bis(trimethylsilyl)-acetamide (6.0 ml) at 5°C. After being stirred at room temperature for_ 30 minutes, to the resulting mixture was added benzyl chloroformate (0.54 ml) at 5°C, and the mixture was stirred at the same temperature for 3 hours. The resulting mixture was poured into saturated aqueous sodium bicarbonate, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. To the residue was added chloroform and insoluble materials were filtered off. After the filtrate was evaporated in vacuo, the residue was purified by column chromatography on silica gel (chloroform:methanol = 50:1 to 20:1), followed by crystallization from toluene-methanol to give (5-hydroxypyridin-2-yl)carbamic acid benzyl ester (159 mg).

MS m/z: 245 (M++1) Preparation 36 Under nitrogen, a suspension of sodium hydride (60% in oil, 189 mg) in N,N-dimethylformamide (20 ml) was dropwise added (5-hydroxypyridin-2-yl)carbamic acid benzyl ester (1.1 g) in N,N-dimethylformamide (12 ml) at 5°C, and the mixture was stirred at room temperature for 1 hour. To this one was added (2S)-glycidyl tosylate (1.1 g) at 5°C, and the mixture was stirred at room temperature for 7 hours. The resulting mixture was poured into saturated aqueous sodium bicarbonate, and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was purified by column chromatography on silica gel (chloroform: ethyl acetate = 9:1) to give (2S)-3-[2-(benzyloxycarbonylamino)pyridin-5-yloxy]-1,2-epoxypropane (780 mg).
MS m/z: 301 (M++1) Preparation 37 To a suspension of but-3-enylbenzene (3 ml) and sodium bicarbonate (2.5 g) in a mixture of dichloromethane (200 ml) and water (60 ml) was added small portions of m-chloroperbenzoic acid (3.5 g) at room temperature, and the mixture was stirred at the same temperature for 4 hours.
After separation, the organic layer was washed successively with saturated aqueous sodium bicarbonate and brine, dried over anhydrous magnesium sulfate and evaporated in vacuo.
The residue was purified by column chromatography on silica gel (hexane: ethyl acetate = 100:3) to give phenethyloxirane ( 970 mg) .
NMR (CDC13, b): 1.7-1.9 (2H, m), 2.45-2.5 (1H, m), 2.7-3.0 (4H, m), 7.1-7.4 (5H, m) Preparation 38 Under nitrogen, to a solution of (2R)-glycidyl tosylate (3.0 g) in tetrahydrofuran (30 ml) were added N,N-diisopropylethylamine (2.5 ml) and thiophenol (1.3 ml) at 5°C, and the mixture was stirred at room temperature for 12 hours. The resulting mixture was poured into water and extracted with ethyl acetate. The organic layer was washed successively with saturated aqueous sodium bicarbonate and brine, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (hexane: ethyl acetate = 5:1 to 3:1) to give toluene-4-sulfonic acid (2S)-2-hydroxy-3-(phenylthio)propyl ester (3.9 g) .
NMR (CDC13, ~): 2.44 (3H, m), 2.75-3.25 (3H, m), 3.85-4.3 (3H, m), 7.15-7.4 (7H, m), 7.7-7.8 (2H, m) Pr~ration 39 Under nitrogen, to a solution of toluene-4-sulfonic acid (2S)-2-hydroxy-3-(phenylthio)propyl ester (3.9 g) in ethanol (40 ml) was added 20o sodium methoxide in ethanol (4.7 ml) at 5°C, and the mixture was stirred at the same temperature for minutes. After being filtrated off to remove precipitates, the filtrate was concentrated in vacuo. The residue was dissolved into a mixture of aqueous O.1N sodium hydroxide and diethyl ether. After separation, the organic 25 layer was washed successively with water and brine, dried over anhydrous magnesium sulfate and evaporated in vacuo.
The residue was purified by column chromatography on silica gel (hexane:ethyl acetate = 20:1 to 10:1) to give (2S)-3-(phenylthio)-1,2-epoxypropane (1.5 g).
30 MS m/z: 167 (M++1) Example 6 To a solution of 4-bromothioanisole (508 mg) in tetrahydrofuran, butyllithium (1.54M in hexane, 1.62 ml) was added at -78°C. After 30 minutes, (3RS)-3-[((2S)-2-hydroxy-3-phenoxypropyl)amino]butyric acid methyl ester (131 mg) was added and warmed to 0°C. The reaction mixture was worked up in the usual manner and purified by a silica gel column chromatography to give (2S)-1-phenoxy-3-[(3RS)-1,1-bis[4-(methylthio)phenyl]-1-hydroxy-3-butyl]amino-3-propanol (58.5 mg).
IR (Neat): 3400 (br s), 2921 (s), 1594 (s), 1492 (s), 1243 (s), 1093 (m), 1043 (m), 817 (s), 754 (s) cm-1 NMR (CDC13, ~): 1.14 (3H, d, J=6.3Hz), 2.4-2.6 (2H, m), 2.43 (3H, s), 2.46 (3H, s), 2.7-2.8 (2H, m), 2.88 (1H, dd, J=11.9 and 8.OHz), 3.9-4.1 (3H, m), 6.9-7.0 (3H, m), 7.1-7.4 (12H, m) Example 7 The following compounds were obtained according to a similar manner to that. of Example 6.
(1) (2S)-1-Phenoxy-3-[(3RS)-1,1-bis(3-methoxyphenyl)-1-hydroxy-3-butyl]amino-2-propanol IR (Neat) : 3296 (br m) , 2933 (s) , 1599 (s) , 1491 (s) , 1464 (m), 1246 (s), 1171 (m), 1045 (s), 756 (m), 694 (m) cm-1 NMR (CDC13+D20, b): 1.09 (3H, d, J=6.3Hz), 2.04 (1H, dd, J=11.9 and 14.2Hz), 2.39-2.49 (2H, m), 2.6-2.8 (1H, m), 2.83 (1H, dd, J=8.3 and 11.9Hz), 3.74 (3H, s), 3.76 (3H, s), 3.8-3.9 (2H, m), 3.9-4.1 (1H, m), 6.72-6.75 (2H, m), 6.8-7.1 (7H, m), 7.12-7.31 (4H, m) MS m/z: 452 (M++1) (2) (2S)-1-Phenoxy-3-((3RS)-1,1-diphenyl-1-hydroxy-3-butyl)-amino-2-propanol IR (Neat): 3292 (br m), 2925 (m), 1597 (m), 1495 (s), 1456 (m) , 1244 (s) , 1043 (m) , 754 (s) , 698 (s) cm-1 MS m/z: 392 (M++1) (3) (2S)-1-Phenoxy-3-[(3RS)-1,1-bis(4-methoxyphenyl)-1-hydroxy-3-butyl]amino-2-propanol IR (Neat) : 3292 (br m) , 2929 (m) , 1604 (m) , 1508 (s) , 1460 (m), 1248 (s), 1176 (m), 1038 (m), 833 (m), 756 (m) cm-1 NMR (CDC13, ~): 1.12 (1.5H, d, J=5.lHz), 1.16 (1.5H, d, J=6.2Hz), 2.0-2.5 (2H, m), 2.6-3.2 (3H, m), 3.74 (1.5H, s) , 3.75 (1.5H, s) , 3.78 (3H, s) , 3.8-4.2 (3H, m), 6.77-7.01 (7H, m), 7.2-7.4 (6H, m) MS m/z: 452 (M++1) (4) (2S)-1-Phenoxy-3-[(3RS)-l,l-bis(3,4-dimethoxyphenyl)-1-hydroxy-3-butyl]amino-2-propanol IR (Neat) : 3294 (br m) , 2933 (m) , 1597 (w) , 1510 (s) , 1460 (m), 1257 (s), 1146 (m), 1028 (m), 760 (m) cm-l MS m/z: 512 (M++1) (5) (2S)-1-Phenoxy-3-[(3RS)-1,1-bis(4-methylphenyl)-1-hydroxy-3-butyl]amino-2-propanol IR (Neat): 3400 (br s), 2923 (s), 1596 (m), 1498 (s), 1457 (s) , 12.43 (s) , 1087 (m) , 1043 (m) , 817 (s) , 754 (s) cm 1 NMR (CDC13, ~): 1.13 (2H, d, J=6.2Hz), 2.16 (3H, s), 2.31 (3H, s), 2.4-2.5 (2H, m), 2.6-2.9 (3H, m), 3.9-4.1 (3H, m), 6.9-7.4 (13H, m) MS m/z: 420 (M++1) (6) 5-[N-Benzyl-((2S)-2-hydroxy-3-phenoxypropyl)amino]-1,1-bis(4-methoxyphenyl)-1-pentanol IR (Neat): 3446 (br m), 2943 (m), 1604 (m), 1508 (s), 1458 (m), 1248 (s), 1176 (m), 1036 (m), 831 (m), 752 (m) cm-1 NMR (CDC13, ~): 1.2-1.3 (2H, m), 1.4-1.7 (2H, m), 2.1-2.2 (2H, m), 2.4-2.7 (4H, m), 3.4-3.6 (1H, m), 3.78 (6H, s), 3.7-3.8 (1H, m), 3.8-3.9 (2H, m), 3.9-4.1 (1H, rn), 6.77-6.97 (7H, m), 7.2-7.4 (11H, m) MS m/z: 556 (M++1) 5 (7) 4-[N-Benzyl-((2S)-2-hydroxy-3-phenoxypropyl)amino]-1,1-bis(4-methoxyphenyl)-1-butanol IR (Neat): 3446 (br m), 2951 (m), 1604 (m), 1508 (s), 1458 (m), 1248 (s), 1176 (m), 1036 (s), 831 (m), 752 (m) cm-1 10 NMR (CDC13, ~): 1.5-1.7 (2H, m), 2.1-2.4 (2H, m), 2.4-2.7 (4H, m), 3.4-3.5 (1H, m), 3.77 (6H, s), 3.7-3.8 (1H, m), 3.8-4.0 (2H, m), 4.1-4.3 (1H, m), 6.78-6.98 (7H, m), 7.2-7.4 (11H, m) MS m/z: 542 (M++1) (8) (2S)-1-Phenoxy-3-[(1RS)-3,3-bis(4-methoxyphenyl)-3-hydroxy-1-(3,4-dimethoxyphenyl)propyl]amino-2-propanol IR (Neat): 3361 (br m), 2929 (m), 1602 (m), 1512 (s), 1459 (m), 1298 (s), 1032 (s), 833 (m), 756 (m) cm-1 NMR (CDC13, b): 2.3-2.8 (5H, m), 3.74 (3H, s), 3.82 (3H, s), 3.86 (6H, s), 3.9-4.1 (3H, m), 6.6-7.1 (8H, m), 7.2-7.5 (8H, m) MS m/z: 574 (M++1) (9) (2S)-1-Phenoxy-3-[(1RS)-3,3-bis(4-methoxyphenyl)-3-hydroxy-1-phenylpropyl]amino-2-propanol IR (Neat): 3361 (br m), 2929 (m), 1603 (m), 1506 (s), 1458 (m), 1296 (s), 1176 (m), 1035 (m), 833 (m), 756(m), 698 (m) cm-1 NMR (CDC13, ~): 2.3-2.8 (4H, m), 3.6-3.7 (1H, m), 3.74 ( 3H, s ) , 3 . 82 ( 3H, s ) , 3 . 8-4 . 2 ( 4H, m) , 6 . 7-7 . 0 (9H, m), 7.1-7.2 (2H, m), 7.2-7.4 (5H, m), 7.4-7.5 (2H, m) MS m/z: 514 (M++1) (10) (2S)-1-Phenoxy-3-[3,3-bis(4-methoxyphenyl)-3-hydroxyphenyl]amino-2-propanol IR (Neat): 3313 (br m), 2931 (m), 1602 (s), 1508 (s), 1462 (m), 1248 (s), 1176 (m), 1036 (m), 831 (m), 756 (m) cm-1 NMR (CDC13+D20, b): 2.3-2.5 (2H, m), 2.7-2.9 (4H, m), 3.77 (6H, s), 3.9-4.2 (4H, m), 6.80-7.01 (7H, m), 7 . 2-7 . 4 ( 6H, m) MS m/z: 938 (M++1) Example 8 The following compounds were obtained according to a similar manner to that of Preparation 33.
