A short and convenient synthesis of novel thienopyrazolodiazepine and thienopyrazoloxazepine skeletons via nitrilimine cycloaddition

Article abstract of DOI:10.3987/COM-10-11905

Silver carbonate treatment of 3-thenyl-substituted hydrazonoyl chloride (3) promoted the in situ generation of the corresponding nitrilimine (4) which constitute the key intermediate in the three step synthesis of both thieno[2,3-f]pyrazolo[1,5-a][ 1,4]diazepine and thieno[2,3-f]pyrazolo[1,5-a][1, 4]-oxazepine skeletons. The concurrent formation of unusual pyridazine derivatives arising from the electrophilic attack of a nitrilium cation to the carbon-carbon double bond is also discussed in some detail.

Full text of DOI:10.3987/COM-10-11905

HETEROCYCLES, Vol. 81, No. 4, 2010
955
HETEROCYCLES, Vol. 81, No. 4, 2010, pp. 955 - 964. © The Japan Institute of Heterocyclic Chemistry
Received, 11th January, 2010, Accepted, 10th February, 2010, Published online, 12th February, 2010
DOI: 10.3987/COM-10-11905
A
SHORT
AND
CONVENIENT
SYNTHESIS
OF
NOVEL
THIENOPYRAZOLODIAZEPINE AND THIENOPYRAZOLOXAZEPINE
SKELETONS VIA NITRILIMINE CYCLOADDITION
Giorgio Molteni* and Paola Del Buttero
Università degli Studi di Milano, Dipartimento di Chimica Organica e Industriale,
via Golgi 19, 20133 Milano, Italy
Abstract – Silver carbonate treatment of 3-thenyl-substituted hydrazonoyl
chloride (3) promoted the in situ generation of the corresponding nitrilimine (4)
which constitute the key intermediate in the three step synthesis of both
thieno[2,3-f]pyrazolo[1,5-a][1,4]diazepine and thieno[2,3-f]pyrazolo[1,5-a][1,4]-
oxazepine skeletons. The concurrent formation of unusual pyridazine derivatives
arising from the electrophilic attack of a nitrilium cation to the carbon-carbon
double bond is also discussed in some detail.
INTRODUCTION
Since the early days of modern 1,3-dipolar cycloaddition chemistry, after the rationale introduced by
Huisgen in the ‘60,1 it becomes clear that nitrilimine cycloaddition represent a versatile and powerful tool
in the construction of the pyrazole nucleus.2 Then, the synthesis of annulated pyrazoles from both the
inter-3 and the intramolecular4 cycloadditions of substituted nitrilimines disclosed the opportunity to
obtain 4,5-dihydropyrazole derivatives of relevance in organic synthesis,5 as well as some related
products which received interesting biological applications.6 For instance, benzodiazepines annulated to a
nitrogen-containing five-membered ring like Alprazolam7 and Estazolam8 occupy a prominent place as
drugs in the treatment of CNS disturbances. By replacing the benzenic ring of the benzodiazepine moiety
with the thiophene one, thienotriazolodiazepine skeletons are obtained. Among these latter substrates
Brotizolam9 and Etizolam10 belongs to a new class of diazepines which possesses amnesic, anxiolytic,
anticonvulsant, hypnotic, sedative and skeletal muscle relaxant properties.
In the present paper we undertook the investigation of intermolecular cycloadditions between
3-thenyl-substituted hydrazonoyl chloride (3) and simple monosubstituted dipolarophiles bearing a

