Enantioselective synthesis of tetrahydroquinoline alkaloids (-)-angustureine and (-)-cuspareine from chiral tert-butanesulfinyl imines

Article abstract of DOI:10.3987/COM-13-S(S)75

The addition of a Grignard reagent to both enantiomeric N-tert-butanesulfinyl imines derived from 3-(2-bromophenyl)propanal 8 proceeded with high diastereoselectivity. The resulting sulfinamides 9 and 12 were easily transformed into tetrahydroquinoline alkaloids (-)-angustureine (4) and (-)-cuspareine (5) after three steps: N-desulfinylation, intramolecular N-arylation and N-methylation.

Full text of DOI:10.3987/COM-13-S(S)75

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HETEROCYCLES, Vol. 88, No. 2, 2014, pp. 1163 - 1174. © 2014 The Japan Institute of Heterocyclic Chemistry
Received, 1st July, 2013, Accepted, 31st July, 2013, Published online, 1st August, 2013
DOI: 10.3987/COM-13-S(S)75
ENANTIOSELECTIVE SYNTHESIS OF TETRAHYDROQUINOLINE
ALKALOIDS (-)-ANGUSTUREINE AND (-)-CUSPAREINE FROM
CHIRAL tert-BUTANESULFINYL IMINES
Juan A. Sirvent, Francisco Foubelo,* and Miguel Yus*
Department of Organic Chemistry, Faculty of Science, and Institute of Organic
Synthesis (ISO), University of Alicante, Apdo. 99, 03080 Alicante, Spain
Abstract – The addition of a Grignard reagent to both enantiomeric
N-tert-butanesulfinyl imines derived from 3-(2-bromophenyl)propanal
8
proceeded with high diastereoselectivity. The resulting sulfinamides 9 and 12
were easily transformed into tetrahydroquinoline alkaloids (-)-angustureine (4)
and (-)-cuspareine (5) after three steps: N-desulfinylation, intramolecular
N-arylation and N-methylation.
INTRODUCTION
The enantioselective synthesis of 2-substituted tetrahydroquinolines has attracted much attention among
organic chemists because they are widespread subunits in natural alkaloids and pharmaceuticals as well.
For instance, simple synthetic 1,2,3,4-tetrahydroquinolines with interesting biological properties includes
oxamniquine (1), which has been used to combat parasitic disease schistosomiasis,1 the novel antibiotic
virantmycin (2),2 and the tetrahydroquinoline L-689,560 (3),3 one of the most potent NMDAR (N-methyl
d-aspartate receptor) antagonists yet described (Figure 1). On the other hand, among natural alkaloids,
(-)-angustureine (4), (-)-cuspareine (5), (-)-galipeine (6) and (-)-galipinine (7) were isolated from Galipea
officinalis Hancock (Figure 1),4 a Venezuelan shrubby tree used in folk medicine as tonic in dyspepsia,
dysentery, chronic diarrhea and also as antipyretic.5 The majority of the enantioselective synthesis of
these tetrahydroquinolines reported until today are based on asymmetric catalytic hydrogenation of the
corresponding quinolines.6 Other recent synthesis of (-)-angustureine (4) and (-)-cuspareine (5) included
as key steps a highly regio- and enantioselective intermolecular iridium-catalyzed allylic amination,7 the
conjugate addition of lithium (R)-N-phenyl-N-(-methylbenzyl)amide to an ,β-unsaturated
_____________________________________________________________________________________
This paper is dedicated to Professor Victor Snieckus on occasion of his 77th birthday.

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Figure 1
4-methoxyphenyl ester8 and the alkynylation of a chiral cyclic -amino ester.9 Interestingly, Wang and
co-workers provided also a synthesis of (+)-angustureine and (-)-cuspareine (5) involving a highly
diastereoselective addition of an alkynylmagnesium chloride to a (RS)-tert-butanesulfinyl imine as a key
step.10 Continuing our interest in the use of N-tert-butanesulfinyl imines11 as electrophiles, we envisioned
a straightforward synthesis of (-)-angustureine (4) and (-)-cuspareine (5), based on the diastereoselective
addition of Grignard reagents to these chiral imines,12 which have found high applicability in synthesis
because both enantiomers are accessible in large-scale processes13 and because the chiral auxiliary is
easily removed under acidic conditions. In addition, practical processes for recycling the
tert-butanesulfinyl group upon deprotection of N-tert-butanesulfinyl amines have also been reported.14 In
our synthetic strategy, similar to that provided by Wang,10 a palladium-catalyzed intramolecular
N-arylation will be also involved (Scheme 1).
Scheme 1
RESULTS AND DISCUSSION
As depicted in Scheme 1, our synthesis commenced with the diastereoselective addition of the
corresponding Grignard reagent to (E)-N-[3-(2-bromophenyl)propylydene]-tert-butanesulfinamide (8).
Chiral imines 8 were easily accessible from the corresponding tert-butanesulfinamide and

