Allyl amines preparation

The reaction of an azide[185,186] or a trimethylsilylazide(I87] followed by the treatment with Ph3P is another preparative method for the primary allylic amine 307. 

Hydroxylysine (328) was synthesized by chemoselective reaction of (Z)-4-acet-oxy-2-butenyl methyl carbonate (325) with two different nucleophiles first with At,(9-Boc-protected hydroxylamine (326) under neutral conditions and then with methyl (diphenylmethyleneamino)acetate (327) in the presence of BSA[202]. The primary allylic amine 331 is prepared by the highly selective monoallylation of 4,4 -dimethoxybenzhydrylamine (329). Deprotection of the allylated secondary amine 330 with 80% formic acid affords the primary ally-lamine 331. The reaction was applied to the total synthesis of gabaculine 332(203]. 

Allylic amines can be cleaved. Hydrogenolysis of allylic amines of different stereochemistry with NaBH CN was applied to the preparation of both dia-stereoisomers 655 and 657 of cyclopentenylglycine from the cyclic amines 654 and 656 of different stereochemistry[405]. 

Aromatic enamines were prepared by dehydroha logenation of /3-bromo-amines with strong base. While trans enamines were thus formed, one obtained mostly cis enamines from rearrangement of the corresponding allylic amines under similar reaction conditions (646). Vicinal endiamines were obtained from S-dichloroamines and lithium amides (647). 

The isomerization of an allylic amine to an enamine by means of a formal 1,3-hydrogen shift constitutes a relatively small structural change. However, this transformation could be extremely valuable if it could be rendered stereoselective. In important early studies, Otsuka and Tani showed that a chiral cobalt catalyst, prepared in situ from a Co(ii) salt, a chiral phosphine, and diisobutylaluminum hydride (Dibal-H), can bring about the conversion of certain pro-chiral olefins to chiral, isomeric olefins by double bond migra-... 

The unsaturated oximes 224 (see Table 21) were readily prepared by AT-alkyl-ation of allyl amines with a-bromoketones or O-silyl-a-bromoaldoximes. Heating the oximes 224 in toluene under an argon atm at 110 -180 °C smoothly led to isoxazolidines 225 in good yields with cis ring junction stereochemistry. Even when three stereocenters were generated, as in 225 g-1, a single stereoisomer... 

Anderson CE, Overman LE (2003) Catalytic asymmetric rearrangement of allylic trichlor-oacetimidates. A practical method for preparing allylic amines and congeners of high enantiomeric purity. J Am Chem Soc 125 12412-12413... 

In addition, oxa-bridged pyrrolopyrimidines can be prepared by employing electron-poor allyl amines, with aldehydes and isocyanoacetamides [57]. The products can be transformed into the pyrrolopyridines by adding TFA at -78 °C to the reaction mixture. 

For the synthesis of heterocycles, an efficient strategy has been introduced utilizing the dual transition metal sequences (Scheme 6).11,lla The key issue is the compatibility of the two catalyst systems. Jeong et al. studied the one-pot preparation of bicyclopentenone 35 from propargylsulfonamide 33 and allylic acetate.11 This transformation includes two reactions the first palladium-catalyzed allylation of 33 generates an enyne 34 and the following Pauson-Khand type reaction (PKR) of 34 yields a bicyclopentenone 35. The success of this transformation reflects the right combination of catalysts which are compatible with each other because the allylic amination can be facilitated by the electron-rich palladium(O) catalyst and the PKR needs a Lewis-acidic catalyst. Trost et al. reported the one-pot enantioselective... 

Isomerization of allylic amines is another example of the application of the BINAP complex. Rh BINAP complex catalyzes the isomerization of N,N-diethylnerylamine 40 generated from myrcene 39 with 76-96% optical yield. Compound (R)-citronellal (R)-42. prepared through hydrolysis of (R)-41, is then cyclized by zinc bromide treatment.49 Catalytic hydrogenation then completes the synthesis of (—)-menthol. This enantioselective catalysis allows the annual production of about 1500 tons of menthol and other terpenic substances by Takasago International Corporation.50... 

Radical cyclization of N-alkenylamino acid derivatives Proline derivatives can be obtained by cyclization of N-alkenyl amino acid derivatives. Thus the (3-iodo allylic amine 2, prepared in 54% yield from threonine, cyclizes in the presence... 

Monomer Preparation, my]. Balsamic ftci-fl—Allyl amine (84.4 g 1.481 mol) in 100 mL of dichloromethane was added dropwise to recrystallized maleic anhydride (132 g 1.348 mol) in 500 mL of dichloromethane at room temperature. The reaction mixture was stirred for 2 hr at room temperature and then filtered to obtain 206 g (99% of theory) of pale yellow crystals, m.p. 110-112°C. 

