US 5,629,200 A · Production of optically active 2-amino-1-phenylethanol derivatives by asymetrical assimilation

Abstract

An (R)-2-amino-1-phenylethanol derivative shown by the general formula (IIa) ##STR1## wherein R.sup.1 and R.sup.5 represent a hydrogen atom, etc.; R.sup.2, R.sup.3 and R.sup.4 independently represent a halogen atom, etc., or a salt thereof, can readily be produced (1) by permitting a microorganism to act on a mixture of corresponding (R)-form and (S)-form to asymmetrically utilize, or (2) by permitting a microorganism to act on a corresponding aminoketone derivative to asymmetrically reduce. An (R,R)-1-phenyl-2-[(2-phenyl-1-alkylethyl) amino]ethanol derivative having a high optical purity can easily be obtained from the compound of the formula (IIa) or a salt thereof. Said derivative is useful as an intermediate for producing an anti-obesity agent.

A process for separating an optically active 2-amino-1-phenylethanol derivative from a mixture of enantiomers of said derivative which comprises:

(1) treating a mixture of enantiomers of 2-amino-1-phenylethanol compound shown by the general formula (I) ##STR19## or a salt thereof, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 are, the same or different, and are selected from the group consisting of:
(1) a hydrogen atom;
(2) a halogen atom;
(3) a C.sub.1-4 alkyl group or a C.sub.1-4 alkyl group substituted with a substituent selected from the group consisting of a hydroxyl group, a C.sub.1-4 alkoxy group, benzoyl group, a C.sub.6-12 aryl group or a C.sub.6-12 aryl group substituted with a C1-4 alkoxy group, a C.sub.1-4 alkylthio group and a halogen atom;
(4) a hydroxyl group, or a hydroxyl group protected with a protective group;
(5) a C.sub.1-4 alkoxy group, or a C.sub.1-4 alkoxy group substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group and a C.sub.1-4 alkoxy group;
(6) a C.sub.3-10 cycloalkyloxy group, or a C.sub.3-10 cycloalkyloxy group substituted with a substituent selected from the group consisting of a C.sub.1-4 alkyl group a hydroxyl group and a halogen atom;
(7) a C.sub.7-20 aralkyloxy group, or a C.sub.7-20 aralkyloxy group substituted with a substituent selected from the group consisting of a C.sub.1-4 alkyl group, a C.sub.6-12 aryl group, a hydroxyl group, a C.sub.1-4 alkoxy group, a nitro group and a halogen atom;
(8) a C.sub.6-16 aryloxy group, or a C.sub.6-16 aryloxy group substituted with a substituent selected from the group consisting of a C.sub.1-4 alkyl group, a hydroxyl group, a C.sub.1-4 alkoxy group, a nitro group and a halogen atom;
(9) a C.sub.1-4 alkylthio group, or a C.sub.1-4 alkylthio group substituted with a substituent selected from the group consisting of a halogen atom, a hydroxyl group and a C.sub.1-4 alkoxy group;
(10) an acyl group selected from the group consisting of (a) a C.sub.1-16 acyl group, or a C.sub.1-6 acyl group substituted with a substituent selected from the group consisting of a hydroxyl group, a C.sub.1-4 alkoxy group, a C.sub.1-4 alkylthio group and a halogen atom, (b) a C.sub.7-20 acyl group having an aromatic ring or a C.sub.7-20 acyl group having an aromatic ring substituted with a substituent selected from the group consisting of a C.sub.1-4 alkyl group, a hydroxyl group, a C.sub.1-4 alkoxy group, a nitro group and a halogen atom, and (c) an acyl group having a heterocyclic ring, or an acyl group having a heterocyclic ring substituted with a substituent selected from the group consisting of a C.sub.1-4 alkyl group, a hydroxyl group, a C.sub.1-4 alkoxy group, a nitro group and a halogen atom;
(11) a carboxyl group, or a carboxyl group protected with a protective group;
(12) a C.sub.2-5 alkoxycarbonyl group, or a C.sub.2-5 alkoxycarbonyl group substituted with a substituent selected from the group consisting of a hydroxyl group, a C.sub.1-4 alkoxy group and a halogen atom;
(13) a nitro group;
and