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HETEROCYCLES, Vol. 81, No. 4, 2010
carbon-carbon double bond, namely allyl bromide and allyl alcohol, with the aim to synthesize the
already unreported thieno[2,3-f]pyrazolo[1,5-a][1,4]diazepine and thieno[2,3-f]pyrazolo[1,5-a][1,4]-
diazepine skeletons.
RESULTS AND DISCUSSION
Synthesis of thienopyrazolodiazepine and thienopyrazoloxazepine skeletons. 3-Thenyl-substituted
hydrazonoyl chloride (3) was readily prepared from the commercially available aminoester (1) by
diazotisation followed by coupling with ethyl 2-chloroacetoacetate (Scheme 1).
O
O
CO2Me
Cl
+
_
N
NH
NH2
CO2Me
N N Cl
OMe
NaNO2/HCl
0-5°C
Cl
CO2Me
CO2Me
S
S
S
1
2
3 (80%)
Scheme 1
The in situ generation of the labile nitrilimine intermediate (4) was accomplished by treating the
corresponding hydrazonoyl chloride (3) with a twofold molar excess of silver carbonate in ethyl acetate at
room temperature following a well-established procedure previously elaborated by Garanti and Zecchi.11
4,5-Dihydropyrazoles (5), (6) and the 1,4,5,6-tetrahydropyridazine derivative (7) were obtained (see
Scheme 2). The extent of the cycloaddition between hydrazonoyl chloride (3) and allyl bromide or allyl
alcohol was strongly dependent upon the chemical features of the dipolarophile. While allyl bromide gave
rise to the corresponding 4,5-dihydropyrazole (5) with 76% yield, allyl alcohol gave a mixture of the
desired cycloadduct (6) (23%) and the unusual 1,4,5,6-tetrahydropyridazine derivative (7) (69%) (vide
infra). The obtainment of 5-substituted-4,5-dihydropyrazoles (5) and (6) reflects the usual HOMO dipole
control of nitrilimine cycloadditions to monosubstituted ethylenes.12 In order to enhance the isolation
yield of 4,5-dihydropyrazole (6), two other cycloaddition conditions were exploited. Unfortunately, the
classic route carried out in the presence of a large excess of triethylamine in boiling toluene gave rise to
large amounts of tarry materials, while non-classical aqueous conditions13 performed in aqueous sodium
hydrogencarbonate as the reaction medium in the presence of tetrahexylammonium chloride as the
surfactant did not produce any appreciable result, since unreacted (3) was recovered.
As the final step of our synthesis, the 1,4-diazepine or 1,4-oxazepine ring closure from cycloadducts (5)
and (6), respectively, was carried out by internal nucleophilic attack. The required nucleophilic species
were generated by treating (5) with ammonia and (6) with potassium ter-butoxide. No intermediates were
isolated since spontaneous ring closure to tricyclic products (8) and (9) just occurred. By contrast, the

HETEROCYCLES, Vol. 81, No. 4, 2010
957
transformation (6) → (9) failed under acidic catalytic conditions (PTSA and PPA) since unreacted (6) was
always recovered. The structure of all new compounds (6)-(9) were firmly established by elemental
1
analyses and spectral data, including H and 13C-NMR, IR, and MS spectrometry (see Experimental
section). In particular, 1H-NMR spectra of target compounds (8) and (9) show a complex splitting pattern
(overlapping signals) due to the four protons bonded to the pyrazoline and the 1,4-diazepine rings. Upon
irradiation of the proton in the 5-position of the pyrazoline ring at 5.80 , two distinct AB systems appear
in the case of compound (8). The first one at 3.29  (J = 18.2 Hz) is due to the two protons in the
3-position of the pyrazoline ring, while the second (3.34 , J = 12.1 Hz) is related to the couple of protons
in the 3-position of the diazepine ring. These observed chemical shifts and scalar coupling constants are
in perfect agreement to literature values.14
_
+
CO2Me
N
N
Ag2CO3
AcOEt
3
CO2Me
S
4
OH
Br
MeO2C
N
CO2Me
CO2Me
N
N
N
N
N
+
Br
OH
CO2Me
OH
CO2Me
CO2Me
S
S
S
5 (76%)
6 (23%)
t-BuOK
7 (69%)
NH3/EtOH
NH4OH
CO2Me
CO2Me
N
N
N
N
NH
O
S
S
O
O
8 (83%)
9 (40%)
Scheme 2