Protected primary allylic amines are prepared from allyl halides and di-r-butyl imidodicarbonate 179 in the presence of lithium iodide, followed by the selective removal of one of the protecting groups by means of trifluoroacetic acid, e.g. equation 66187. 

Secondary allylic amines 184 have been prepared from aldehydes 181 (R1 = H, Me or Ph R2 = Me, Et or H) by the following sequence treatment with an amine R3NH2 (R3 = i-Pr, t-Bu, cyclohexyl or PhCH2) yields an imine 182, which is chlorinated by N-chlorosuccinimide. Dehydrochlorination of the resulting chloro compound with potassium t-butoxide gives an allylic imine 183, which is reduced to the product by means of methanolic sodium borohydride191. 

The silylated tin compound 199, obtained from tributyltin hydride and N-bis(trimethylsilyl)propargylamine (198) in the presence of a trace of AIBN (2,2/-azobisisobutyronitrile), is a versatile reagent for the preparation of allylic amines. Treatment with aryl bromides ArBr (Ar = Ph, 4-MeOCgH4, 4-O2NC6H4 etc.) under Pd(PPh3)4 catalysis yields the silylated amines 200, which are hydrolysed by acids to the free amines 201. 199 is converted into the lithium compound 202, which is transformed into 203 by aqueous ammonium chloride and into 204 by the action of alkyl halides RX (R = Me, Et or allyl) (equation 76)204. 

Amino alkenols have been prepared by palladium-catalyzed chloroacetoxylation and allylic amination of 1,3-dienes. 1,4-Acetoxychlorination is stereospecific and cyclic dienes give an overall cis- 1,4-addition12. Acetoxychlorination of 6-acetoxy-l,3-cycloheptadiene afforded only one isomer as shown in equation 8. Sequential substitution of the allylic chloro group can occur with either retention or inversion, thereby allowing complete control of the 1,4-relative stereochemistry (equation 9). 

Using a similar approach, l-acetoxy-4-diethylamino-2-butene and l-acetoxy-4-benzylamino-2-butene were prepared. Treatment of 1,3-butadiene with LiCl-LiOAc in the presence of Pd(OAc)2 and p-benzoquinone in acetic acid gave 91% l-acetoxy-4-chloro-2-butene (E/Z = 90/10). Subsequent allylic amination with diethylamine, catalyzed by Pd(PPh3)4 in THF, produced mainly ( )-l-acetoxy-4-diethylamino-2-butene13. 

Scheme 10.8 outlines the application of rhodium-catalyzed allyhc amination to the preparation of (il)-homophenylalanine (J )-38, a component of numerous biologically active agents [36]. The enantiospecific rhodium-catalyzed allylic amination of (l )-35 with the lithium anion of N-benzyl-2-nitrobenzenesulfonamide furmshed aUylamine (R)-36 in 87% yield (2° 1° = 55 1 >99% cee) [37]. The N-2-nitrobenzenesulfonamide was employed to facilitate its removal under mild reaction conditions. Hence, oxidative cleavage of the alkene (R)-36 followed by deprotection furnished the amino ester R)-37 [37, 38]. Hydrogenation of the hydrochloride salt of (l )-37 followed by acid-catalyzed hydrolysis of the ester afforded (i )-homophenylalanine (R)-3S in 97% overall yield. 

In a similar fashion, one of the halogens in quinoxaline 210 was displaced with allyl amines 211 in order to prepare intermediates 212 <99JOC8425>. These... 

Using catalyst 1, Blechert and co-workers were able to demonstrate the first sterically controlled CM reaction for the exclusive preparation of -olefms (Scheme 6). The best results were obtained using various substituted allylic amines, where the completely stereocontrolled installation of allylsilanes was observed. The mild conditions employed in these examples are noteworthy, as minimal racemization occurred when highly epimerizable chiral allyl amino esters were employed. 

Scheme 5). Whereas 5-substituted metallacycles 18 (R1 = Me, Ph) are quite unreactive, derivative 18 (R1 = H R2 = Ph), which is more efficiently prepared from the corresponding allyl amine 19 (R2 = Ph), allows insertion of tert-butyl isocyanide to furnish metallacycle 20 its metha-nolysis yielded a mixture of N- phenyl 21 and N-ferf-butylpyrrole 22. 

This procedure illustrates a general method for the preparation of rearranged allylic amines from allylic alcohols.2,3 The method is experimentally simple and has been used to prepare a variety of allylic prim-, sec-, and tert-carbonyl amines as illustrated in Table I. The only limitation encountered so far is a competing ionic elimination reaction which becomes important for tri-chloroacetimidic esters of 3-substituted-2-cyclohexen-l-ols.3 4 The rearrangement is formulated as a concerted [3,3]-sigmatropic rearrangement on the basis of its stereo- and regiospecificity3,5 which are... 

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