Patent Application
20230142248
This application claims priority to Chinese Patent Application No. 201910705432.5, dated Aug. 1, 2020 and entitled “METHOD FOR RACEMIC PREPARATION OF CHIRAL 13-AMINO ACIDS AND DERIVATIVES THEREOF”, the disclosure of which is herein incorporated by reference in its entirety.
The present disclosure relates to the field of medical synthesis, and relates to a method for a racemic preparation of chiral β-amino acids and derivatives thereof, in particular to a method for a racemic recycling of sitagliptin and intermediates thereof.
Sitagliptin, with a chemical name (2R)-4-oxo-4-[3-trifluoromethyl-5,6-dihydro[1,2,4]triazole[4,3-a]pyrazine-7(8H)-yl]-1-(2,4,5-trifluorophenyl)-butan-2-amine, the structural formula is list as below:
It is the first product of dipeptidyl peptidase-IV (DPP-IV) developed by Merck (US). In October 2006, its phosphate hydrate was approved by the US FDA as the first dipeptidyl peptidase-IV (DPP-IV) for the clinical treatment for clinically treating type 2 diabetes. The medicine has the advantages of fewer adverse reactions, low risk of hypoglycemia and no weight gain.
The key to the synthesis of sitagliptin lies in the construction of the chiral amino group in its β-amino acid structure. The current common methods for constructing this type of structure include the asymmetric hydrogenation method and chiral induction method, but this method has problems such as difficulty in preparing catalysts and ligands, and high cost. In addition, the catalytic synthesis method is also an important method for the construction of chiral β-amino acid, but this method has problems such as complex equipment required and poor stability, which also limits its industrial application to a certain extent. Therefore, the conventional chiral resolution method is still the mainstream method for the industrial preparation of chiral β-amino structure compounds, but most of the remaining enantiomers cannot be effectively recovered, resulting in problems such as high three-waste, high production costs and waste of resources and the like. Therefore, how to solve the problem of the racemization of the chiral β-amino group is the key to the industrial production of sitagliptin.
In 2010, Satyanarayana et al. (WO2010122578) reported that the key β-amino intermediate of sitagliptin was resolved and the remaining S-isomer III reacted with sodium nitrite and sulfuric acid to undergo a recrystallization reaction and converted into alcohol IV. The recovery of the racemic I can be obtained by oxidizing, aminating, reduction. The method has long steps, complicated operations, and serious environmental pollution, poor industrial feasibility.
In 2011, Lipeng Zhang et al. (CN102319142) reported that the remaining S-isomer III after the resolution was condensed with aromatic aldehydes to synthesize imine II, followed by palladium-catalyzed hydrogenation and debenzylation to recover the racemic β-amino isomer I. This method still has long steps, the yield is low, and expensive heavy metal palladium is needed, which is expensive, so it is difficult to realize industrial production.
In 2014, Jiansheng Xia et al. (CN04130149) reported that the amino group in the S-isomer was chlorinated to obtain an intermediate IX, and then one molecule of hydrogen chloride was eliminated under alkaline conditions to obtain enamine intermediate VI, which was then reduced by hydrogenation to obtain β-amino racemate I. The method has long steps, a large amount of chlorinated reagents and a large amount of alkali are required. Operation is complicated, and high environmental protection pressure exists. Therefore, it is difficult to industrialize feasibility.
Journal of Organic Chemistry, 71(19), 7288-7292; 2006 discloses that (S)-4-phenyl-2-butylamine was refluxed for 2 hours under the conditions of methyl thioglycolate, benzene and AIBN to obtain 4-phenyl-2-butylamine:
This method can realize the racemization of the chiral amino group in one step, but it also has certain shortcomings: 1) It needs to use the equivalent sulfide, which has a large taste, serious pollution and high cost; 2) It needs to use 0.6 times the equivalent of the initiator AIBN, and needs to be fed in batches, the operation is complicated and cumbersome; 3) There is no report on the racemization of β-amino acid and derivatives thereof in this method.
