Continuous and convergent access to vicinyl amino alcohols †

Five active pharmaceutical ingredients (APIs) containing the vicinyl amino alcohol moiety were synthesized using a convergent chemical assembly system. The continuous system is composed of four flow reaction modules: biphasic oxidation, Corey–Chaykovsky epoxidation, phenol alkylation

The chemical synthesis of active pharmaceutical ingredients (APIs) is generally accomplished via a linear batch approach where a single process produces a single compound.3][4] Chemical assembly systems (CAS) 5 are based on telescoping sequential robust reaction units that are linked together in a non-iterative fashion.Multi-step syntheses of a wide range of compounds of similar 6 or unique 5 structural cores can be accessed in a divergent fashion (Fig. 1).Here, we report on the application of CAS to convergent syntheses, where two structural variations of a key epoxide intermediate can be trapped in an aminolysis reaction to produce two distinct classes of b-amino alcohols, including five APIs.
Aryl epoxides should be accessible via a one-to-two step oxidation/Corey-Chaykovsky process.Employing robust and selective biphasic alcohol-oxidation conditions we developed earlier, 5 the first transformation is readily achieved and thus a continuous Corey-Chaykovsky epoxidation needed to be developed.Using benzaldehyde as a model system, a 0.5 M toluene solution was  mixed with an aqueous solution of trimethylsulfonium iodide ((CH 3 ) 3 S(I)O), sodium hydroxide (NaOH), and a substoichiometric amount of phase transfer catalyst (tetrabutylammonium iodide (TBAI)).The resulting biphasic solution was passed through a 10 mL reactor held at 90 1C at a pressure of 2 bar.Clean conversions to styrene oxide were observed with (CH 3 ) 3 S(I)O and NaOH in excess (1.4-2 equiv., Table 1 entries 1-3) after 24 minutes.Shorter reaction times, temperature, and the absence of TBAI resulted in decreased conversion (entries 5-7).
Using optimized conditions (97%, entry 2), we next turned to the amine ring-opening.While epoxide opening traditionally employed Lewis acids (LA), the elevated pressures and temperatures during microwave 13 and flow 12 transformations allow for clean reactions without LA catalysts.We aimed to combine epoxidation and ring opening by modifying established flow conditions. 12Thus, the crude toluene solution containing styrene oxide was mixed with t BuNH 2 in toluene/ethanol (2 : 1).With three equivalents of amine, good conversion to the desired regioisomer was observed after 50 minutes at 150 1C (Table 2, entry 1).Increasing the amount of amine to seven equivalents resulted in the highest regioselectivity at essentially full conversion (entry 3).Decreasing both the temperature and time resulted in lower conversions (entries 4 and 5).No product resulting from the bis-alkylation of the amine was observed under these conditions.
Modules 2 and 3 were connected with the help of a modified Jensen liquid-liquid separator, 14 allowing for the toluene phase exiting the epoxidation to be used directly in the ring opening reaction.Thus, after a total residence time of 74 minutes, benzaldehyde was transformed into 2-(tert-butylamino)-1phenylethanol 3 in 57% yield following off-line crystallization.A range of haloarenes reacted with isopropyl or tert-butyl amine without intermediate purification using the modular set-up.Moderate to good yields of the desired regioisomer were observed following product crystallization (Fig. 3).Tulobuterol, a b 2 -adrenergic agonist used to treat asthma, 15 was targeted.After passing 2-chloro benzyl alcohol through modules 1, 2, and 3 -with separators between modules 1/2 and 2/3 -the API was obtained in 27% yield (Fig. 3).
A number of hypertension medications such as propranolol, alprenolol, and metoprolol 16 contain the aryloxy b-amino alcohol motif.These targets were selected to expand the scope of the modular flow synthesis of vicinyl amino alcohols.Typical phenol alkylations require a large excess of epichlorohydrin equivalents 17 in the presence of an inorganic base. 18However, homogeneous solutions would facilitate the development of a flow process.A biphasic solution, obtained by mixing aqueous sodium hydroxide solution with a phenol in neat epichlorohydrin, should provide the desired aryloxy epoxide (Table 3).