(1) (2S)-1-Phenoxy-3-[5,5-bis(4-methoxyphenyl)pentyl)-amino-2-propanol hydrochloride IR (Neat) : 3322 (br m) , 1602 (m) , 1510 (s) , 1460 (m) , 1246 (s), 1178 (m), 1036 (m), 831 (m) cm-1 NMR (MeOH-d4, ~): 1.2-1.4 (2H, m), 1.6-1.8 (2H, m), 2.04 (2H, quartet, J=7.5Hz), 2.99 (2H, t, J=8.OHz), 3.09-3.22 (2H, m), 3.73 (6H, s), 3.6-3.85 (1H, m), 3.9-4.0 (2H, m), 4.1-4.3 (1H, m), 6.84 (4H, d, J=8.7Hz), 6.9-7.0 (3H, m), 7.14 (4H, d, J=8.6Hz), 7.28 (2H, t, J=7.9Hz) MS m/z: 450 (M++1) (free) (2) (2S)-1-Phenoxy-3-[4,4-bis(4-methoxyphenyl)butyl]amino-2-propanol hydrochloride IR (Neat): 3355 (br m), 1602 (m), 1510 (s), 1960 (m), 1246 (s) 1178 (m), 1036 (m), 831 (m) cm-1 NMR (MeOH-d4, b): 1.6-1.8 (2H, m), 2.08 (1H, quartet, J=7.9Hz), 2.55 (1H, quartet, J=7.6Hz), 3.0-3.2 (4H, m) , 3. 73 ( 6H, s) , 3. 7-4 . 3 (4H, m) , 6. 8-7 . 0 (7H, m) , 7.1-7.4 (6H, m) MS m/z: 436 (M++1) (free) Example 9 A mixture of (2S)-1-phenoxy-3-[(3RS)-1,1-bis[4-(methylthio)phenyl]-1-hydroxy-3-butyl]amino-2-propanol (47 mg), water (2 ml), methanol (3 ml) and OXONE~ (potassium peroxymonosulfate) (180 mg) was stirred at room temperature overnight and worked up in the usual manner to give (2S)-1-phenoxy-3-[(3RS)-1,1-bis(4-methanesulfonylphenyl)-1-hydroxy-3-butyl]amino-2-propanol (52 mg).
IR (Neat): 3521 (br m), 2927 (m), 1595 (m), 1494 (s), 1309 (s), 1244 (m), 1149 (s), 1091 (m), 958 (m), 771 (s), 694 (m) cm-1 NMR (CDC13, d): 1.19 (3H, d, J=6.3Hz), 2.3-2.8 (4H, m), 2.9 (1H, m), 3.00 (3H, s), 3.05 (3H, s), 3.9-4.1 (3H, m), 6.9-7.1 (3H, m), 7.2-7.4 (1H, m), 7.5-7.74 (5H, m), 7.8-7.9 (4H, m) MS m/z: 548 (M++1) Example 10 A mixture of (2S)-3-phenoxy-1,2-epoxypropane (40 mg), 3-amino-3-(3,4-dimethoxyphenyl)propionic acid methyl ester acetate (80 mg), triethylamine (0.5 ml) and methanol (3 ml) was heated under reflux, evaporated and purified by silica gel column chromatography (hexane:ethyl acetate:methanol =
1:1:0.07) to give (3RS)-3-((2S)-2-hydroxy-3-phenoxypropyl)-amino-3-(3,4-dimethoxyphenyl)propionic acid methyl ester (92 mg ) .
IR (Neat): 2925 (m), 1738 (s), 1597 (m), 1514 (s), 1460 (m), 1263 (m), 1138 (m), 1027 (s), 758 (m) cm-1 NMR (CDC13, ~): 2.6-2.8 (4H, m), 3.67 (3H, s), 3.87 (6H, s), 3.9-4.0 (2H, m), 4.0-4.1 (2H, m), 6.8-7.0 (7H, m), 7.26 (1H, t, J=8.9Hz) MS m/z: 390 (M++1) Example 11 The following compound was obtained according to a similar manner to that of Example 10.
(2S)-1-Phenoxy-3-[1,1-bis(4-methoxyphenyl)-3-methyl-3-butyl]amino-2-propanol IR (Neat): 3350 (br m), 2962 (m), 1606 (m), 1508 (s), 1460 (m), 1248 (s), 1178 (m), 1036 (m), 829 (m), 756(m) cm-1 NMR (CDC13, 0 :1.03 (3H, s), 1.05 (3H, s), 2.22 (2H, d, J=6.8Hz), 2.55 (1H, dd, J=7.0 and 11.7Hz), 2.68 (1H, dd, J=3.6 and 11.7Hz), 3.73 (6H, s), 3.8-3.9 (3H, m) , 4.04 (1H, t, J=6.7Hz) , 6.7.7-6. 99 (7H, m) , 7.1-7.4 (6H, m) MS m/z: 450 (M++1) Example 12 A mixture of (2S)-3-phenoxy-1,2-epoxypropane (0.12 g), 1-[2,2-bis(4-methoxyphenyl)ethyl]cyclopentylamine (0.24 g) and methanol (5 ml) was heated under reflux, evaporated and purified by silica gel column chromatography (hexane: ethyl acetate:methanol = 1:1:0.07) to give N-((2S)-2-hydroxy-3-phenoxypropyl)-[1-[2,2-bis(4-methoxyphenyl)ethyl]-cyclopentyl]amine (40.9 mg).
IR (Neat): 2954 (m), 1606 (w), 1510 (s), 1460 (m), 1246 (m), 1176 (m), 1038(s), 825 (m), 754 (m) cm-1 NMR (CDC13, b): 1.2-1.8 (8H, m), 2.25 (2H, t, J=6.8Hz), 2.46 (1H, dd, J=6.9 and 12.OHz), 2.61 (1H, dd, J=4.4 and 12.OHz), 3.73 (6H, s), 3.8-3.9 (2H, m), 4.0-4.1 (2H, m), 6.78 (4H, d, J=8.2Hz), 6.9-7.0 (3H, m), 7.19 (4H, d, J=8.7Hz), 7.24-7.33 (2H, m) MS m/z: 476 (M++1) _Example 13 The following compounds were obtained according to a similar manner to that of Example 12.