In view of the importance of the method for a racemic preparation of chiral β-amino acid and derivatives thereof in the synthesis of sitagliptin intermediates, it is necessary to research and develop a new process to solve the current problems. The process needs to have the advantages such as convenient raw materials and easy operation, low cost, environmentally friendly, and economic and efficiency etc. Based on this, the present disclosure has developed a method for a racemic preparation of β-amino acid and derivatives thereof, in which the amount of sulfide and initiator can be reduced to 1% at most, and the initiator can be fed at one time, which is convenient to operate and environmentally friendly. It can be adapted to industrial production. The specific reaction is as follows:
Chiral ββ-amino acids and derivatives thereof cause sulfides to form sulfur free radicals in the presence of initiators, and the sulfur free radicals extract hydrogen from the carbon atom connected to the amino group, thereby realizing the racemization of the amino group.
Embodiments of the present disclosure provide a racemization manufacturing method for a racemic preparation of chiral β-amino acids of sitagliptin intermediate and derivatives thereof. The raw materials are easy to obtain, the cost is low, and the yield is high, and the method is suitable for industrialized production.
In order to achieve the objects of the present disclosure, the present disclosure provides the following technical solutions:
In a first aspect, the present disclosure provides a method for a racemic preparation of chiral β-amino acids and derivatives thereof, comprising the steps of:
racemizing a compound of formula I′ under conditions of initiator, sulfide and solvent to obtain a compound of formula II′, wherein a reaction equation is:
where R1 is hydrogen, alkyl or aryl; R1 may preferably be trifluorophenyl.
R2 is hydrogen, alkyl or aryl; R2 may preferably be hydrogen.
R3 is hydrogen, alkyl, aryl or acyl; may preferably be hydrogen.
R4 is alkyl, aryl, OR′, SR′, NHR′ or NR′R″, where R′ or R″ is hydrogen, alkyl or aryl. R4 may preferably be ethoxy, tert-butoxy or isopropoxy.
The sulfide comprises, but not limited to, methyl mercaptoacetate, methyl mercaptopropionate, methyl mercaptobutyrate, ethyl mercaptoacetate, 1-hexyl mercaptan, 1-heptane mercaptan, 1-octyl mercaptan, 1-nonane mercaptan, 1-decane mercaptan, benzyl mercaptan, phenyl ethyl mercaptan, furfuryl mercaptan, dodecane mercaptan and other alkyl mercaptans; 1,6-hexanedithiol, 3-propanedithiol, dimercaptoethyl sulfide, pentaerythritol tetra-3-mercaptopropionate (PETMP), trimethylolpropane tris(3-mercaptopropionate) (TMMP) and other polythiols; mercaptopropyltrimethoxysilane, 3-mercaptopropyltriethoxysilane and other mercapto-containing compounds; dialkyl disulfide, thiophenol, substituted thiophenol and various aromatic thiophenol, diphenyl disulfide and diaryl disulfide, preferably pentaerythritol tetra-3-mercaptopropionate (PETMP) or trimethylolpropane tris(3-mercaptopropionate) (TMMP).
The solvent comprises, but not limited to, one or more from a group consisting of benzene, toluene, o-xylene, m-xylene, p-xylene, nitrobenzene, chlorobenzene, tetrahydrofuran, 2-methyltetrahydrofuran, 1,4-dioxane, anisole, acetonitrile, chloroform, carbon tetrachloride, n-heptane, and n-octane, preferably toluene (TOL) or xylene.
The initiator comprises, but not limited to, azobisisobutyronitrile (AIBN), azobisisovaleronitrile (AMBN), azobisisoheptonitrile (ABVN), azobisisobutamidine hydrochloride (AIBA), dimethyl azobisisobutyrate (V601, AIBME), azobisisobuimidazoline hydrochloride (AIBI), azo isobutylcyanide formamide and other azo initiator (V30); dibenzoyl peroxide (BPO), lauryl peroxide (LPO), Diisopropyl peroxydicarbonate (IPP), dicyclohexyl peroxydicarbonate (DCPD), di-tert-butyl peroxide (DTB), m-chloroperoxybenzoic acid (m-CPBA), potassium persulfate (K2S2O8) and other peroxide initiators, preferably azobisisobutyronitrile (AIBN), azobisisovaleronitrile (AMBN) and azobisisoheptonitrile (ABVN).