The sodium hydroxide solution (1.95 M, 1.3 equiv.) is combined with phenol in three equivalents of neat epichlorohydrin via a T-mixer and passed through a reactor (1 h reaction time at 35 1C).Two major alkylation products (10, 11) were observed in roughly a 2 : 1 ratio, with the desired epoxide 10 obtained in 56% (Table 3, entry 1).Addition of substoichiometric amounts of PTC resulted in an increased conversion of the intermediate halohydrin (11) into the desired product (entry 2).At a reaction temperature of 45 1C, 10 was obtained in 86% yield while no intermediate halohydrin was observed (entry 3).At higher temperatures, a diol was formed by sodium hydroxide mediated ring opening of the epoxide. 19Reducing the excess of epichlorohydrin to two equivalents (entry 5, final conditions) had no effect, while a further reduction of the reagent to one equivalent yielded sizable amounts  of dimer 12 (entry 6).Shortening the residence time in the reactor to 46 minutes resulted in incomplete conversion (entry 4).Using this method, chiral aryloxy epoxides can be generated efficiently.When enantiopure epichlorohydrin is reacted using the conditions described above, the reaction proceeds with 93.7% ee (Fig. 4).
Module 4 depends on the solubility of the intermediate aryloxide in the biphasic solution.1][22] Phenol was efficiently alkylated at 110 1C after 60 minutes when epichlorohydrin served as solvent (3.1 M, 2 equiv.).By mixing the resulting solution with aqueous NaOH at 45 1C, 84% of the desired epoxide could be obtained after only 30 minutes (Fig. 5). 19ith a reliable process for the procurement of epoxide 10 in hand, the aminolysis module was connected (Table 2).Alkyl epoxides proved more active than aryl epoxides such that the ring opening proceeded at lower temperatures and shorter reaction times (Table 4).The epoxide solution was converted in just 20 min when mixed with five equivalents of isopropylamine in ethanol at 120 1C (entry 4).The reaction proceeds efficiently at 100 1C, but requires longer residence times (entry 2).Only one regioisomer and no amine dialkylation product were observed.
Finally, modules 3 and 4 were combined to yield the final sequence.The biphasic solution exiting module 4 is mixed with toluene.The toluene phase is removed using a membrane-based separator 14 and directly fed into module 3. Amino alcohol 16 was obtained in 48% yield from phenol, following off-line crystallization (Fig. 6).Several active pharmaceutical ingredients were prepared based on a judicious choice of starting materials.Racemic and chiral aryloxy b-amino alcohols can be prepared including propranolol (17, 51%), 23 used to treat hypertension, 24 alprenolol (18, 42%), an angina pectoris medication, 25 and the hypertension drugs bupranolol (19, 69%), 26 as well as metoprolol (20, 69%).
Described is the development of a convergent chemical assembly system consisting of four modules that reliably produces aryl and aryloxy b-amino alcohols in good yields.Modular flow units include biphasic oxidations, 5 Corey-Chaykovsky epoxidations, aryloxy alkylations, and epoxide aminolysis. 12queous in-line workup using liquid-liquid extractors resulted in continuous processes without intermediate purification.
Starting from phenols or benzyl alcohols five active pharmaceutical ingredients for the treatment of hypertension, agina pectoris, and bronchiodilation were produced.Enantiopure aryloxy b-amino alcohols can be prepared by starting from R/S epichlorohydrin.

Fig. 1
Fig. 1 Comparison of concepts for the chemical synthesis of small molecules.

Fig. 2
Fig. 2 Convergent synthesis of aryl and aryloxy vicinyl amino alcohols via a concluding epoxide ring opening.

Fig. 3
Fig. 3 Aryl vicinyl amino alcohols produced by continuous synthesis.a Residence time of Corey-Chaykovsky reaction is 40 min.See ESI † for full experimental details.

Fig. 5 Table 4 a
Fig. 5 To accommodate water-soluble and insoluble phenoxides, two variants of module 4, were implemented.

Table 1
Optimization of Corey-Chykovsky reaction (module 2) in flow a Equivalents with respect to benzaldehyde.c Reaction run at 60 1C.BPR: back pressure regulator, LLS: liquid/liquid separator.For full experimental details, see ESI. b
a b As determined by 1 H NMR. BPR: back pressure regulator.

Table 3
Optimization of the phenol alkylation in flow a