(1) (1R)-1-(3-Pyridyl)-2-[[(3RS)-1,1-bis(4-methoxyphenyl)-3-butyl]amino]ethanol MS m/z: 407 (M++1) (2) (2S)-1-(3-Pyridyloxy)-3-[(3RS)-1,1-bis(4-methoxyphenyl)-3-butyl]amino-2-propanol dihydrochloride MS m/z: 437 (M++1) (free) (3) (2S)-1-(1H-Indol-4-yloxy)-3-[3,3-bis(4-methoxyphenyl)-propyl]amino-2-propanol MS m/z: 461 (M++1) (4) (2RS)-1-(2-Oxo-2,3-dihydro-1H-benzimidazol-4-yloxy)-3-[(3RS)-1,1-bis(4-methoxyphenyl)-3-butyl]amino-2-propanol MS m/z: 492 (M++1) (5) (2R)-3-[4-Benzyloxy-3-(methanesulfonylamino)phenyl]-1-[(3RS)-1,1-bis(4-methoxyphenyl)-3-butyl]amino-2-propanol (6) (2S)-1-Phenoxy-3-[(3RS)-l,l-bis[4-(methanesulfonyl-amino)phenyl]-3-butyl]amino-2-propanol IR (KBr): 3440 (br s), 1603 (m), 1508 (m), 1325 (m), 1242 (m) , 1151 (s) , 1103 (m) , 974 (m) , 758 (m) cm-1 NMR (CDC13, ~): 1.11 (3H, d, J=6.2Hz), 2.0-2.2 (2H, m), 2.2-2.9 (3H, m), 2.97 (6H, s), 3.9-4.0 (3H, br s), 4.1-4.2 (1H, m), 6.88-7.00 (4H, m), 7.10-7.33 (9H, m) MS m/z: 562 (M++1) (7) (2S)-1-Phenoxy-3-[(3RS)-1,1-bis[4-(acetylamino)phenyl)-1-hydroxy-3-butyl]amino-2-propanol MS m/z: 506 (M++1) (8) (2S)-1-Phenoxy-3-[(3RS)-1,1-bis[4-(acetylamino)phenyl]-3-butyl]amino-2-propanol MS m/z: 490 (M++1) Example 14 A mixture of (1S)-1-phenoxy-3-[3,3-bis(4-methoxyphenyl)-5 3-hydroxypropyl]amino-2-propanol (93 mg), p-toluenesulfonic acid hydrate (53 mg) and toluene was heated under reflux for 1.5 hours, evaporated and purified (preparative TLC, silica gel, loo methanol-dichloromethane) to give (1S)-1-phenoxy-3-[3,3-bis(4-methoxyphenyl)-2-propenyl]amino-2-propanol (80.5 10 mg).
IR (Neat): 3359 (br m), 1604 (s), 1510 (s), 1460 (m), 1248 (s), 1176 (m), 1034 (m), 835 (m), 756 (m), 686 (m) cm-1 NMR (CDC13+D20, b): 2.9-3.1 (2H, m), 3.58 (2H, d, 15 J=7.OHz), 3.77 (3H, s), 3.82 (3H, s), 3.9-4.0 (2H, m), 9.2-4.3 (1H, m), 6.07 (1H, t, J=7.lHz), 6.73-7.29 (13H, m) Example 15 20 To a mixture of (2S)-1-phenoxy-3-[3,3-bis(4-methoxyphenyl)-3-hydroxypropyl]amino-2-propanol (34 mg), triethylsilane (0.5 ml) and dichloromethane (1 ml), trifluoroacetic acid (0.1 ml) was added dropwise at room temperature. The reaction mixture was worked up immediately 25 in the usual manner and purified by silica gel preparative TLC (eluent; lOs methanol/dichloromethane) to give (2S)-1-phenoxy-3-[3,3-bis(4-methoxyphenyl)propyl]amino-2-propanol trifluoroacetat.e (21 mg).
IR (Neat): 3900 (br m), 2933 (m), 1680 (s), 1604 (m), 30 1508 (s), 1248 (s), 1203 (m), 1180 (s), 1134 (m), 1036 (m), 829 (m), 756 (m) cm-l NMR (CDC13, ~): 2.3-2.5 (2H, m), 2.7-2.9 (2H, m), 2.9-3.1 (2H, m), 3.74 (6H, s), 3.8-4.0 (3H, m), 4.1-4.3 (1H, m), 6.7-6.9 (6H, m), 6.95 (2H, t, J=7.9Hz), 35 7.10 (4H, d, J=8.5Hz), 7.26 (1H, t, J=7.9Hz) MS m/z: 422 (M++1) Example 16 A mixture of (2S)-3-phenoxy-1,2-epoxypropane (0.11 g), D-alanine bis(4-methoxyphenyl)methylamide (0.25 g) and methanol (4 ml) was heated under reflux overnight, evaporated and purified by silica gel column chromatography to give N-((2S)-2-hydroxy-3-phenoxypropyl)-D-alanine [bis(4-methoxyphenyl)methyl]amide (217 mg).
IR (KBr): 3290 (s), 1643 (s), 1606 (m), 1512 (s), 1642 (m), 1250 (s), 1176 (m), 1034 (s), 831 (w), 812 (m) , 752 (m) cm-1 NMR (CDC13, ~): 1.27 (3H, d, J=7.2Hz), 2.66 (1H, dd, J=3.8 and 12.OHz), 2.80 (1H, dd, J=7.6 and 12.OHz), 3.24 (1H, quartet, J=6.9Hz), 3.74 (3H, s), 3.78 (3H, s), 3.8-4.0 (3H, m), 6.14 (1H, d, J=8.6Hz), 6.8-6.9 (6H, m), 6.98 (1H, t, J=7.3Hz), 7.13 (4H, dd, J=2.0 and 8.6Hz), 7.29 (2H, t, J=7.4Hz), 7.71 (1H, d, J=8.6Hz) MS m/z: 465 (M++1) Example 17 To a suspension of lithium aluminum hydride (10 mg) in tetrahydrofuran (0.5 ml), a solution of N-((2S)-2-hydroxy-3-phenoxypropyl)-D-alanine [bis(4-methoxyphenyl)methyl]amide (52.4 mg) in tetrahydrofuran was added dropwise at 0°C under a flow of nitrogen. The reaction mixture was heated under reflux. After 2 hours, additional lithium aluminum hydride (50 mg) was added to the reaction mixture under a flow of nitrogen at 0°C. The reaction mixture was heated under reflux for 2.5 hours, worked up in the usual manner and purified (preparative TLC, 10% methanol-ethyl acetate) to give (2S)-1-phenoxy-3-[(2R)-1-[[bis(4-methoxyphenyl)methyl]-amino]-2-propyl]amino-2-propanol (31.4 mg).
IR (Neat): 3316 (br s), 2931 (m), 1606 (m), 1508 (s), 1458 (m), 1292 (s), 1174 (m), 1036 (s), 820 (m), 756 (m) cm-1 NMR (CDC13, d): 1.06 (3H, d, J=6.3Hz), 2.46 (1H, dd, J=8.7 and 12.OHz), 2.62 (1H, dd, J=9.2 and 12.OHz), 2. 80 (2H, d, J=4.7Hz) , 3.76 (6H, s) , 3. 9-4. 1 (3H, m), 4.71 (1H, s), 6.82 (4H, dd, J=2.0 and 6.7Hz), 6.9-7.0 (3H, m), 7.2-7.3 (6H, m) MS m/z: 451 (M++1) Example 18 A mixture of (2R)-2-[9-benzyloxy-3-(methanesulfonylamino)phenyl]-2-(triethylsilyloxy)-1-iodoethane (156 mg), [3,3-bis(4-methoxyphenyl)propyl]amine (75 mg), N,N-diisopropylethylamine (0.19 ml) and dimethylacetamide (0.75 ml) was heated at 110°C overnight and worked up in the usual manner. The crude product was treated with 4N hydrogen chloride in ethyl acetate (2 ml), worked up in the usual manner and purified by preparative TLC (10%
methanol-dichloromethane) to give (1R)-1-[4-benzyloxy-3-(methanesulfonylamino)phenyl]-2-[3,3-bis(4-methoxyphenyl)-propyl]aminoethanol (47 mg).
IR (Neat): 3310 (br m), 1608 (w), 1510 (s), 1460 (m), 1329 (m), 1248 (s), 1157 (s), 1120 (s); 1034 (m), 818 (m), 739 (m) cm-1 NMR (CDC13, b): 2.16 (2H, quartet, J=7.lHz), 2.5-2.7 (3H, m), 2.81 (1H, dd, J=3.6 and 12.2Hz), 2.90 (3H, s), 3.79 (6H, s), 3.95 (1H, t, J=7.9Hz), 4.55 (1H, dd, J=3.5 and 8.9Hz), 5.09 (2H, s), 6.81 (4H, d, J=8.6Hz), 6.95 (1H, d, J=8.5Hz), 7.13 (5H, d, J=8.6Hz), 7.35 (5H, s), 7.47 (1H, d, J=2.OHz) MS m/z: 591 (M++1) Example 19 The following compound was obtained according to a similar manner to that of Example 18.

(1R)-1-[4-Benzyloxy-3-(methanesulfonylamino)phenyl]-2-[[(3RS)-1,1-bis[4-(methoxycarbonylamino)phenyl]-3-butyl]-amino]ethanol Example 20 (1R)-1-[4-Benzyloxy-3-(methanesulfonylamino)phenyl]-2-[[3,3-bis(4-methoxyphenyl)propyl]amino]ethanol (35 mg) was hydrogenated by the usual manner to give (1R)-1-[4-hydroxy-3-(methanesulfonylamino)phenyl]-2-[[3,3-bis(4-methoxyphenyl)-propyl]amino]ethanol (19.3 mg).