A reaction temperature is 30° C. to 120° C., preferably 60° C. to 100° C.
A reaction time is 4 to 36 hours, preferably 18 to 24 hours.
A molar ratio of the initiator, the sulfide and a chiral β-amino substrate required for the reaction is that: initiator: sulfide: substrate is (0.01˜0.20): (0.01˜0.20):1.
In a second aspect, the present disclosure provides a method for a racemic preparation of chiral β-amino acids and derivatives thereof, comprising the steps of:
racemizing a compound of formula I″ under conditions of initiator, sulfide and solvent to obtain a compound of formula II″, wherein a reaction equation is:
where definitions of R3, R4 are the same as that above mentioned.
The definition of the sulfide is the same as that above mentioned.
The definitions of the solvent is the same as that above mentioned.
The definitions of the initiator is the same as that above mentioned.
The definitions of the reaction temperature is the same as that above mentioned.
The definitions of the reaction time is the same as that above mentioned.
A molar ratio of the initiator, the sulfide and a chiral β-amino substrate required for the reaction is that: initiator: sulfide: substrate is (0.01˜0.20): (0.01˜0.20):1.
In a third aspect, the present disclosure provides a method for a racemic preparation of chiral β-amino acids and derivatives thereof, comprising the steps of:
racemizing a compound of formula I′″ under conditions of initiator, sulfide and solvent to obtain a compound of formula II″, wherein a reaction equation is:
where definitions of R1, R2, R3, R4 are the same as that above mentioned.
The definition of the sulfide is the same as that above mentioned.
The definitions of the solvent is the same as that above mentioned.
The definitions of the initiator is the same as that above mentioned.
The definitions of the reaction temperature is the same as that above mentioned.
The definitions of the reaction time is the same as that above mentioned.
A molar ratio of the initiator, the sulfide and a chiral β-amino substrate required for the reaction is that: initiator: sulfide: substrate is (0.01˜0.20): (0.01˜0.20):1.
In a fourth aspect, the present disclosure provides a method for racemizing ethyl 3β-amino-4-(2,4,5-trifluorophenyl) butyrate, obtained by racemizing (S)-3β-amino-4-(2,4,5-ethyl trifluorophenyl) butyrate under conditions of pentaerythritol tetra-3-mercaptopropionate (PETMP), azobisisobutyronitrile (AIBN) and toluene; wherein a reaction equation is:
The definitions of the reaction temperature is the same as that above mentioned.
The definitions of the reaction time is the same as that above mentioned.
A molar ratio of the initiator, the sulfide and a chiral β-amino substrate required for the reaction is that: initiator: sulfide: substrate is (0.01˜0.20): (0.01˜0.20):1.
The present disclosure provides a method for a racemic preparation of chiral β-amino acids of sitagliptin intermediate and derivatives thereof, the raw materials are convenient and easy to obtain, with low cost and high yield, the method is suitable for industrial production and preparation. Therefore, the technical solution provided by the present disclosure has high application value in industry.
In order to better understand the content of the present disclosure, further description will be given below in conjunction with specific embodiments, but the specific implementation is not a limitation on the content of the present disclosure.
(S)-3β-amino-4-(2,4,5-trifluorophenyl) methyl butyrate (4.94 g, 0.020 mol, ee>99%), toluene (20 ml), trimethylolpropane tris(3-mercaptopropionate) (TMMP, 160 mg, 0.40 mmol) and azobisisobutyronitrile (AIBN, 33 mg, 0.20 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 80° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 20 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (4.81 g, 0.0195 mol), which is the target product compound 1, with a yield of 97.4%; ee=0.78%. MS(ESI): m/z 248.0817[M+H]+.