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HETEROCYCLES, Vol. 81, No. 4, 2010
Formation of 1,4,5,6-tetrahydropyridazine derivatives. To this point, we perceived the opportunity to
study in some detail the formation of 1,4,5,6-tetrahydropyridazine derivatives quite similar to (7).
Although unusual, the formation of the 1,4,5,6-tetrahydropyridazine ring from the reaction between
hydrazonoyl chlorides and allyl alcohol is a documented matter15 and can be rationalised on the grounds
of the intermediates A-C depicted in the Scheme 3. Due to the ability of the silver ion to facilitate the
heterolysis of the carbon-halogen bond,16 it is reasonable to posit the initial formation of the nitrilium
cation A. Further evolution of A lead to nitrilimine intermediate (4), which give cycloadduct (6), and to
carbocation B. In the present case, pinacol-type rearrangement of the latter specie17 give carbonyl
derivatives C which cyclize to (7). It needs to be added that: (i) carbonyl derivatives quite similar to C
were really isolated by reacting the 2-methoxycarbonylphenyl-substituted hydrazonoyl chloride (10b in
the present paper) with but-3-en-2-ol and phenyl vinylcarbinol,15 and (ii) the intermediacy of carbocation
B as the precursor of both products (6) and (7) can be ruled out since the retention of stereochemistry in
the case of substituted allylic alkenols.15
Ag+
_
OH
+
+
CO2Me
CO2Me
R NH N
R N N
6
3
- H+
- AgCl
A
4
OH
CO2Me
+
CO2Me
1,2-H shift
- H+
R NH N
R NH N
7
OH
CHO
B
C
R =
CO2Me
S
Scheme 3
Hence, hydrazonoyl chlorides (10) were submitted to reaction with allyl alcohol in the presence of silver
carbonate (Scheme 4). Reaction output are summarised in Table 1 and show that product ratio (12) : (11)
enhances according to the steric encumbrance of substituent R. This finding implies that the substituent R
hinders the approach of nitrilimine (4) to the carbon-carbon double bond of allyl alcohol on parallel
planes, as requested for the concerted mechanism of nitrilimine cycloadditions.18 It is apparent that the
presence of bulky R made easier the attack of nitrilium cation A to allyl alcohol with respect to that of
nitrilimine (4). In fact, the approach of the electrophilic specie A to the carbon-carbon double bond does
not suffer from the rigorous geometrical constraints which works in dipolar cycloadditions.

HETEROCYCLES, Vol. 81, No. 4, 2010
959
CO2Me
OH
CO2Me
CO2Me
Cl
N
N
N
OH
NH N
R
N
+
Ag2CO3/AcOEt
1
R
1
R
1
R
R
R
OH
10
11
12
Scheme 4
Table 1. Reaction between hydrazonoyl chlorides (10) and allyl alcohol.
____________________________________________________________________________________
R
R1
Product yields (%)
Product ratio
(12) : (11)
_______________________________
(11)
(12)
____________________________________________________________________________________
__
H
Me
H
93
83
56
39
0
CO2Me
I
10
30
52
0.12
0.54
1.33
H
t-Bu
H
____________________________________________________________________________________
CONLUSIONS
The synthesis of the novel thieno[2,3-f]pyrazolo[1,5-a][1,4]diazepine and thieno[2,3-f]pyrazolo[1,5-a]-
[1,4]oxazepine skeletons of potential interest as pharmacophoric agents have been carried out by the
nitrilimine-alkene cycloaddition as the key step. Since the transformation (5) → (8) occur with 63%
overall yield, the present synthetic approach constitutes a reliable way to obtain the above
thienopyrazolodiazepine skeleton in the multi-gram scale. The occurrence of 1,4,5,6-tetrahydropyridazine
as unusual products of the reaction between hydrazonoyl chlorides and allyl alcohol have been
investigated by varying the size of the substituent R. An increase of the 1,4,5,6-tetrahydropyridazine yield
was experienced in the presence of bulky R indicating the geometrical freedom of electrophilic attack by
nitrilium cation A to the C=C bond with respect to concerted dipolar cycloaddition.
EXPERIMENTAL
Melting points were determined with a Büchi apparatus in open tubes and are uncorrected. IR spectra
were recorded with a Perkin-Elmer 1725 X spectrophotometer. MS spectra were determined with a
1
VG-70EQ apparatus. H-NMR (300 MHz) and 13C-NMR (75 MHz) spectra were taken with a Bruker
AMX 300 instrument (in CDCl3 solutions at room temperature). Chemical shifts are given as ppm from
tetramethylsilane and J values are given in Hz.
Hydrazonoyl chlorides (10a),19 (10b)15 and 4,5-dihydropyrazole derivatives (11a),20 (11b)15 are known in
the literature.