IR (KBr): 3430 (br m), 1608 (w), 1510 (s), 1319 (m), 1304 (m) , 1248 (s) , 1.153 (m) , 1034 (m) , 825 (m) cm-1 NMR (CDC13, d): 2.1-2.3 (2H, m), 2.5-2.7 (2H, m), 2.7-2.9 (2H, m), 2.90 (3H, s), 3.74 (6H, s), 3.83 (1H, t, J=7.8Hz), 4.5-4.7 (1H, m), 6.79 (5H, d, J=8.3Hz), 7.01 (1H, d, J=8.lHz), 7.13 (4H, d, J=8.4Hz), 7.13 (1H, br s) MS m/z: 501 (M++1) Example 21 A mixture of (2S)-3-(4-benzyloxy-3-nitrophenoxy)-1,2-epoxypropane (197 mg), N-benzyl-[3,3-bis(4-methoxyphenyl)-propyl]amine (236 mg) and ethanol (3 ml) was heated under reflex for 12 hours. Iron powder, ammonium chloride and water were added to the reaction mixture and heating was continued for 1. hour. The reaction mixture was filtrated and worked up in the usual manner to give (2S)-1-(3-amino-9-benzyloxyphenoxy)-3-[N-benzyl-[3,3-bis(4-methoxyphenyl)-propyl]amino]-2-propanol (412.'7 mg).
NMR (CDC13, ~): 2.1-2.3 (2H, m), 2.4-2.7 (4H, m), 3.50 (1H, d, J=l4Hz), 3.75 (6H, s), 3.7-4.0 (5H, m), 5.01 (2H, s), 6.15-6.4 (2H, m), 6.71-6.80 (5H, m), 7.03-7.08 (4H, m), 7.2-7.4 (10H, m) MS m/z: 633 (M+~-1) Example 22 The following compounds were obtained according to a similar manner to that of Example 21.
(1) (2S)-1-(3-Amino-4-benzyloxyphenoxy)-3-[N-benzyl-[4,4-bis(4-methoxyphenyl)butyl]amino]-2-propanol NMR (CDC13, ~): 1.45 (2H, quintet, J=7.5Hz), 1.93 (2H, quintet), 2.3-2.6 (4H, m), 3.44 (1H, d, J=13.5Hz), 3.69-9.1 (4H, m), 3.76 (6H, s), 5.00 (2H, s), 6.17 (1H, dd, J=2.9 and 8.8Hz), 6.31 (1H, d, J=2.8Hz), 6.73 (1H, d, J=8.8Hz), 6.79 (4H, d, J=8.7Hz), 7.07 (4H, d, J=7.7Hz), 7.2-7.4 (lOH, m) MS m/z: 647 (M++1) (2) (1RS)-1-(3-Amino-4-benzyloxyphenyl)-2-[N-benzyl-[4,9-bis(4-methoxyphenyl)butyl]amino]ethanol NMR (CDC13, ~): 1.4-1.6 (2H, m), 1.8-2.1 (2H, m), 2.4-2.7 (4H, m) , 3.41 (1H, d, J=13. 5Hz) , 3.76 (6H, s ) , 3 . 7-3 . 9 ( 2H, m) , 4 . 51 ( 1H, t ) , 5 . 05 ( 2H, s ) , 6.50-6.65 (2H, m), 6.75-6.85 (5H, m), 7.05-7.15 (4H, m), 7.2-7.5 (lOH, m) MS m/z: 617 (M++1) (3) (2S)-1-Phenoxy-3-[[3,3-bis(4-ethoxyphenyl)propyl]-amino]-2-propanol IR (Neat): 3305 (br m), 1604 (m), 1510 (s), 1392 (w), 1300 (w), 1246 (s), 1176 (m), 1047 (s), 822 (m), 756 (m) cm-1 NMR (MeOH-d6, b): 1.34 (6H, t, J=7.OHz), 2.2-2.4 (2H, m), 2.6-2.9 (4H, m), 3.97 (4H, quartet, J=7.OHz), 3. 9-4. 1 (4H, m) , 6. 80 (4H, d, J=8. 6Hz) , 6. 89-7. 0 (3H, m), 7.14 (4H, d, J=8.6Hz), 7.26 (2H, t, J=7.9Hz) MS m/z: 450 (M++1) Example 23 To a mixture of (2S)-1-(3-amino-4-benzyloxyphenoxy)-3-[N-benzyl-[3,3-bis(4-methoxyphenyl)propyl]amino]-2-propanol (59 mg), pyridine (0.1 ml) and dichloromethane (1 ml), 5 methanesulfonyl chloride (27 ~1) were added at 0°C and stirred for 30 minutes. The reaction mixture was worked up in the usual manner. The crude product was hydrogenated in the usual manner to give (2S)-1-[4-hydroxy-3-(methanesulfonylamino)phenoxy]-3-[[3,3-bis(4-methoxyphenyl)-10 propyl]amino]-2-propanol (17.2 mg).
IR (KBr): 3440 (br s), 1610 (w), 1510 (s), 1460 (m), 1325 (m), 1248 (s), 1176 (m), 1151 (m), 1115 (w), 1034 (m), 816 (m) cm-1 NMR (MeOH-d4, d): 2.1-2.3 (2H, m), 2.5-2.8 (4H, m), 15 2. 91 (3H, s) , 3.74 (6H, s) , 3.8-4.1 (4H, m) , 6.6-6 . 7 ( 1H, m) , 6 . 7-6 . 9 ( 5H, m) , 6 . 97 ( 1H, d, J=2.7Hz), 7.1-7.2 (9H, m) MS m/z: 531 (M++1) 20 Example 24 The following compounds were obtained according to a similar manner to that of Example 23.
(1) (1R)-1-[4-Hydroxy-3-(methanesulfonylamino)phenyl]-2-25 [[3,3-bis[4-[(methoxycarbonyl)amino]phenyl]propyl]-amino]ethanol MS m/z: 587 (M++1) (2) (2S)-1-[(4-Hydroxy-3-(methanesulfonylamino)phenoxy]-3-30 [[3,3-bis[4-[(methoxycarbonyl)amino]phenyl]propyl]-amino]-2-propanol MS m/z: 617 (M++1) (3) (2S)-1-[4-Hydroxy-3-(methanesulfonylamino)phenoxy]-3-35 [4,4-bis(4-methoxyphenyl)butyl]amino-2-propanol IR (KBr) : 3480 (br m) , 1612 (m) , 1512 (s) , 1460 (m) , 1321 (w), 1248 (s), 1178 (m), 1113 (m), 1039 (m), 826 (m) cm-1 NMR (MeOH-d4, b): 1.4-1.6 (2H, m), 1.9-2.1 (2H, m), 2.6-2.8 (4H, m), 2.89 (3H, s), 3.73 (6H, s), 3.8-4.1 (4H, m), 6.61 (1H, dd, J=2.9 and 8.8Hz), 6.76 ( 1H, d, J=8 . 5Hz ) , 6 . 80 ( 4H, d, J=8 . 6Hz ) , 6 . 96 ( 1H, d, J=2.9Hz), 7.13 (4H, d, J=8.6Hz) MS m/z: 545 (M++1) (4) (1RS)-1-[4-Hydroxy-3-(methanesulfonylamino)phenyl]-2-[[4,4-bis(4-methoxyphenyl}butyl]amino]ethanol IR (KBr): 3420 (br m), 1560 (m), 1512 (s), 1321 (m), 1248 (s), 1153 (m), 1113 (w), 1039 (m), 817(m) cm-1 NMR (MeOH-d4, b): 1.4-1.7 (2H, m), 1.9-2.1 (2H, m), 2.7-2.9 (4H, m), 2.90 (3H, s), 3.73 (6H, s), 3.7-3.9 (1H, m), 4.6-4.8 (1H, m), 6.81 (4H, d, J=8.7Hz), 6.85 (1H, m), 7.05 (1H, m), 7.14 (4H, d, J=8.6Hz), 7.34 (1H, s) MS m/z: 515 (M++1) Example 25 To a solution of (2S)-1-phenoxy-3-[N-benzyl-[3,3-bis(4-methoxyphenyl)propyl]amino]-2-propanol (97 mg) and dichloromethane (1 ml), 1M boron tribromide-dichloromethane solution (0.28 ml) was added at -78°C. The reaction mixture was stirred at 0°C for 50 minutes and worked up in the usual manner to give (2S)-1-phenoxy-3-[N-benzyl-[3,3-bis(4-hydroxyphenyl)propyl]amino]-2-propanol (44 mg).
MS m/z: 484 (M++1) Example 26 To a mixture of (2S)-1-phenoxy-3-[N-benzyl-[3,3-bis(4-hydroxyphenyl)propyl]amino]-2-propanol (40 mg), N,N-diisopropylethylamine (43 ~l) and dichloromethane (1 ml), trifluoromethanesulfonic anhydride (31 ~1) was added at -78°C. The reaction mixture was worked up in the usual manner. A mixture of the obtained crude product, palladium acetate (5.6 mg), 1,3-bis(diphenylphosphino)propane (10.2 mg), triethylamine (46 ~,1), N,N-dimethylformamide (1 ml) and methanol (0.5 ml) was stirred at 100°C under carbon monoxide atmosphere (1 atm) for 3.5 hours, worked up in the usual manner and purified by preparative TLC (hexane: ethyl acetate - 3:1) to give (2S)-1-phenoxy-3-(N-benzyl-[3,3-bis[4-(methoxycarbonyl)phenyl]propyl]amino]-2-propanol (21 mg).