(S)-3β-amino-4-(2,4,5-trifluorophenyl) ethyl butyrate (5.22 g, 0.020 mol, ee>99%), toluene (20 ml), pentaerythritol tetra-3-mercaptopropionate (PETMP, 98 mg, 0.20 mmol) and azobisisobutyronitrile (AIBN, 33 mg, 0.20 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 80° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 20 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (4.88 g, 0.0187 mol), which is the target product compound 2, with a yield of 93.5%; ee=0.65%. MS(ESI): m/z 262.0972[M+H]+.
(S)-3β-amino-4-(2,4,5-trifluorophenyl) isopropyl butyrate (5.51 g, 0.020 mol, ee>99%), toluene (20 ml), pentaerythritol tetra-3-mercaptopropionate (PETMP, 98 mg, 0.20 mmol) and azobisisobutyronitrile (AIBN, 33 mg, 0.20 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 80° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 20 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (5.07 g, 0.0184 mol), which is the target product compound 3, with a yield of 92%; ee=1.2%. MS(ESI): m/z 276.1128[M+H]+.
(S)-3β-amino-4-(2,4,5-trifluorophenyl) tert-butyl butyrate (5.79 g, 0.020 mol, ee>99%), toluene (30 ml), pentaerythritol tetra-3-mercaptopropionate (PETMP, 98 mg, 0.20 mmol) and azobisisobutyronitrile 33 mg, 0.20 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 80° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 20 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 5˜6 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (5.18 g, 0.0179 mol), which is the target product compound 4, with a yield of 89.5%; ee=1.9%. MS(ESI): m/z 290.1293[M+H]+.
(S)-3β-amino-1-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolone[4,3-a]pyrazine-7(8H)-4-(2,4,5-trifluorophenyl)butanone ((S)-sitagliptin, 8.15 g, 0.020 mol, ee>99%), toluene (30 ml), pentaerythritol tetra-3-mercaptopropionate (PETMP, 98 mg, 0.20 mmol) and azobisisobutyronitrile (AIBN, 33 mg, 0.20 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 80° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 22 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a white solid (7.13 g, 0.0175 mol), which is the target product compound 5, with a yield of 87.5%; ee=4%. MS(ESI): m/z 408.1179[M+H]+.
(R)-1-(2β-amino-4-(2,4-bis(trifluoromethyl)-5,8-dihydropyrido[3,4-D]pyrimidin-7(6H)-yl)-4-oxobutyl)-5,5-difluoropiperidin-2-one ((R)-gigliptin, 9.79 g, 0.020 mol, ee>99%), p-xylene (30 ml), trimethylolpropane tris(3-mercaptopropionate) (TMMP, 160 mg, 0.40 mmol) and azobisisoheptonitrile (ABVN, 50 mg, 0.20 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 70° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 22 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with ethyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (8.27 g, 0.0169 mol), which is the target product compound 6, with a yield of 84.5%; ee=1.6%. MS(ESI): m/z 490.1408[M+H]+.
(S)-4((S)-3β-amino-4-(2,4,5-trifluorophenyl)butyryl)-3-(tert-butyl methyl ether methyl) piperazin-2-one ((S)-itagliptin, 7.99 g, 0.020 mol, ee>99%), m-xylene (30 ml), pentaerythritol tetra-3-mercaptopropionate (PETMP, 98 mg, 0.20 mmol) and azobisisoheptonitrile (ABVN, 50 mg, 0.20 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 70° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 24 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with ethyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (6.78 g, 0.0170 mol), which is the target product compound 7, with a yield of 85%; ee=2.2%. MS(ESI): m/z 400.2137[M+H]+.