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3-(2-bromophenyl)propanal (obtained from commercially available 1,2-bromoiodobenzene and allylic
alcohol through a type-Heck coupling reaction).15 Ellman and co-workers reported for the first time the
addition of Grignard reagents to N-tert-butanesulfinyl aldimines.16 Interestingly, they found a marked
solvent effect on the stereoselectivity of the addition, no coordinating solvents, such as dichloromethane,
leading to the best results.17 In addition, and considering the configuration of the resulting diastereomers,
a chelated transition state I was proposed, which was also consistent with the observed solvent effect
(competitive coordination of ethereal solvents such as THF would interfere with the formation of the
six-membered-ring transition state). According to this model, the attack of the Grignard reagent occurred
on the Re face of the imine with the S configuration at the sulfur atom (Scheme 2). For that reason, we
studied first the addition of 1M solution of pentylmagnesium bromide in ether to the imine (S)-8 in
different solvents (Scheme 2). The addition was carried out at -78 ºC, and after that the reaction mixture
was allowed to reach room temperature. The highest diastereoselectivity was obtained performing the
reaction in toluene (94:6 dr), although similar levels of diastereocontrol were achieved using
dichloromethane and diethyl ether (92:8 and 93:7 dr, respectively). As it could be anticipated, the lowest
diastereoselectivity was reached in THF as solvent. The diastereomeric ratios were easily determined by
1H-NMR analysis of the crude reaction mixtures through the comparison of the integrals of the t-Bu
group and the N–H for each of the diastereoisomer (the largest chemical shift difference was always
observed for the diastereomeric signals of the N–H). In all cases complete conversion was observed using
two equivalents of the Grignard reagent, giving rise to the expected product 9 with R configuration at the
newly created stereogenic center (Scheme 2).
Scheme 2

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Free amine 10 was generated in quantitative yield from sulfinamide 9 upon reaction with 6M HCl in THF
at room temperature. Intramolecular N-arylation to produce the tetrahydroquinoline derivative 11 was
achieved in 81% yield under palladium catalysis, using Cs2CO3 as a base in toluene in a high pressure
tube at 115 ºC for 20 hours.15,18 Finally, N-methylation of 11 was achieved with paraformaldehyde and
sodium cyanoborohydride leading to (-)-angustureine (4) in 82% yield (Scheme 3).
Scheme 3
The same strategy was applied to the synthesis of (-)-cuspareine (5), starting in this case from the
enantiomeric aldimine (R)-8, since the configuration at the C2 position of the tetrahydroquinoline unit is
the opposite to that of the (-)-angustureine (4). The reaction of 1.5 equivalents of
2-(3,4-dimethoxyphenyl)ethylmagnesium bromide (prepared from the corresponding alkyl bromide and
magnesium in THF at 67 ºC) with aldimine (R)-8 in toluene proceeded in this case in moderate yield
(47%) and stereoselectivity (86:14 dr). Acidic hydrolysis of sulfonamide 12 led to free amine 13 in high
yield. Further palladium-catalyzed intramolecular N-arylation gave tetrahydroquinoline derivative 14 in
lower yield when comparing with the angustureine precursor shown above. Finally, methylation of 14
produced (-)-cuspareine (5) in 80% yield (Scheme 4).
In summary, 2-substituted tetrahydroquinoline alkaloids (-)-angustureine (4) and (-)-cuspareine (5) were
easily accessible from the imines derived from 3-(2-bromophenyl)propanal and (S)- or
(R)-tert-butanesulfinamide, respectively. The methodology presented here comprised as key steps a
diastereoselective addition of a Grignard reagent to a chiral sulfinyl imine, and a palladium-catalyzed
intramolecular N-arylation, following a strategy similar to that provided by Wang,10 without the need of

HETEROCYCLES, Vol. 88, No. 2, 2014
1167
sophisticated ligands for asymmetric metal catalyzed processes, which are required in other
stereoselective synthesis.6,7
Scheme 4
EXPERIMENTAL
All chemicals were commercially available (Acros, Aldrich). TLC was performed on Merck silica gel 60
F254, using aluminum plates and visualized with phosphomolybdic acid (PMA) stain. Chromatographic
purification was performed by flash chromatography using Merck silica gel 60 (0.040-0.063 mm) and
hexane/EtOAc as eluent. Low-resolution electron impact (EI) mass spectra were obtained at 70eV on
Agilent GC/MS-5973N apparatus equipped with a HP-5MS column (Agilent technologies, 30 m × 0.25
mm) and high resolution mass spectra (HRMS-ESI) were obtained on a Waters LCT Premier XE
apparatus equipped with a time of flight (TOF) analyzer and the samples were ionized by ESI techniques
and introduced through an ultra-high pressure liquid chromatograph (UPLC) model Waters ACQUITY H
CLASS. IR spectra were measured (film) with a Nicolet Impact 510 P-FT Spectrometer. NMR spectra