MS m/z: 568 (M++1) Example 27 N-[5-[(2S)-3-[N-Benzyl-[(1RS)-3,3-bis(4-hydroxyphenyl)-1-methylpropyl]amino]-2-hydroxypropoxy]-2-benzyloxyphenyl]-methanesulfonamide (120 mg) and 10o palladium on activated carbon (50% wet, 30 mg) in methanol (10 ml) was stirred at room temperature in the presence of hydrogen at an atmospheric pressure for 3 hours, and filtered. The filtrate was evaporated in vacuo and treated with 4N hydrogen chloride in ethyl acetate to afford N-[5-[(2S)-3-[[(1RS)-3,3-bis(4-hydroxyphenyl)-1-methylpropyl]amino]-2-hydroxypropoxy]-2-hydroxyphenyl]methanesulfonamide hydrochloride (50 mg).
MS m/z: 516 (M++1) (free) Example 28 The following compound was obtained according to a similar manner to that of Example 27.
N-[5-[(2S)-3-[[(1RS)-3,3-Bis(9-methoxyphenyl)-1-methylpropyl]amino]-2-hydroxypropoxy]-2--hydroxyphenyl]-methanesulfonamide hydrochloride MS m/z: 544 (M++1) (free) Example 29 (2S)-1-Phenoxy-3-[N-benzyl-[3,3-bis[4-(methoxycarbonyl)-phenyl]propyl]amino]-2-propanol (14 mg) was treated with sodium hydroxide in the usual manner and hydrogenated in the usual manner to give (2S)-1-phenoxy-3-[3,3-bis(4-carboxyphenyl)propyl]amino-2-propanol (12 mg).
MS m/z: 450 (M++1) Example 30 A mixture of (2S)-3-phenoxy-1,2-epoxypropane (0.36 g), N-benzyl-[3,3-bis[4-[(methoxycarbonyl)amino]phenyl]propyl]-amine (0.97 g) and ethanol (10 ml) was heated under reflux for 12 hours and cooled to room temperature. To the reaction mixture, loo palladium on charcoal (50o wet, 0.4 g), 4N
hydrogen chloride in 1,4-dioxane (1.1 ml) and methanol (5 ml) was added. The mixture was stirred under hydrogen (1 atm) for 3.5 hours, filtrated, diluted with ethyl acetate, neutralized by washing with aqueous sodium bicarbonate solution and the organic layer was evaporated. The crude product was purified by silica gel column chromatography(dichloromethane:methanol:concentrated ammonia water = 20:1:0.05) to give (2S)-1-phenoxy-3-[[3,3-bis[4-[(methoxycarbonyl)amino]phenyl]propyl]amino]-2-propanol, which was converted to the corresponding hydrochloride salt (0.71 g) in a usual manner.
IR (KBr): 3400 (br m), 1711 (s), 1599 (m), 1537 (s), 1317 (m), 1238 (s), 1072 (m), 758 (m) cm-1 NMR (MeOH-d4, ~): 2.3-2.5 (2H, m), 2.9-3.3 (4H, m), 3 . 65 ( 3H, s ) , 3 . 71 ( 3H, s ) , 3 . 9-4 . 00 ( 3H, m) , 4 . 1 4 . 3 ( 1H, m) , 6. 91-6. 98 ( 3H, m) , 7 . 18-7 . 39 ( lOH, m) MS m/z: 508 (M++1) (free) Example 31 The following compound was obtained according to a similar manner to that of Example 30.

(2S)-1-(4-Hydroxyphenoxy)-3-[(3RS)-1,1-bis(4-methoxyphenyl)-3-butyl]amino-2-propanol MS m/z: 452 (M++1) Example 32 The following compound was obtained according to a similar manner to that of Preparation 16.
(2S)-1-Phenoxy-3-[N-benzyl-[(3RS)-1,1-bis(4-aminophenyl)-1-hydroxy-3-butyl]amino]-2-propanol MS m/z: 512 (M++1) Example 33 To a mixture of (2S)-1-phenoxy-3-[N-benzyl-[(3RS)-1,1-bis(4-aminophenyl)-1-hydroxy-3-butyl]amino]-2-propanol (100 mg), pyridine (48 ~1) and dichloromethane (2 ml), methyl chlorocarbonate (33 ~l) was added at 0°C. The reaction mixture was worked up in the usual manner to give (2S)-1-phenoxy-3-[N-benzyl-[(3RS)-1,1-bis[4-[(methoxycarbonyl)-amino]phenyl]-1-hydroxy-3-butyl]amino]-2-propanol (125 mg).
MS m/z: 628 (M++1) Example 34 The following compound was obtained according to a similar manner to that of Example 33.
(2S)-1-Phenoxy-3-[N-benzyl-[(3RS)-1.,1-bis[4-[N-methyl-(methoxycarbonyl)amino]phenyl]-1-hydroxy-3-butyl]amino]-2-propanol MS m/z: 656 (M++1) Example 35 (2S)-1-Phenoxy-3-[N-(benzyl-[(3RS)-1,1-bis[4-[(methoxycarbonyl)amino]phenyl]-1-hydroxy-3-butyl]amino]-2-propanol (99 mg) was hydrogenated in the usual manner to give (2S)-1-phenoxy-3-[(3RS)-1,1-bis[4-[(methoxycarbonyl)amino]-phenyl]-3-butyl]amino-2-propanol (58 mg).
MS m/z: 522 (M++1) 5 Example 36 The following compounds were obtained according to a similar manner to that of Preparation 18.
(1) (2S)-1-Phenoxy-3-[(3RS)-l,l-bis[9-[(ethoxycarbonyl)-10 amino]phenyl]-3-butyl]amino-2-propanol hydrochloride MS m/z: 550 (M++1) (free) (2) (2S)-1-Phenoxy-3-[(3RS)-l,l-bis[4-[(trifluoroacetyl)-amino]phenyl]-1-hydroxy-3-butyl]amino-2-propanol 15 hydrochloride MS m/z: 614 (M++1) (free) (3) (2S)-1-Phenoxy-3-[(3RS)-l,l-bis[4-(propionylamino)-phenyl]-3-butyl]amino-2-propanol 20 MS m/z: 518 (M++1) Example 37 To a mixture of (2S)-1-phenoxy-3-[N-benzyl-[(3RS)-l,l bis(4-aminophenyl)-1-hydroxy-3-butyl]amino]-2-propanol (120 25 mg), acetic acid (3 ml) and water (0.6 ml), potassium cyanate (77 mg) was added. The reaction mixture was worked up in the usual manner to give (2S)-1-phenoxy-3-[N-benzyl-[(3RS)-1,1-bis(4-ureidophenyl)-1-hydroxy-3-butyl]amino]-2-propanol (65 mg ) .
30 MS m/z: 598 (M++1) Example 38 Formic acid (650 ~~1) and acetic anhydride (540 ~1) were mixed and started at room temperature for 30 minutes. The 35 mixture was added to a solution of (2S)-1-phenoxy-3-[N-benzyl-[(3RS)-1,1-bis(4-aminophenyl)-1-hydroxy-3-butyl]-amino]-2-propanol (325 mg) in dichloromethane (2 ml) at 0°C, warmed to room temperature and worked up in the usual manner.
The crude product was stirred with potassium carbonate (0.62 g) in methanol (4 ml) at room temperature for 4 hours and worked up in the usual manner to give (2S)-1-phenoxy-3-[N-benzyl-[(3RS)-1,1-bis[4-(formylamino)phenyl)-1-hydroxy-3-butyl)amino]-2-propanol (342.4 mg).
MS m/z: 568 (M++1) Example 39 To a mixture of lithium aluminum hydride (0.1 g) and tetrahydrofuran (1 ml), a solution of (2S)-1-phenoxy-3-[N-benzyl-[(3RS)-1,1-bis[4-(formylamino)phenyl]-1-hydroxy-3-butyl]amino]-2-propanol (280 mg) in tetrahydrofuran (2 ml) was added dropwise at 0°C. The reaction mixture was stirred for 2.5 hours and worked up in the usual manner to give (2S)-1-phenoxy-3-[N-benzyl-[(3RS)-1,1-bis[4-(methylamino)phenyl]-1-hydroxy-3-butyl]amino]-2-propanol (273 mg).
MS m/z: 540 (M++1) Example 40 (2S)-1-Phenoxy-3-[(3RS)-l,l-bis[4-[N-methyl-(methoxycarbonyl)amino]phenyl]-1-hydroxy-3-butyl]amino-2-propanol (30 mg) was obtained from (2S)-1-phenoxy-3-[N-benzyl-[(3RS)-l,l-bis[4-[N-methyl-(methoxycarbonyl)amino]-phenyl]-1-hydroxy-3-butyl]amino)-2-propanol (60 mg) by the usual hydrogenation.
MS m/z: 566 (M++1) Example 41 (1R)-1-[4-Hydroxy-3-(methanesulfonylamino)phenyl]-2-[[(3RS)-l,l-bis[4-[(methoxycarbonyl)amino]phenyl]-3-butyl)-amino]ethanol (14.3 mg) was obtained from (1R)-1-[4-bezyloxy-3-(methanesulfonylamino)phenyl]-2-[[(3RS)-l,l-bis[4-[(methoxycarbonyl)amino]phenyl]-3-butyl]amino]ethanol (46.1 mg) by hydrogenation in the usual manner.
MS m/z: 601 (M++1) Example 42 The following compound was obtained according to a similar manner to that of Example 41.