(S)-3β-amino-N-methyl-4-butanamide (2.32 g, 0.020 mol, ee>99%), dry benzene (20 ml), n-octyl mercaptan (0.29 g, 0.002 mol), azobisisobutyronitrile (AIBN, 66 mg, 0.40 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 60° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 20 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with ethyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (2.21 g, 0.0191 mol), which is the target product compound 8, with a yield of 95.3%; ee=2.4%. MS(ESI): m/z 117.0944[M+H]+.
(S)-3β-amino-N,N-dimethyl-4-butanamide (2.60 g, 0.020 mol, ee>99%), dimethyltetrahydrofuran (20 ml), dodecanethiol (0.41 g, 0.002 mol), azobisisobutyronitrile (AIBN, 66 mg, 0.40 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 60° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 20 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with ethyl acetate (2×20 ml).
The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (2.43 g, 0.0187 mol), which is the target product compound 9, with a yield of 95.3%; ee=2.7%. MS(ESI): m/z 131.1102[M+H]+.
(R)-3β-amino-3-phenyl-N-methyl-butyramide (3.56 g, 0.020 mol, ee>99%), toluene (20 ml), methyl thioglycolate (0.42 g, 0.004 mol), azobisisobutyronitrile (AIBN, 66 mg, 0.40 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 80° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 22 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (3.25 g, 0.0183 mol), which is the target product compound 10, with a yield of 91.2%; ee=2.8%. MS(ESI): m/z 179.1114[M+H]+.
(R)-3β-amino-4-phenyl-N,N-dimethylbutanamide (4.12 g, 0.020 mol, ee>99%), benzene (20 ml), n-octyl mercaptan (0.29 g, 0.002 mol), azobisisobutyronitrile (AIBN, 66 mg, 0.40 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 80° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 22 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (3.61 g, 0.0175 mol), which is the target product compound 11, with a yield of 87.6%; ee=2.6%. MS(ESI): m/z 207.1413[M+H]+.
(R)-3β-amino-4-phenyl-1-piperidinyl butanone (4.97 g, 0.020 mol, ee>99%), toluene (20 ml), methyl thioglycolate (0.42 g, 4.0 mmol), azobisisobutyronitrile (AIBN, 66 mg, 0.4 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 80° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 20 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (4.23 g, 0.0170 mol), which is the target product compound 12, with a yield of 85.1%; ee=2.3%. MS(ESI): m/z 249.1517[M+H]+.
(S)-3-ethyl aminobutyrate (2.62 g, 0.020 mol, ee>99%), toluene (20 ml), methyl mercaptopropionate (0.49 g, 4.0 mmol), azobisisoheptanitrile (ABVN, 99 mg, 0.40 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 60° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 26 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (2.53 g, 0.0193 mol), which is the target product compound 13, with a yield of 96.6%; ee=0.8%. MS(ESI): m/z 132.0951[M+H]+.
(R)-3β-aminobutyric acid (2.06 g, 0.020 mol, ee>99%), tetrahydrofuran (20 ml), water (2 mL), mercaptopropyltrimethoxysilane (0.79 g, 4.0 mmol), azobis isobutyronitrile (AIBN, 66 mg, 0.40 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 60° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 24 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 2-3 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to about 4.5 with 2N sodium hydroxide solution, a solid is precipitated, filtered to obtain a white viscous solid (1.55 g, 0.0150 mol), which is the target product compound 14, with a yield of 75.2%; ee=5.9%. MS(ESI): m/z 104.0631[M+H]+.
(R)-3β-amino-3-phenylpropionic acid (3.31 g, 0.020 mol, ee>99%), tetrahydrofuran (20 ml), mercaptopropyltrimethoxysilane (0.79 g, 4.0 mmol), azobis isobutyronitrile (AIBN, 66 mg, 0.40 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 60° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 24 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 2-3 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to about 4.5 with 2N sodium hydroxide solution, a solid is precipitated, filtered to obtain a white crystal (2.60 g, 0.0157 mol), which is the target product compound 15, with a yield of 78.5%; ee=6.2%. MS(ESI): m/z 166.0787[M+H]+.