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were recorded with a Bruker AC-300 using CDCl3 as the solvent and TMS as internal standard. Optical
rotations were measured on a Perkin Elmer 341 polarimeter.
(3R,SS)-N-(tert-Butanesulfinyl)-1-(2-bromophenyl)octan-3-amine (9). To solution of aldimine (S)-8
(322 mg, 1.0 mmol) in dry toluene (4 mL) was added dropwise a 1M solution of pentylmagnesium
bromide in Et2O (2.0 mmol, 2.0 mL) at -78 ºC. The reaction was allowed to reach room temperature and
after 4 h, it was cooled down to 0 ºC, hydrolyzed with water (5 mL) and extracted with EtOAc (4 × 15
mL). The organic layers were successively washed with water (15 mL), brine (10 mL) and then dried over
magnesium sulfate and concentrate under vacuum (15 Torr). The residue was purified by column
chromatography (silica gel, hexane/EtOAc: 4/1) to yield 291 mg of pure product 9 (75% yield, 94:6 dr).
Physical and spectroscopic data follow: Yellow oil; []20D +28 (c 1.15, CH2Cl2); Rf 0.48 (hexane/EtOAc:
1/1); IR  (film) 1622, 1471, 1084, 1025, 749 cm-1; 1H NMR (300 MHz, CDCl3)  0.88 (3H, t, J = 6.8 Hz,
CH3), 1.25 [9H, s, (CH3)3], 1.27-1.47 (6H, m, CH2), 1.53-1.93 (4H, m, CH2), 2.70 (1H, ddd, J = 13.5,
11.1, 5.6 Hz, CH2), 2.90 (1H, ddd, J = 13.5, 11.1, 5.1 Hz, CH2), 3.08 (1H, br d, J = 6.9 Hz, NH),
3.24-3.37 (1H, m, CH), 7.02-7.09 (1H, m, ArH), 7.19-7.24 (2H, m, ArH), 7.52 (1H, d, J = 7.9 Hz, ArH);
13C NMR (75 MHz, CDCl3) 14.2 (CH3), 22.7 (CH2), 22.9 (CH3), 25.5 (CH2), 31.8 (CH2), 32.6 (CH2),
36.0 (CH2), 36.6 (CH2), 56.0 (C), 56.8 (CH), 124.4 (C), 127.7 (CH), 127.8 (CH), 130.4 (CH), 133.0
(CH), 141.5 (C); LRMS (EI) m/z 331 [M+ - 58 (81Br), 5%], 329 (5), 260 (7), 258 (7), 250 (24), 185 (33),
183 (33), 171 (46), 169 (48), 147 (100), 130 (19), 104 (29), 103 (17), 91 (31), 90 (17), 89 (10), 83 (14),
77 (28), 70 (11), 55 (10); HRMS (ESI) calcd for C18H31BrNOS (M+H) 388.1310, found 388.1302.
(3R)-1-(2-Bromophenyl)octan-3-amine (10). To solution of sulfinamide 9 (245 mg, 0.63 mmol) in THF
(1.5 mL) was added dropwise a 6M solution of HCl (0.6 mmol, 0.10 mL) at 0 ºC. The reaction mixture
was stirred at 20 ºC for 1 h. Then it was cooled down to 0 ºC and basified with 2M NaOH (1.0 mmol, 0.5
mL). The reaction mixture was extracted with EtOAc (3 × 15 mL), dried over magnesium sulfate, filtered
through a short pad of Celite and concentrated under vacuum (15 Torr) to give 177 mg of pure product 10
(99%). Physical and spectroscopic data follow: Yellow oil; []20 -6 (c 1.07, CH2Cl2); Rf 0.30
D
(CH2Cl2/methanol: 9/1); IR  (film) 2925, 1469, 1022, 747 cm-1; 1H NMR (300 MHz, CDCl3)  0.89 (3H,
t, J = 6.7 Hz, CH3), 1.20-1.40 (7H, m, CH2), 1.40-1.63 (2H, m, CH2), 1.67-1.90 (3H, m, CH2), 2.69-2.92
(3H, m, CH2, NH2), 6.99-7.09 (1H, m, ArH), 7.18-7.25 (2H, m, ArH), 7.52 (1H, d, J = 7.7 Hz, ArH); 13C
NMR (75 MHz, CDCl3)  14.2 (CH3), 22.8 (CH2), 25.9 (CH2), 32.1 (CH2), 33.0 (CH2), 38.0 (CH2), 38.3
(CH2), 51.2 (CH), 124.5 (C), 127.6 (2 x CH), 130.4 (CH), 132.9 (CH), 141.8 (C); LRMS (EI) m/z 284
[M+ (81Br), 1%], 282 (1), 214 (60), 212 (62), 204 (43), 171 (34), 169 (35), 100 (100); HRMS (ESI) calcd