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HETEROCYCLES, Vol. 81, No. 4, 2010
Synthesis of hydrazonoyl chlorides (3) and (10). General procedure. A solution of 2-methoxy-
carbonyl-3-aminothiophene (1) or the appropriate aniline (15.0 mmol) in a mixture of water (25 mL) and
MeOH (15 mL) was treated with aqueous HCl (10 M, 4.5 mL) and then cooled to 0 °C. Sodium nitrite
(1.31 g, 19.0 mmol) was added portionwise to the cooled and stirred reaction mixture. After 15 min, the
cold mixture was adjusted to pH 5 with sodium acetate and then a solution of methyl 2-chloroacetoacetate
(2.34 g, 15.0 mmol) in MeOH (15 mL) was added with cooling and stirring of the mixture, which was
stirred overnight at room temperature and then extracted with CH2Cl2 (2 x 35 mL). The organic layer was
washed with aqueous sodium hydrogencarbonate (5%, 20 mL), dried over Na2SO4 and evaporated.
Recrystallisation from iPr2O gave the pure hydrazonoyl chlorides (3) or (10).
Hydrazonoyl chloride (3) (3.31 g, 80%) as pale yellow powder having mp 163-165 °C; IR (Nujol): 3250,
1735, 1690 (cm-1); 1H-NMR: 3.95 (3H, s), 3.97 (3H, s), 7.38 (1H, d, J = 5.4), 7.47 (1H, d, J = 5.4), 10.80
(1H, br s). MS: 276 m/z (M+). Anal. Calcd for C9H9ClN2O4S: C, 39.06; H, 3.28; N, 10.13. Found: C,
39.10, H, 3.31; N, 10.19.
Hydrazonoyl chloride (10c) (4.36 g, 86%) as yellow powder having mp 95-97 °C; IR (Nujol): 3270, 1735
(cm-1); 1H-NMR: 3.98 (3H, s), 6.84 (1H, td, J = 7.5, 1.6), 7.38 (1H, td, J = 7.5, 1.6), 7.60 (1H, dd, J = 8.4,
2.2), 7.76 (1H, dd, J = 8.4, 2.2), 8.81 (1H, br s). MS: 338 m/z (M+). Anal. Calcd for C9H8ClIN2O2: C,
31.91; H, 2.38; N, 8.28. Found: C, 31.96, H, 2.42; N, 8.33.
Hydrazonoyl chloride (10d) (3.62 g, 90%) as white powder having mp 67-69 °C; IR (Nujol): 3240, 1730
1
(cm-1); H-NMR: 0.94 (9H, s), 3.95 (3H, s), 6.89 (1H, td, J = 7.4, 1.8), 7.30 (1H, td, J = 7.4, 1.8), 7.51
(1H, dd, J = 8.5, 2.1), 7.70 (1H, dd, J = 8.5, 2.1), 8.80 (1H, br s). MS: 268 m/z (M+). Anal. Calcd for
C13H17ClN2O2: C, 58.08; H, 6.38; N, 10.43. Found: C, 58.11, H, 6.41; N, 10.50.
Cycloaddition between hydrazonoyl chloride (3) and allyl bromide.
A solution of hydrazonoyl chloride (3) (2.50 g, 9.1 mmol) and allyl bromide (3.30 g, 27.3 mmol) in
EtOAc (45 mL) was treated with silver carbonate (5.02 g, 18.2 mmol), and stirred in the dark at room
temperature for 48 h. The undissolved material was filtered off, the solvent was evaporated, and then the
residue was chromatographed on a silica gel column with hexane-EtOAc 7 : 3 giving 1-[(2-metoxy-
carbonyl)-3-thenyl]-3-methoxycarbonyl-5-bromomethyl-4,5-dihydropyrazole (5) (2.50 g, 76% yield) as
1
pale yellow powder having mp 152-154 °C (from iPr2O); IR (Nujol): 1715, 1700 (cm-1); H-NMR:
3.22-3.46 (4H, m), 3.89 (3H, s), 3.92 (3H, s), 5.80-5.90 (1H, m), 7.37 (1H, d, J = 5.4), 7.44 (1H, d, J =
5.4). After irradiation at 5.85 δ: 3.27 (1H, d, J = 18.1), 3.29 (1H, d, J = 11.0), 3.34 (1H, d, J = 18.1), 3.42
(1H, d, J = 11.0). 13C-NMR: 33.2 (t), 37.2 (t), 52.0 (q), 52.3 (q), 62.5 (d), 125.0 (d), 130.7 (d), 133.6 (s),
141.1 (s), 145.6 (s), 161.6 (s), 162.5 (s). MS: 361 m/z (M+). Anal. Calcd for C12H13BrN2O4S: C, 39.89; H,
3.63; N, 7.76. Found: C, 39.93, H, 3.67; N, 7.82.