(S)-4β-amino-2-pentanone (2.02 g, 0.020 mol, ee>99%), dry TOL (20 ml), pentaerythritol tetra-3-mercaptopropionate (PETMP, 98 mg, 0.20 mmol), azobisisobutyronitrile (AIBN, 33 mg, 0.20 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 80° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 26 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (1.87 g, 0.0185 mol), which is the target product compound 16, with a yield of 92.6%; ee=1.8%. MS(ESI): m/z 102.0847[M+H]+.
(R)-4β-amino-4-phenyl-2-butanone (3.26 g, 0.020 mol, ee>99%), dry TOL (20 ml), pentaerythritol tetra-3-mercaptopropionate (PETMP, 98 mg, 0.20 mmol), azobisisobutyronitrile (AIBN, 33 mg, 0.20 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 100° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 20 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (3.17 g, 0.0194 mol), which is the target product compound 17, with a yield of 97.2%; ee=1.5%. MS(ESI): m/z 164.0995 [M+H]+.
(S)-3β-amino-1,3-diphenyl-1-one (4.51 g, 0.020 mol, ee>99%), toluene (20 ml), pentaerythritol tetra-3-mercaptopropionate (PETMP, 98 mg, 0.20 mmol), azobisisobutyronitrile (AIBN, 33 mg, 0.20 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 120° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 18 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (4.41 g, 0.0196 mol), which is the target product compound 18, with a yield of 97.8%; ee=1.3%. MS(ESI): m/z 226.1157[M+H]+.
(S)-3-methylamino-4-(2,4,5-trifluorophenyl) butyric acid methyl ester (5.22 g, 0.020 mol, ee>99%), pentaerythritol tetra-3-mercaptopropionate (PETMP, 0.30 g, 0.60 mmol), azobisisobutyronitrile (AIBN, 66 mg, 0.40 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 80° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 20 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (4.87 g, 0.0187 mol), which is the target product compound 19, with a yield of 93.3%; ee=4.8%. MS(ESI): m/z 262.0973[M+H]+.
(R)-3β-amino-butyric acid methyl ester (3.87 g, 0.020 mol, ee>99%), toluene (20 ml), pentaerythritol tetra-3-mercaptopropionate (PETMP, 0.49 g, 0.010 mol), azodiisobutyronitrile (AIBN, 66 mg, 0.40 mmol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 100° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 22 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phases is combined, washed once with saturated brine (20 ml), dried with anhydrous sodium sulfate (10 g), filtered, and the filtrate is concentrated to dryness under reduced pressure at 35˜40° C. to obtain a colorless oil (3.54 g, 0.0183 mol), which is the target product compound 20, with a yield of 91.5%; ee=9.7%. MS(ESI): m/z 194.1108 [M+H]+.
(S)-3-methyl acetaminobutyrate (3.18 g, 0.020 mol, ee>99%), toluene (20 ml), pentaerythritol tetra-3-mercaptopropionate (PETMP, 0.98 g, 0.002 mol), azodiisobutyronitrile (AIBN, 0.17 g, 0.002 mol) are put into a 100 ml of three-necked flask, magnetic stirring is turned on. Under nitrogen protection, the temperature rises slowly to 120° C., the progress of the reaction is tracked by HPLC, and the reaction is complete after 24 h. 20 mL of water is added to the reaction solution, the pH value is adjusted to 4˜5 with 2N dilute hydrochloric acid, the liquids are separated, the organic phase is discarded. The pH value of the water phase is adjusted to 9˜10 with 2N sodium hydroxide solution, and extracting is performed twice with isopropyl acetate (2×20 ml). The organic phase is concentrated to dryness under reduced pressure, and separated by fast column chromatography to obtain a colorless oil (2.46 g, 0.0155 mol), which is the target product compound 21, with a yield of 77.3%; ee=16.5%. MS(ESI): m/z 160.0897[M+H]+.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201910705432.5 | Aug 2019 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2020/094818 | 6/8/2020 | WO |