HETEROCYCLES, Vol. 88, No. 2, 2014
1169
for C14H23BrN (M+H) 284.1014, found 284.1004.
(R)-2-Pentyltetrahydroquinoline (11).6a To a solution of amine 10 (152 mg, 0.53 mmol) in dry toluene
(5 mL) in a high pressure flask was successively added triphenylphosphine (21 mg, 0.081 mmol),
Pd(OAc)2 (6 mg, 0.027 mmol) and Cs2CO3 (345 mg, 1.06 mmol). The reaction mixture was stirred at 115
ºC for 20 h. The mixture was allowed to reach room temperature and hydrolyzed, first with 3M HCl (3.0
mmol, 1 mL) and then with 2M NaOH (8.0 mmol, 4 mL), and extracted with EtOAc (4 × 15 mL). The
organic layers were washed with brine (15 mL) and then dried over magnesium sulfate and concentrate
under vacuum (15 Torr). The residue was purified by column chromatography (silica gel, hexane/EtOAc:
20/1) to yield 87 mg of pure product 11 (81% yield). Physical and spectroscopic data follow: Colorless
oil; []20D +75 (c 1.10, CH2Cl2); Rf 0.44 (hexane/EtOAc: 16/1); IR  (film) 3400, 2925, 2853, 1606, 1483,
1
743 cm-1; H NMR (300 MHz, CDCl3)  0.90 ( 3H, t, J = 6.8 Hz, CH3), 1.25-1.52 (8H, m, CH2),
1.53-1.65 (1H, m, CH2), 1.95 (1H, dddd, J = 12.7, 5.5, 4.1, 3.0 Hz, CH2), 2.61-2.87 (2H, m, CH2), 3.22
(1H, dtd, J = 9.4, 6.2, 3.0 Hz, CH), 6.46 (1H, dd, J = 8.4, 1.2 Hz, ArH), 6.58 (1H, td, J = 7.4, 1.2 Hz,
13
ArH), 6.90-6.98 (2H, m, ArH); C NMR (75 MHz, CDCl3)  14.2 (CH3), 22.8 (CH2), 25.5 (CH2), 26.6
(CH2), 28.3 (CH2), 32.1 (CH2), 36.8 (CH2), 51.7 (CH), 114.2 (CH), 117.0 (CH), 121.5 (C), 126.8 (CH),
129.4 (CH), 144.9 (C); LRMS (EI) m/z 203 [M+ , 22%], 133 (13), 132 (100), 130 (11), 117 (11).
(-)-Angustureine [(R)-1-Methyl-2-pentyltetrahydroquinoline (4)]. To a solution of tetrahydroquinoline
11 (36 mg, 0.18 mmol) in acetonitrile (2 mL) in a 10 mL round-botton flask was successively added
paraformaldehyde (27 mg, 0.9 mmol), NaBH3CN (38 mg, 0.6 mmol) and acetic acid (0.034 mL, 0.6
mmol). The reaction mixture was stirred at 20 ºC for 15 h, then hydrolyzed with 2M NaOH (10.0 mmol, 5
mL), and extracted with EtOAc (4 × 15 mL). The organic layers were washed with brine (15 mL), then
dried over magnesium sulfate, and concentrate under vacuum (15 Torr). The residue was purified by
column chromatography (silica gel, hexane/EtOAc: 20/1) to yield 32 mg of pure product 4 (82% yield).
Physical and spectroscopic data follow: Colorless oil; []25D -6.8 (c 1.00, CHCl3) {lit.4a []25D -7.16 (c
1.00, CHCl3)}; Rf 0.18 (hexane); IR  (film) 2926, 1602, 1498, 741 cm-1; 1H NMR (300 MHz, CDCl3) 
0.89 (3H, t, J = 9.9 Hz, CH3), 1.20-1.45 (7H, m, CH2), 1.53-1.64 (1H, m, CH2), 1.83-1.92 (2H, m, CH2),
2.64 (1H, dt, J = 16.2, 4.2 Hz, CH2), 2.73-2.84 (1H, m, CH2), 2.91 (3H, s, CH3), 3.21 (1H, dq, J = 8.5, 4.2
Hz, CH), 6.51 (1H, d, J = 8.2 Hz, ArH), 6.57 (1H, td, J = 7.3, 1.0 Hz, ArH), 6.95 (1H, d, J = 7.3 Hz, ArH),
13
7.06 (1H, t, J = 7.7 Hz, ArH); C NMR (75 MHz, CDCl3)  14.2 (CH3), 22.8 (CH2), 23.7 (CH2), 24.6
(CH2), 25.9 (CH2), 31.4 (CH2), 32.2 (CH2), 38.1 (CH3), 59.1 (CH), 110.5 (CH), 115.3 (CH), 122.0 (C),
127.2 (CH), 128.7 (CH), 145.5 (C); LRMS (EI) m/z 217 [M+ (81Br), 14%], 147 (11), 146 (100), 144 (8).