(14) an amino group, or an amino group substituted with a substituent selected from the group consisting of (a) a C.sub.1-4 alkyl group, or a C.sub.1-4 alkyl group substituted with a substituent selected from the group consisting of a hydroxyl group, a C.sub.1-4 alkoxy group, a benzoyl group, a C.sub.1-4 alkylthio group and a halogen atom, (b) a C.sub.7-20 aralkyl group, or a C.sub.7-20 aralkyl group substituted with a substituent selected from the group consisting of a C.sub.1-4 alkyl group, a hydroxyl group, a C.sub.1-4 alkoxy group, a nitro group and a halogen atom, (c) a C.sub.1-6 acyl group, or a C.sub.1-6 acyl group substituted with a substituent selected from the group consisting of a hydroxyl group, a C.sub.1-4 alkoxy group, a C.sub.1-4 alkylthio group and a halogen atom, (d) a C.sub.7-20 acyl group having an aromatic ring, or a C.sub.7-20 acyl group having an aromatic ring substituted with a substituent selected from the group consisting of a C.sub.1-4 alkyl group, a hydroxyl group, a C.sub.1-4 alkoxy group, a nitro group and a halogen atom, (e) an acyl group having a heterocyclic ring, or an acyl group having a heterocyclic ring substituted with a substituent selected from the group consisting of a C.sub.1-4 alkyl group, a hydroxyl group, a C.sub.1-4 alkoxy group, a nitro group and a halogen atom, and (f) a carboxyl group, or a carboxyl group protected with a protective group, wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4 and R.sup.5 are not concurrently hydrogen atoms,
with a microorganism, or a preparation derived therefrom, which is capable of selectively utilizing a corresponding (S)-form of said compound or a salt thereof, and allowing said microorganism or a preparation thereof to selectively utilize the (S)-form of said compound or a salt thereof, wherein said microorganism is a strain of microorganism selected from the group consisting of Hansenula anomala, Geotrichum candidum, Candida albicans, Candida parapsilosis, Candida gropengiesseri, Candida aaseri, Candida beechii, Candida atmospherica, Candida natalensis, Candida paludigena, Candida sake, Candida pintolopesii var. pintolopesii, Cryptococcus neoformans, Rhodosporidium sphaerocarpum, Rhodosporidium diobovatum, Rhodotorula rubra, Rhodotorula glutinis var. dairenensis, Saccharomyces montanus, Sporobolomyces roseus, Kluyveromyces marxianus var. bulgaricus, Kluyveromyces lactis, Issatchenkia scutulata var. scutulata, Pichia thermotolerans, Pichia farinosa, Botryoascus synnaedendrus, Debaryomyces hansendi var. hansendi, Lipomyces starkeyi, Metschnikowia bicuspidata, Saccharomycodes ludwigdi, Schizoblastosporion kobayashii, Stephanoascus ciferrii, Sterigmatomyces halophilus, Zygosaccharomyces rouxii, Zygosaccharomyces fermentati, Sporidiobolus salmonicolor, Sporidisbolus pararoseus, Malassezia furfur, Torulaspora delbrueckii, Corynebacterium aquaticum, Corynebacterium mediolanum, Gluconobacter asaii, Gluconobacter oxydans, Gluconobacter frateurii, Promicromonospora citrea, Pseudomonas aeruginosa, Pseudomonas riboflavina, Pseudomonas fluorescens, Pseudomonas putida, Pseudomonas syncyanea, Pseudomonas diminuta, Pseudomonas chlororaphis, Pseudomonas fragi, Pseudomonas sp. ATCC 14676, Bordetella bronchiseptica, Acetobacter sp. IFO 3248, Acetobacter sp. IFO 3297, Acetobacter pasteurianus, Agrobacterium radiobacter, Arthrobacter ureafaciens, Amauroascus reticulatus, Brevibacterium linens, Micrococcus roseus, Aureobacterium testaceum, Azotobacter vinelandii, Xanthomonas campestris pv oryzae, Klebsiella pneumoniae, Comamonas testosteroni, Mycobacterium diernhoferi, Terrabacter tumescens, Agrocybe cylindracea, Trichoderma viride, Alternaria kikuchiana, Hamigera avellanea, Moniliella acetoabutans, Pholiota nameko, Podospola carbonaria, Aegerita candida, Streptomyces cinereoruber, Saccharomycopsis capsularis and Leucosporidium scottii to yield the corresponding (R) form of said compound;
and
recovering the (R)-form of said compound or a salt thereof.

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Production of optically active 2-amino-1-phenylethanol derivatives by asymetrical assimilation

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Production of optically active 2-amino-1-phenylethanol derivatives by asymetrical assimilation

Life of this patent

Abstract

Claims4