(2R)-3-[4-Hydroxy-3-(methanesulfonylamino)phenyl]-1-[(3RS)-1,1-bis(4-methoxyphenyl)-3-butyl]amino-2-propanol (5.0 mg) MS m/z: 529 (M++1) Example 43 A mixture of (R)-(4-benzyloxy-3-nitrophenyl)oxirane (34.4 mg), N-benzyl-[3,3-bis[4-(methoxycarbonylamino)phenyl]-propyl]amine (56.7 mg) and ethanol (2 ml) was heated under reflux for 12 hours. Iron powder, ammonium chloride and water was added to the reaction mixture and heating was continued for 1 hour. The reaction mixture was filtrated and worked up in the usual manner to give crude (1R)-1-(3-amino-4-benzyloxyphenyl)-2-[N-benzyl-[3,3-bis[4-[(methoxy-carbonyl)amino]phenyl]propyl]amino]ethanol (111.7 mg).
MS m/z: 689 (M++1) Example 44 The following compound was obtained according to a similar manner to that of Example 43.
(2S)-1-(3-Amino-4-benzyloxyphenoxy)-3-[N-benzyl-[3,3-bis[4-[(methoxycarbonyl)amino]phenyl]propyl]amino]-2-propanol MS m/z: 719 Example 45 Under nitrogen, to a solution of 4,4-bis(4-methoxyphenyl)-2-butanone (187 mg) and (1RS)-2-amino-1-(2-methylpyridin-6-yl)ethanol (100 mg) prepared from 6-methylpyridin-2-carboxaldehyde and trimethylsilylcyanide catalized with zinc iodide followed by reduction with lithium aluminum hydride, in 1,2-dichloroethane (10 ml) was added sodium triacetoxyborohydride (257 mg) at room temperatue, and the mixture was stirred at the same temperature for 24 hours.
The resulting mixture was poured into saturated aqueous sodium bicarbonate solution, and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was treated with 4N hydrogen chloride in 1,4-dioxane to afford (1RS)-2-[[(1RS)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]-amino]-1-(6-methylpyridin-2-yl)ethanol (140 mg) dihydrochloride.
MS m/z: 421 (M++1) (free) Example 46 Under nitrogen, to a solution of (2S)-3-[4-benzyloxy-3-(methanesulfonylamino)phenoxy]-1,2-epoxypropane (198 mg) and N-benzyl-[(1RS)-3,3-bis(4-hydroxyphenyl)-1-methylpropyl]amine (200 mg) in methanol (20 ml) was refluxed for 18 hours. The resulting mixture was poured into saturated aqueous sodium bicarbonate solution, and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was chromatographed (hexane-ethyl acetate) over silica gel to afford N-[5-[(2S)-3-[N-benzyl-[(1RS)-3,3-bis(4-hydroxyphenyl)-1-methylpropyl]amino]-2-hydroxypropoxy]-2-(benzyloxy)phenyl]methanesulfonamide (120 mg).
MS m/z: 696 (M++1) Example 47 Under nitrogen, to a solution of (2S)-3-[4-benzyloxy-3-(methanesulfonylamino)phenoxy]-1,2-epoxypropane (200 mg) and N-benzyl-[(IRS)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]amine (163 mg) in dichloromethane (10 ml) was added ytterbium(III) trifluoromethanesulfonate (1.0 g) at room temperature, and the mixture was stirred at the same temperature for 3 hours.
The resulting mixture was poured into saturated aqueous sodium bicarbonate solution, arid extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was chromatographed (hexane-ethyl acetate) over silica gel to afford N- [5- [ (2S) -3- [N-benzyl- [ (1RS) -3, 3-bis (4-methoxyphenyl)-1-methylpropyl]amino]-2-hydroxypropoxy]-2-(benzyloxy)phenyl]methanesulfonamide (50 mg).
MS m/z: 724 (M++1) _Example 48 Under nitrogen, to a solution of N-benzyl-[3,3-bis(4-hydroxyphenyl)-1-methylpropyl]amine (300 mg) and phenethyloxirane (130 mg) in a mixture of ethyl acetate (5 ml) and tetrahydrofuran (5 ml) was added ytterbium(III) trifluoromethanesulfonate (110 mg) at room temperature, and the mixture was stirred at the same temperature for 96 hours.
The resulting mixture was poured into saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was purified by column chromatography on silica gel (chloroform: methanol ==20:1) to give 1-[N-benzyl-[3,3-bis(4-hydroxyphenyl)-1-methylpropyl]amino]-4-phenyl-2-butanol (240 mg ) .
NMR (CDC13, d): 0.95-1.10 (3H, m), 1.45-2.9 (9H, m), 3.2-3.75 (3H, m), 3.75-3.9 (1H, m), 6.55-6.8 (4H, m), 6.85-7.3 (14H, m) Example 49 The following compound was obtained according to a similar manner to that of Example 48.

(2S)-1-[N-Benzyl-[(1RS)-3,3-bis(4-hydroxyphenyl)-1-methylpropyl]amino]-3-(phenylthio)-2-propanol NMR (CDC13, ~): 0.85-1.1 (3H, m), 1.7-3.1 (7H, m), 3.3-3.75 (3H, m), 3.75-3.9 (1H, m), 6.55-6.75 (4H, m), 5 6.8-7.25 (14H, m) Example 50 Under nitrogen, to a solution of N-[5-[(1R)-2-[N-benzyl-[(1RS)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]amino]-1-10 (triethylsilyloxy)ethyl]-2-(benzyloxy)phenyl]methane-sulfonamide (221 mg) in tetrahydrofuran (3 ml) were added acetic acid (63 ~tl) and tetrabutylammonium fluoride (1M
solution in tetrahydrofuran, 0.68 ml) at room temperature, and the mixture was stirred at the same temperature for 4.5 15 hours. The resulting mixture was poured into saturated aqueous sodium bicarbonate and extracted with ethyl acetate.
The organic layer~was washed with brine, dried over anhydrous magnesium sulfate, and evaporated in vacuo. The residue was purified by column chromatography on silica gel (hexane: ethyl 20 acetate = 2:1) to give N-[5-[(1R)-2-[N-benzyl-[(1RS)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]amino]-1-hydroxyethyl]-2-(benzyloxy)phenyl]methanesulfonamide (164 mg ) .
NMR (CDC13, d) : 0. 95-1. 1 (3H, m) , 1.7-2. 85 (5H, m) , 25 2.88 (3H, m), 3.35-4.05 (8H, m), 4.25-4.5 (1H, m), 5.08 (2H, m), 6.7-7.5 (21H, m) Example 51 A mixture of N-[5-[(1R)-2-[N-benzyl-[(1RS)-3,3-bis(4-30 methoxyphenyl)-1-methylpropyl]amino]-1-hydroxyethyl]-2-(benzyloxy)phenyl]methanesulfonamide (149 mg) and 10°s palladium on activated carbon (50°s wet, 50 mg) in methanol (5 ml) was stirred at room temperature in the presence of hydrogen at an atmospheric pressure for 6 hours. After 35 filtration, the filtrate was evaporated in vacuo, followed by treatment with 9N hydrogen chloride in ethyl acetate to give N-[5-[(1R)-2-[(1RS)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]-amino-1-hydroxyethyl]-2-hydroxyphenyl]methanesulfonamide hydrochloride (90 mg).
NMR (DMSO-d6, b): l.l-1.35 (3H, m), 1.9-2.2 (1H, m), 2.55-3.1 (7H, m), 3.70 (6H, m), 3.95-4.1 (1H, m), 4.7-4.9 (1H, m), 6.8-7.4 (11H, m) Example 52 The following compounds were obtained according to a similar manner to that of Example 51.
(1) 1-[3,3-Bis(4-hydroxyphenyl)-1-methylpropyl]amino-4-phenyl-2-butanol hydrochloride NMR (CD30D, ~): 1.1-1.5 (3H, m), 1.7-1.9 (2H, m), 1.95-2.2 (1H, m), 2.45-3.2 (6H, m), 3.6-4.0 (1H, m), 6.5-6.8 (4H, m), 7.0-7.35 (9H, m) (2) (2S)-1-Benzenesulfonyl-3-[(1RS)-3,3-bis(4-hydroxy-phenyl)-1-methylpropyl]amino-2-propanol hydrochloride NMR (CD30D, d): 1.25-1.4 (3H, m), 1.95-2.2 (1H, m), 2.45-2.7 (1H, m), 2.9-3.55 (5H, m), 3.85-4.0 (1H, m), 9.25-4.4 (1H, m), 6.65-6.85 (4H, m), 7.05-7.2 (4H, m), 7.6-7.8 (3H, m), 7.95-8.05 (2H, m) (3) (2S)-1-Phenoxy-3-[(3RS)-l,l-bis(4-ureidophenyl)-3-butyl]amino-2-propanol hydrochloride MS m/z: 492 (M++1) (free) Example 53 Under nitrogen, a solution of [(1S)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]amine (0.55 g), N-[2-benzyloxy-5-[(1R)-2-iodo-1-(triethylsilyloxy)ethyl]phenyl]-methanesulfonamide (1.1 g) and N,N-diisopropylethylamine (1.4 ml) in N,N-dimethylacetamide (5 ml) was stirred at 110°C for 24 hours. The resulting mixture was poured into saturated aqueous sodium bicarbonate and extracted with ethyl acetate.
The organic layer was washed successively with water and brine, dried over anhydrous sodium sulfate and evaporated in vacuo. Under nitrogen, to the residue in ethyl acetate (10 ml) was added 4N hydrogen chloride in ethyl acetate (2 ml) at 5°C, and the mixture was stirred at room temperature for 45 minutes. The resulting mixture was poured into saturated aqueous sodium bicarbonate and extracted with ethyl acetate.