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(3S,RS)-N-(tert-Butanesulfinyl)-1-(2-bromophenyl)-5-(3,4-dimethoxyphenyl)pentan-3-amine (12). To
solution of aldimine (R)-8 (632 mg, 2.0 mmol) in dry toluene (8 mL) was added dropwise a 0.5M solution
of 2-(3,4-dimethoxyphenyl)ethylmagnesium bromide in THF (3.0 mmol, 6.0 mL) at -78 ºC. The reaction
was allowed to reach room temperature and after 4 h, it was cooled down to 0 ºC and hydrolyzed with
water (5 mL), and extracted with EtOAc (4 × 15 mL). The organic layers were successively washed with
water (15 mL), brine (10 mL) and then dried over magnesium sulfate and concentrate under vacuum (15
Torr). The residue was purified by column chromatography (silica gel, hexane/EtOAc: 1/1) to yield 452
mg of pure product 12 (47% yield, 86:14 dr). Physical and spectroscopic data follow: Yellow oil; []20
D
-30 (c 0.99, CH2Cl2); Rf 0.27 (hexane/EtOAc: 1/2); IR  (film) 3262, 1515, 1261, 1235, 1024, 734 cm-1;
1H NMR (300 MHz, CDCl3)  1.24 [9H, s, (CH3)3], 1.71-1.85 (2H, m, CH2), 1.85-2.07 (3H, m, CH2),
2.65-2.76 (2H, m, CH2), 2.83-2.95 (1H, m, CH2), 3.14 (1H, br d, J = 7.1 Hz, NH), 3.29-3.38 (1H, m, CH),
3.85 (3H, s, CH3), 3.88 (3H, s, CH3), 6.69-6.80 (3H, m, ArH), 7.03-7.09 (1H, m, ArH), 7.17-7.26 (2H, m,
13
ArH), 7.52 (1H, dd, J = 8.0, 1.1 Hz, ArH); C NMR (75 MHz, CDCl3)  22.9 (CH3), 31.6 (CH2), 32.6
(CH2), 36.2 (CH2), 38.2 (CH2), 56.00 (CH3), 56.04 (CH3), 56.08 (C), 56.4 (CH), 111.4 (CH), 112.0 (CH),
120.4 (CH), 124.4 (C), 127.7 (CH), 127.9 (CH), 130.4 (CH), 133.0 (CH), 134.1 (C), 141.3 (C), 147.4 (C),
149.0 (C); LRMS (EI) m/z 425 [M+ - 58 (81Br), 33%], 423 (32), 376 (16), 374 (16), 261 (13), 259 (13),
197 (15), 195 (15), 192 (16), 171 (22), 169 (22), 165 (11), 164 (32), 152 (11), 151 (100), 132 (11), 117
(13), 107 (10), 91 (11), 77 (12); HRMS (ESI) calcd for C23H33BrNO3S (M+H) 482.1365, found 482.1351.
(3S)-1-(2-Bromophenyl)-5-(3,4-dimethoxyphenyl)pentan-3-amine (13). To solution of sulfinamide 12
(177 mg, 0.367 mmol) in THF (1.5 mL) was added dropwise a 6M solution of HCl (0.6 mmol, 0.10 mL)
at 0 ºC. The reaction mixture was stirred at 20 ºC for 1 h. Then it was cooled down to 0 ºC and basified
with 2M NaOH (1.0 mmol, 0.5 mL). The reaction mixture was extracted with EtOAc (3 × 15 mL), dried
over magnesium sulfate, filtered through a short pad of Celite, and concentrated under vacuum (15 Torr)
to give 137 mg of pure product 13 (99%). Physical and spectroscopic data follow: Yellow oil; []20
D
+3.1 (c 1.09, CH2Cl2); Rf 0.38 (CH2Cl2/methanol: 9/1); IR  (film) 2930, 1514, 1259, 1234, 1023, 748
cm-1; 1H NMR (300 MHz, CDCl3)  1.54-1.70 (2H, m, CH2), 1.70-1.92 (4H, m, CH2), 2.60 (1H, ddd, J =
13.8, 10.0, 6.1 Hz, CH2), 2.66-2.91 (4H, m, CH2, NH2), 3.85 (3H, s, CH3), 3.86 (3H, s, CH3), 6.71-6.75
(2H, m, ArH), 6.76-6.81 (1H, m, ArH), 7.00-7.08 (1H, m, ArH), 7.19-7.24 (2H, m, ArH), 7.52 (1H, d, J =
7.8 Hz, ArH); 13C NMR (75 MHz, CDCl3)  32.2 (CH2), 32.9 (CH2), 38.3 (CH2), 40.0 (CH2), 50.8 (CH),
55.9 (CH3), 56.0 (CH3), 111.4 (CH), 111.8 (CH), 120.2 (CH), 124.4 (C), 127.6 (CH), 127.7 (CH), 130.4
(CH), 132.9 (CH), 134.9 (C), 141.6 (C), 147.3 (C), 148.9 (C); LRMS (EI) m/z 379 [M+ (81Br), 2%], 377
(2), 362 (20), 360 (19), 298 (41), 214 (25), 212 (26), 177 (22), 171 (19), 169 (20), 152 (33), 151 (100);

HETEROCYCLES, Vol. 88, No. 2, 2014
1171
HRMS (ESI) calcd for C19H25BrNO2 (M+H) 378.1069, found 378.1066.
(S)-2-(3,4-Dimethoxyphenethyl)-1,2,3,4-tetrahydroquinoline (14).6h To a solution of amine 13 (124
mg, 0.328 mmol) in dry toluene (5 mL) in a high pressure flask was successively added
triphenylphosphine (19 mg, 0.073 mmol), Pd(OAc)2 (5.4 mg, 0.024 mmol) and Cs2CO3 (214 mg, 0.656
mmol). The reaction mixture was stirred at 115 ºC for 20 h. The mixture was left cooling to room
temperature and hydrolyzed, first with 3M HCl (3.0 mmol, 1 mL) and then with 2M NaOH (8.0 mmol, 4
mL), and extracted with EtOAc (4 × 15 mL). The organic layers were successively washed with brine (15
mL) and then dried over magnesium sulfate and concentrate under vacuum (15 Torr). The residue was
purified by column chromatography (silica gel, hexane/EtOAc: 20/1) to yield 44 mg of pure product 14
(45% yield). Physical and spectroscopic data follow: Yellow oil; []20D -37 (c 1.00, CH2Cl2); Rf 0.41
1
(hexane/EtOAc: 3/1); IR  (film) 3392, 2932, 1605, 1514, 1140, 1027, 745 cm-1; H NMR (300 MHz,
CDCl3)  1.59-1.74 (1H, m, CH2), 1.76-1.86 (2H, m, CH2), 1.99 (1H, dddd, J = 8.5, 5.5, 4.7, 2.4 Hz, CH2),
2.62-2.89 (4H, m, CH2), 3.30 (1H, dtd, J = 9.3, 6.3, 3.0 Hz, CH), 3.85 (3H, s, CH3), 3.87 (3H, s, CH3),
6.44 (1H, dd, J = 8.4, 1.1 Hz, ArH), 6.60 (1H, td, J = 7.4, 1.1 Hz, ArH), 6.71-6.83 (3H, m, ArH),
6.92-6.99 (2H, m, ArH); 13C NMR (75 MHz, CDCl3) 26.3 (CH2), 28.1 (CH2), 31.9 (CH2), 38.5 (CH2),
51.3 (CH), 56.0 (CH3), 56.1 (CH3), 111.4 (CH), 111.7 (CH), 114.2 (CH), 117.1 (CH), 120.2 (CH), 121.4
(C), 126.8 (CH), 129.3 (CH), 134.6 (C), 144.6 (C), 147.4 (C), 149.0 (C); LRMS (EI) m/z 297 (M+, 38%),
298 (8), 152 (7), 133 (11), 132 (100), 117 (8).
(-)-Cuspareine [(S)-2-(3,4-Dimethoxyphenethyl)-1-methyl-1,2,3,4-tetrahydroquinoline (5)]. To a
solution of tetrahydroquinoline 14 (30 mg, 0.10 mmol) in MeCN (1.2 mL) in a 10 mL round-botton flask
was successively added paraformaldehyde (27 mg, 0.9 mmol), NaBH3CN (38 mg, 0.6 mmol) and acetic
acid (0.034 mL, 0.6 mmol). The reaction mixture was stirred at 20 ºC for 15 h, then hydrolyzed with 2M
NaOH (10.0 mmol, 5 mL) and extracted with EtOAc (4 × 15 mL). The organic layers were washed with
brine (15 mL) and then dried over magnesium sulfate and concentrate under vacuum (15 Torr). The
residue was purified by column chromatography (silica gel, hexane/EtOAc: 20/1) to yield 25 mg of pure
product 5 (80% yield). Physical and spectroscopic data follow: Colorless oil; []25D -18.8 (c 1.00, CHCl3)
{lit.19 []25D -22.8 (c 1.00, CHCl3)}; Rf 0.50 (hexane/EtOAc: 3/1); IR  (film) 2932, 1498, 1260, 1233,
1
1028, 742 cm-1; H NMR (300 MHz, CDCl3)  1.67-1.79 (1H, m, CH2), 1.86-2.01 (3H, m, CH2), 2.53
(ddd, J = 13.9, 10.1, 6.5 Hz, CH2), 2.62-2.75 (2H, m, CH2), 2.79-2.90 (1H, m, CH2), 2.91 (3H, s, CH3),
3.28 (1H, td, J = 8.4, 4.2 Hz, CH), 3.85 (3H, s, CH3), 3.86 (3H, s, CH3), 6.53 (1H, d, J = 8.2 Hz, ArH),
6.56-6.62 (1H, m, ArH), 6.69-6.75 (2H, m, ArH), 6.79 (1H, d, J = 8.0 Hz, ArH), 6.98 (1H, d, J = 7.3 Hz,