The organic layer was washed with brine, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (chloroform: methanol = 50:1 to 20:1) to give N-[2-benzyloxy-5-[(1R)-2-[(1S)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]-amino-1-hydroxyethyl]phenyl]methanesulfonamide (0.65 g).
NMR (CDC13, ~): 1.09 (3H, d, J=6.3Hz), 1.85-2.3 (2H, m), 2.35-2.6 (2H, m), 2.9-3.2 (4H, m), 3.76 (6H, s), 4.0-4.1 (1H, m), 4.45-4.6 (1H, m), 5.10 (2H, m), 6.82 (4H, d, J=8.lHz), 6.96 (1H, d, J=8.5Hz), 7.1-7.2 (5H, m), 7.35-7.5 (6H, m) Example 54 The following compounds were obtained according to a similar manner to that of Example 53.
(1) N-[2-Benzyloxy-5-[(1R)-2-[(1R)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]amino-1-hydroxyethyl]phenyl]-methanesulfonamide NMR (CDC13, b): 1.08 (3H, d, J=6.2Hz), 1.9-2.2 (2H, m), 2.5-2.85 (3H, m), 2.90 (3H, s), 3.76 (6H, s), 4.03 (1H, t, J=8.2Hz), 4.47 (1H, dd, J=3.6 and 8.5Hz), 5.10 (2H, s), 6.8-6.9 (4H, m), 6.96 (1H, d, J=8.5Hz), 7.1-7.2 (5H, m), 7.35-7.5 (6H, m) (2) N-[2-Benzyloxy-5-[(1R)-2-[(1RS)-3,3-bis(4-hydroxy-phenyl)-1-methylpropyl]amino-1-hydroxyethyl]phenyl]-methanesulfonamide NMR (DMSO-d6, ~): 1.0-1.1 (3H, m), 1.7-1.95 (1H, m), 2.1-2.85 (4H, m), 2.90 (3H, s), 3.8-3.95 (1H, m), 4 .5-4. 6 (1H, m) , 5. 17 (2H, s) , 6. 6-6.75 (4H, m) , 6.95-7.2 (6H, m), 7.25-7.6 (6H, m) _Example 55 A mixture of N-(2-(benzyloxy)-5-[(1R)-2-[(1S)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]amino-1-hydroxyethyl]phenyl]-methanesulfonamide (620 mg) and loo palladium on activated carbon (50°s wet, 300 mg) in methanol (10 ml) was stirred at room temperature in the presence of hydrogen at an atmospheric pressure for 7.5 hours. After filtration, the filtrate was evaporated in vacuo. The residue was purified by column chromatography on silica gel (chloroform:methanol =
20:1 to 10:1), followed by treatment with 4N hydrogen chloride in ethyl acetate to give N-[5-[(1R)-2-[(1S)-3,3-bis( 4-methoxyphenyl)-1-methylpropyl]amino-1-hydroxyethyl]-2-hydroxyphenyl]methanesulfonamide hydrochloride (290 mg) NMR (DMSO-d6, b): 1.15-1.4 (3H, m), 1.85-2.2 (1H, m), 2.4-3.2 (7H, m), 3.70 (6H, s), 3.95-4.1 (1H, m), 4.7-4.9 (1H, m), 6.7-7.4 (11H, m) _Example 56 The following compounds were obtained according to a similar manner to that of Example 54.
(1) N-[5-[(1R)-2-[(1R)-3,3-Bis(4-methoxyphenyl)-1-methylpropyl]amino-1-hydroxyethyl]-2-hydroxyphenyl]methanesulfonamide hydrochloride NMR (DMSO-d6, b): 1.15-1.4 (3H, m), 1.9-2.15 (1H, m), 2.4-3.15 (7H, m), 3.70 (6H, m), 3.95-4.1 (1H, m), 4.75-4.9 (1H, m), 6.8-7.4 (11H, m) (2) N-[5-[(1R)-2-[[3,3-Bis(4-hydroxyphenyl)-1-methylpropyl]-amino]-1-hydroxyethyl]-2-hydroxyphenyl]-methanesulfonamide hydrochloride NMR (DMSO-d6, ~): 1.15-1.3 (3H, m), 1.85-2.1 (1H, m), 2.55-3.2 (7H, m), 3.8-4.0 (1H, m), 4.7-4.9 (1H, m), 6.6-6.75 (4H, m), 6.9-7.3 (7H, m) (3) (2S)-1-(6-Aminopyridin-3-yloxy)-3-[[(1RS)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]amino]-2-propanol trihydrochloride, starting from the objective compound of Example 57.
NMR (DMSO-d6, d): 1.05-1.4 (3H, m), 1.9-2.2 (1H, m), 2.5-3.2 (4H, m), 3.55-3.85 (7H, m), 3.85-4.3 (3H, m), 6.9-7.4 (9H, m), 7.5-7.9 (2H, m) Example 57 A mixture of [3,3-bis(4-methoxyphenyl)-1-methylpropyl]-amine and (2S)-3-[2-(benzyloxycarbonylamino)pyridin-5-yloxy]-1,2-epoxypropane (98 mg) in methanol (5 ml) was refluxed for 19 hours. After removal of the solvent in vacuo, the residue was purified by column chromatography on silica gel (chloroform:methanol = 30:1 to 20:1) to give [5-[(2S)-3-[(1RS)-3,3-bis(4-methoxyphenyl)-1-methylpropyl]amino-2-hydroxypropoxy]pyridin-2-yl]carbamic acid benzyl ester (110 mg).
NMR (CDC13, b): 1.1-1.2 (3H, m), 1..7-2.3 (2H, m), 2.45-2.6 (2H, m), 2.7-2.75 (1H, m), 3.76 (6H, s), 3.85-3.95 (3H, m), 4.0-4.1 (1H, m), 5.22 (2H, s), 6.8 (4H, d, J=8.6Hz), 7.1-7.45 (lOH, m), 7.9-7.95 (2H, m) Example 58 To a solution of (2S)-1-[N-benzyl-[(1RS)-3,3-bis(4-hydroxyphenyl)-1-methylpropyl]amino]-3-phenylthio-2-propanol (300 mg) in methanol (10 ml) was added OXONE~ (potassium peroxymonosulfate) (710 mg) in water (2 ml) at room temperature, and the mixture was stirred at the same temperature for 4 hours. The resulting mixture was poured into a mixture of ethyl acetate and water, and was made basic 5 with saturated aqueous sodium bicarbonate. After separation, the organic layer was washed with brine, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel (chloroform: methanol = 20:1) to give (2S)-1-benzenesulfonyl-10 3-[N-benzyl-[(1RS)-3,3-bis(4-hydroxyphenyl)-1-methylpropyl]am ino]-2-propanol (220 mg).
NMR (CDC13, ~): 0.9-1.1 (3H, m), 1.75-2.3 (2H, m), 2.35-2.7 (3H, m), 2.9-3.25 (2H, m), 3.3-4.0 (4H, m), 6.65-6.8 (4H, m), 6.9-7.35 (9H, m), 7.5-7.7 15 (3H, m), 7.75-7.9 (2H, m) Example 59 A mixture of (2S)-1-phenoxy-3-[N-benzyl-[3,3-bis[4-(methoxycarbonyl)phenyl]propyl]amino]-2-propanol (103 mg), 20 methanol (2 ml), 1,4-dioxane (2 ml) and 1N aqueous sodium hydroxide solution (1 ml) was stirred at 50°C for 2 hours.
The reaction mixture was acidified with 3N hydrochloric acid (1 ml) and worked up in a usual manner to give (2S)-1-phenoxy-3-[N-benzyl-[3,3-bis(4-carboxyphenyl)propyl]amino]-2-25 propanol (75.1 mg).
Example 60 A mixture of (2S)-1-phenoxy-3-[N-benzyl-[3,3-bis(4-carboxyphenyl)propyl]amino]-2-propanol (75 mg), 30 diphenylphosphoryl azide (96 mg), triethylamine (58 ~l), toluene (1 ml) and 1,4-dioxane (1 ml) was stirred at 50°C for 0.5 hour, then at 100°C for 45 minutes. Methanol (1 ml) was added to the reaction mixture, and the heating was continued for 15 hours. The reaction mixture was worked up in a usual 35 manner followed by purification by preparative thin-layer chromatography to afford (2S)-1-phenoxy-3-[N-benzyl-[3,3-bis[4-[(methoxycarbonyl)amino]phenyl]propyl]amino]-2-propanol (21.5 mg).
MS m/z: 598 (M++1) _Example 61 (2S)-1-Phenoxy-3-[N-benzyl-[3,3-bis[4-[(methoxy-carbonyl)amino]phenyl]propyl]amino]-2-propanol (18.8 mg) was hydrogenated in a usual manner to give (2S)-1-phenoxy-3-[[3, 3-bis[4-[(methoxycarbonyl)amino]phenyl]propyl]amino]-2-propanol (8.1 mg).