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HETEROCYCLES, Vol. 88, No. 2, 2014
13
ArH), 7.08 (1H, t, J = 7.7 Hz, ArH); C NMR (75 MHz, CDCl3)  23.7 (CH2), 24.5 (CH2), 32.1 (CH2),
33.2 (CH2), 38.2 (CH3), 55.99 (CH3), 56.05 (CH3), 58.5 (CH), 110.7 (CH), 111.4 (CH), 111.7 (CH),
115.5 (CH), 120.2 (CH), 121.8 (C), 127.2 (CH), 128.8 (CH), 134.8 (C), 145.4 (C), 147.3 (C), 149.0 (C);
LRMS (EI) m/z 311 (M+, 25%), 147 (11), 146 (100).
ACKNOWLEDGEMENTS
This work was generously supported by the Spanish Ministerio de Ciencia e Innovación (Grant Nos.
CTQ2007-65218 and CTQ2011-24165, and Consolider Ingenio 2010-CSD-2007-00006), the Generalitat
Valenciana (Grant No. PROMETEO/2009/039 and FEDER) and the University of Alicante. J.A.S. thanks
the Spanish Ministerio de Ciencia e Innovación for a predoctoral fellowship. We also thank
MEDALCHEMY S.L. for a gift of chemicals.
REFERENCES
1. G. O. Kokwaro and G. Taylor, Drug Chem. Toxicol., 1990, 13, 347.
2. S. Omura and A. Nakagawa, Tetrahedron Lett., 1981, 22, 2199.
3. P. D. Leeson, R. W. Carling, K. W. Moore, A. M. Moseley, J. D. Smith, G. Stevenson, T. Chan, R.
Baker, A. C. Foster, S. Grimwood, J. A. Kemp, G. R. Marshall, and K. Hoogsteen, J. Med. Chem.,
1992, 35, 1954.
4. (a) I. Jacquemond-Collet, S. Hannedouche, N. Fabre, I. Fourasté, and C. Moulis, Phytochemistry,
1999, 51, 1167; (b) I. Jacquemond-Collet, F. Benoit-Vical, M. A. Valentin, E. Stanislas, M. Mallié,
and I. Fourasté, Planta Med., 2002, 68, 68.
5. P. J. Houghton, T. Z. Woldemariam, T. Watanabe, and M. Yates, Planta Med., 1999, 65, 250.
6. (a) W.-B. Wang, S.-M. Lu, P.-Y. Yang, X.-W. Han, and Y.-G. Zhou, J. Am. Chem. Soc., 2003, 125,
10536; (b) S.-M. Lu, Y.-Q. Wang, X.-W. Han, and Y.-G. Zhou, Angew. Chem. Int. Ed., 2006, 45,
2260; (c) W.-J. Tang, S.-F. Zhu, L.-J. Xu, Q.-L. Zhou, Q.-H. Fan, H.-F. Zhou, K. Lam, and A. S. C.
Chan, Chem. Commun., 2007, 613; (d) Z.-J. Wang, G.-J. Deng, Y. Li, Y.-M. He, W.-J. Tang, and
Q.-H. Fan, Org. Lett., 2007, 9, 1243; (e) C. Deport, M. Buchotte, K. Abecassis, H. Tadaoka, T. Ayad,
T. Ohshima, J.-P. Genet, K. Mashima, and V. Ratovelomanana-Vidal, Synlett, 2007, 2743; (f) D.-W.
Wang, W. Zeng, and Y.-G. Zhou, Tetrahedron: Asymmetry, 2007, 18, 1103; (g) M. Jahjah, M.
Alame, S. Pellet-Rostaing, and M. Lemaire, Tetrahedron: Asymmetry, 2007, 18, 2305; (h) X.-B.
Wang and Y.-G. Zhou, J. Org. Chem., 2008, 73, 5640; (i) F.-R. Gou, W. Li, X. Zhang, and Y.-M.
Liang, Adv. Synth. Catal., 2010, 352, 2441; (j) T. Wang, L.-G. Zhuo, Z. Li, F. Chen, Z. Ding, Y. He,
Q.-H. Fan, J. Xiang, Z.-X. Yu, and A. S. C. Chan, J. Am. Chem. Soc., 2011, 133, 9878.
7. (a) G. Satyanarayana, D. Pflästerer, and G. Helmchen, Eur. J. Org. Chem., 2011, 6877; (b) K.-Y. Ye,

HETEROCYCLES, Vol. 88, No. 2, 2014
1173
H. He, W.-B. Liu, L.-X. Dai, G. Helmchen, and S.-L. You, J. Am. Chem. Soc., 2011, 133, 19006.
8. S. A. Bentley, S. G. Davies, J. A. Lee, P. M. Roberts, and J. E. Thomson, Org. Lett., 2011, 13, 2544.
9. J. Tummatorn, G. Diaz Muñoz, and G. B. Dudley, Tetrahedron Lett., 2013, 54, 1312.
10. B.-L. Chen, B. Wang, and G.-Q. Lin, J. Org. Chem., 2010, 75, 941.
11. (a) F. Foubelo and M. Yus, Tetrahedron: Asymmetry, 2004, 15, 3823; (b) J. C. González-Gómez, F.
Foubelo, and M. Yus, Synlett, 2008, 2777; (c) M. Medjahdi, J. C. González-Gómez, F. Foubelo, and
M. Yus, Heterocycles, 2008, 76, 569; (d) M. Medjahdi, J. C. González-Gómez, F. Foubelo, and M.
Yus, J. Org. Chem., 2009, 74, 7859; (e) H. K. Dema, F. Foubelo, and M. Yus, Heterocycles, 2010,
80, 125; (f) J. C. González-Gómez, M. Medjahdi, F. Foubelo, and M. Yus, J. Org. Chem., 2010, 75,
6308; (g) H. K. Dema, F. Foubelo, and M. Yus, Heterocycles, 2011, 82, 1411; (h) M. Medjahdi, J. C.
González-Gómez, F. Foubelo, and M. Yus, Eur. J. Org. Chem., 2011, 2230; (i) H. K. Dema, F.
Foubelo, and M. Yus, Jordan J. Chem., 2011, 6, 247; (j) J. C. González-Gómez, F. Foubelo, and M.
Yus, Org. Synth., 2012, 89, 88; (k) I. Bosque, J. C. González-Gómez, F. Foubelo, and M. Yus, J.
Org. Chem., 2012, 77, 780 (correction: I. Bosque, J. C. González-Gómez, F. Foubelo, and M. Yus, J.
Org. Chem., 2012, 77, 4190); (l) I. Bosque, J. C. González-Gómez, A. Guijarro, F. Foubelo, and M.
Yus, J. Org. Chem., 2012, 77, 10340; (m) J. A. Sirvent, F. Foubelo, and M. Yus, Chem. Commun.,
2012, 48, 2543; (n) H. K. Dema, F. Foubelo, and M. Yus, Helv. Chim. Acta, 2012, 95, 1790; (o) M.
Medjahdi, J. C. González-Gómez, F. Foubelo, and M. Yus, Heterocycles, 2012, 86, 727; (q) M. J.
García-Muñoz, F. Foubelo, and M. Yus, Eur. J. Org. Chem., 2013, 1287; (r) J. A. Sirvent, F.
Foubelo, and M. Yus, Eur. J. Org. Chem., 2013, 2461.
12. For reviews, see: (a) G.-Q. Lin, M.-H. Xu, Y.-W. Zhong, and X.-W. Sun, Acc. Chem. Res., 2008, 41,
831; (b) F. Ferreira, C. Botuha, F. Chemla, and A. Pérez-Luna, Chem. Soc. Rev., 2009, 38, 1162; (c)
M. A. T. Robak, M. A. Herbage, and J. A. Ellman, Chem. Rev., 2010, 110, 3600.
13. (a) D. J. Weix and J. A. Ellman, Org. Lett., 2003, 5, 1317; (b) D. J. Weix and J. A. Ellman, Org.
Synth., 2005, 82, 157.
14. (a) M. Wakayama and J. A. Ellman, J. Org. Chem., 2009, 74, 2646; (b) V. K. Aggarwal, N. Barbero,
E. M. McGarrigle, G. Mickle, R. Navas, J. R. Suárez, M. G. Unthank, and M. Yar, Tetrahedron Lett.,
2009, 50, 3482.
15. G. S. Lemen and J. P. Wolfe, Org. Lett., 2011, 13, 3218.
16. G. Liu, D. A. Cogan, and J. A. Ellman, J. Am. Chem. Soc., 1997, 119, 9913.
17. D. A. Cogan, G. Liu, and J. Ellman, Tetrahedron, 1999, 55, 8883.
18. For similar N-arylation examples, see: (a) M. Liu, J. Li, X. Xiao, Y. Xie, and Y. Shi, Chem.
Commun., 2013, 49, 1404; (b) T. Guo, R. Song, B.-H. Yuan, X.-Y. Chen, X.-W. Sun, and G.-Q. Lin,
Chem. Commun., 2013, 49, 5402.

1174
HETEROCYCLES, Vol. 88, No. 2, 2014
19. J. H. Rokotoson, N. Fabre, I. Jacquemond-Collet, S. Hannedouche, I. Fourasté, and C. Moulis,
Planta Med., 1998, 64, 762.