IR (KBr): 1710 (s), 1601 (m), 1537 (s), 1315 (w), 1238 (s), 1070 (m) cm-1 NMR (MeOH-d4, d): 2.2-2.3 (2H, m), 2.6-2.9 (4H, m), 3.72 (6H, s), 3.9-4.1 (4H, m), 6.9-7.0 (3H, m), 7.2-7.4 (lOH, m) MS m/z: 508 (M++1)

Claims (11)

1. A compound of the general formula [I]:
wherein A is a heterocyclic group or aryl, each of which may have 1 to 3 same or different substituent(s) selected from a group consisting of halogen, hydroxy, amino, lower alkyl, lower alkylsulfonylamino, phenyl(lower)alkoxy and phenyl(lower)alkoxycarbonylamino, -X- is bond, -CH2-, -CH2-CH2-, -NH-CH2-, -O-CH2-, -S-CH2-, -SO-CH2- or -SO2-CH2-, (in which R11 is hydrogen, hydroxy, lower alkoxy or acyloxy) and -Z- is -(CH2)n-Q-(CH2)m-, -(CH2)n-CH=CH-(CH2)m- or -(CH2)n-C~C-(CH2)m- (in which -Q- is -O-, -S-, -SO-, -SO2-, , -CO- or wherein R10 is hydrogen or lower alkyl, and R11 is lower alkyl, R6, R7, R8 and R9 are each independently hydrogen, hydroxy, lower alkyl, lower alkenyl, lower alkoxy, lower alkoxy(lower)alkyl or aryl which may have 1 to 3 lower alkoxy, n, m and k is each independently 0 to 6, p is 0 to 4, q is 1 to 4, and r is 2 to 7) and (in which i is 0 to 6), R1 is hydrogen or an amino protective group, and R2, R3, R4 and R5 are each independently hydrogen;
lower alkyl; lower alkylthio; lower alkylsulfonyl;
hydroxy; lower alkoxy;
amino; lower alkylamino; acylamino; N-(lower alkyl)acylamino; carboxy; lower alkoxycarbonyl;
carbamoyl optionally substituted with one or two lower alkyl; hydroxy(lower)alkyl; lower alkoxy(lower)alkyl;
N-acylamino(lower)alkyl; N-(lower alkyl)-N-acylamino(lower)alkyl; carboxy(lower)alkyl;
lower alkoxycarbonyl(lower)alkyl; carbamoyl(lower)alkyl optionally substituted with one or two lower alkyl; or (in which R12 and R13 are each independently hydrogen or lower alkyl, or R12 and R13 may be bonded to form a lower alkylene chain, and j is 0 to 6), and a salt thereof.
2. A compound of claim 1, wherein A is pyridyl, indolyl, 2-oxo-2,3-dihydro-1H-benzimidazolyl or phenyl, each of which may have 1 to 3 same or different substituent(s) selected from a group of hydroxy, amino, lower alkyl, lower alkylsulfonylamino, phenyl(lower)alkoxy and phenyl(lower)alkoxycarbonylamino, -X- is bond, -CH2-, -CH2-CH2-, -O-CH2- or -SO2-CH2-, (in which R11 is hydrogen or hydroxy) and -Z- is -(CH2)n-Q-(CH2)m- (in which -Q- is , wherein R10 is hydrogen or lower alkyl and R11 is lower alkyl, R6, R7, R8 and R9 are each independently hydrogen, lower alkyl or aryl which may have 1 to 3 lower alkoxy, n, m and k is each independently 0 to 6, and r is 2 to 7) and ~~(in which i is 0 to 6).
R1 is hydrogen or ar(lower)alkyl, and R2, R3, R4 and R5 are each independently hydrogen;
lower alkyl; lower alkylthio; lower alkylsulfonyl;
hydroxy; lower alkoxy; amino; lower alkylamino;
acylamino; N-(lower alkyl)acylamino; carboxy; or lower alkoxycarbonyl.
3. A compound of claim 2, wherein A is pyridyl, indolyl or phenyl, each of which may have 1 to 3 same or different substituent(s) selected from a group of hydroxy, amino, lower alkyl, lower alkylsulfonylamino, phenyl(lower)alkoxy and phenyl(lower)alkoxycarbonylamino, -X- is bond, -CH2-, -CH2-CH2-, -O-CH2- or -SO2-CH2-, (in which R11 is hydrogen or hydroxy) and -Z- is or -(CH2)n-Q-(CH2)m- (in which -Q- is wherein R10 is hydrogen or lower alkyl and R11 is lower alkyl, R6, R7, R8 and R9 are each independently hydrogen, lower alkyl or phenyl which may have 1 to 3 lower alkoxy, n, m and k is each independently 0 or 1, and r is 2 to 7) and (in which i is 0 or 1), R1 is hydrogen or phenyl(lower)alkyl, and R2, R3, R4 and R5 are each independently hydrogen;
lower alkyl; lower alkylthio; lower alkylsulfonyl;
hydroxy; lower alkoxy; amino; lower alkylamino;
lower alkoxycarbonylamino; lower alkylsulfonylamino; lower alkanoylamino; ureido;
trifluoroacetylamino; N-(lower alkyl)-[(lower)alkoxycarbonyl]amino; carboxy; or lower alkoxycarbonyl.
4. A compound of claim 3, whrein A is phenyl which may have 1 to 3 same or different substituent(s) selected from a group of hydroxy, amino, lower alkylsulfonylamino and phenyl(lower)alkoxy, -X- is bond, -CH2-, -CH2-CH2-, -O-CH2- or -SO2-CH2-, (in which R11 is hydrogen or hydroxy), -Z- is~ (in which R6, R7, R8 and R9 are each independently hydrogen, lower alkyl or phenyl which may have 1 to 3 lower alkoxy, n, m and k is each independently 0 or 1), R1 is hydrogen or phenyl(lower)alkyl, and R2, R3, R4 and R5 are each independently hydrogen;
lower alkyl; lower alkylthio; lower alkylsulfonyl;
hydroxy; lower alkoxy; amino; lower alkylamino;
lower alkoxycarbonylamino; lower alkylsulfonylamino; lower alkanoylamino; ureido;
trifluoroacetylamino; N-(lower alkyl)-[(lower)alkoxycarbonyl]amino; carboxy; or lower alkoxycarbonyl.
5. A compound of claim 4, wherein A is phenyl which may have 1 or 2 same or different substituent(s) selected from a group consisting of hydroxy, amino and lower alkylsulfonylamino, -X- is bond or -O-CH2-, , -Z- is , R1 is hydrogen, and R2, R3, R4 and R5 are each independently hydrogen, lower alkoxy or lower alkoxycarbonylamino.
6. A compound of claim 5, which is (2S)-1-[4-hydroxy-3-(methanesulfonylamino)phenoxy]-3-[[3,3-bis(4-methoxyphenyl)propyl]amino]-2-propanol;
(1R)-1-[4-hydroxy-3-(methanesulfonylamino)phenyl]-2-[[3,3-bis(4-methoxyphenyl)propyl]amino]ethanol;
(2S)-1-phenoxy-3-[[3,3-bis[4-[(methoxycarbonyl)amino]-phenyl]propyl]amino]-2-propanol;
or a salt thereof.
7. A process for preparing a compound of claim 1, or a salt thereof, which comprises, (i) reacting a compound [II] of the formula :
wherein A and X are each as defined in claim 1, with a compound [III] of the formula :
wherein Y, Z, R1, R2, R3, R4 and R5 are each as defined in claim 1, or a salt thereof, to give a compound [I] of the formula:
wherein A, X, Y, Z, R1, R2, R3, R4 and R5 are each as defined in claim 1, or a salt thereof, or (ii) subjecting a compound [Ia] of the formula :
wherein A, X, Y, Z, R2, R3, R4 and R5 are each as defined in claim 1, and R ~ is an amino protective group, or a salt thereof, to elimination reaction of the amino protective group, to give a compound [Ib] of the formula :
wherein A, X, Y, Z, R2, R3, R4 and R5 are each as defined in claim 1, or a salt thereof.
8. A pharmaceutical composition which comprises, as an active ingredient, a compound of claim 1 or a pharmaceutically acceptable salt thereof in admixture with pharmaceutically acceptable carriers or excipients.
9. Use of a compound of claim 1 or a pharmaceutically acceptable salt thereof for the manufacture of a medicament.
10. A compound of claim 1 or a pharmaceutically acceptable salt thereof for use as a medicament.
11. A method for the prophylactic and/or the therapeutic treatment of pollakiuria or urinary incontinence which comprises administering a compound of claim 1 or a pharmaceutically acceptable salt thereof to a human being or an animal.
CA002341458A 1998-08-26 1999-08-23 Aminoalcohol derivatives and their use as beta 3 adrenergic agonists Abandoned CA2341458A1 (en)

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AUPR034000A0 (en) 2000-09-25 2000-10-19 Fujisawa Pharmaceutical Co., Ltd. Aminoalcohol derivatives
AUPR120400A0 (en) * 2000-11-02 2000-11-23 Fujisawa Pharmaceutical Co., Ltd. New compound
JP4044740B2 (en) * 2001-05-31 2008-02-06 信越化学工業株式会社 Resist material and pattern forming method
WO2003024483A1 (en) * 2001-09-11 2003-03-27 Fujisawa Pharmaceutical Co., Ltd. Potentiator for inhibitory effects on urinary frequency and urinary incontinence
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DE102004050952A1 (en) * 2004-10-18 2006-04-20 Boehringer Ingelheim Pharma Gmbh & Co. Kg Use of a beta-3-adrenoreceptor-agonist for the prophylaxis and/or treatment of e.g. benign prostata hyperplasia and/or its associated symptoms and chronic pelvic base pain syndrome, pelvic myoneuropathy, prostatodynia or prostatopathy
EP2096105A1 (en) * 2008-02-28 2009-09-02 Laboratorios Almirall, S.A. Derivatives of 4-(2-amino-1-hydroxyethyl)phenol as agonists of the b2 adrenergic receptor

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