HETEROCYCLES, Vol. 81, No. 4, 2010
961
Cycloaddition between hydrazonoyl chloride (3) and allyl alcohol.
A solution of the hydrazonoyl chloride (3) (2.48 g, 9.0 mmol) and allyl alcohol (2.61 g, 45.0 mmol) in
EtOAc (40 mL) was treated with silver carbonate (4.97 g, 18.0 mmol), and stirred in the dark at room
temperature for 64 h. The undissolved material was filtered off, the solvent was evaporated, and then the
residue was chromatographed on a silica gel column with hexane-EtOAc 10 : 3. First fractions contained
1-[(2-methoxycarbonyl)-3-thenyl]-3-methoxycarbonyl-6-hydroxy-1,4,5,6-tetrahydropyridazine (7) (1.85
g, 69% yield) as yellow powder having mp 120-122 °C (from iPr2O); IR (Nujol): 3450, 1720, 1690
1
(cm-1); H-NMR: 1.25-1.55 (1H, m), 2.14-2.21 (1H, m), 2.54-2.79 (2H, m), 3.84 (3H, s), 3.88 (3H, s),
5.32 (1H, dd, J = 8.4, 2.7), 5.60 (1H, br s), 7.11 (1H, d, J = 5.4), 7.39 (1H, d, J = 5.4). After addition of
D2O: 1.52 (1H, dddd, J = 9.8, 7.2, 6.2, 2.5), 2.14-2.21 (1H, m), 2.62 (1H, ddd, J = 18.4, 13.8, 6.6), 2.77
(1H, ddd, J = 18.4, 8.5, 6.0). 13C-NMR: 16.3 (t), 22.3 (t), 52.3 (q), 52.5 (q), 78.8 (d), 126.2 (d), 131.1 (d),
133.5 (s), 138.4 (s), 145.8 (s), 160.4 (s), 162.8 (s). MS: 298 m/z (M+). Anal. Calcd for C12H14N2O5S: C,
48.31; H, 4.73; N, 9.40. Found: C, 48.27, H, 4.69; N, 9.44.
Further elution with EtOAc gave 1-[(2-metoxycarbonyl)-3-thenyl]-3-methoxycarbonyl-5-hydroxymethyl-
4,5-dihydropyrazole (6) (0.62 g, 23% yield) as white powder having mp 132-134 °C (from iPr2O); IR
(Nujol): 3500, 1720, 1710 (cm-1); 1H-NMR: 3.65-3.70 (2H, m), 3.71 (1H, dd, J = 8.6, 2.0), 3.79 (1H, dd,
J = 8.6, 1.8) 3.80 (3H, s), 3.82 (3H, s), 4.84 (1H, br s), 5.23-5.31 (1H, m), 7.26 (1H, d, J = 5.4), 7.43 (1H,
d, J = 5.4). 13C-NMR: 34.7 (t), 52.1 (q), 52.2 (q), 61.9 (t), 65.2 (d), 125.0 (d), 130.8 (d), 133.6 (s), 140.3
(s), 144.7 (s), 160.8 (s), 162.2 (s). MS: 298 m/z (M+). Anal. Calcd for C12H14N2O5S: C, 48.31; H, 4.73; N,
9.40. Found: C, 48.36, H, 4.77; N, 9.46.
Cyclisation to thieno[2,3-f]pyrazolo[1,5-a][1,4]diazepine (8).
A solution of (5) (1.44 g, 4.0 mmol) in 2M ethanolic ammonia (40 mL, 80.0 mmol) and 30% aqueous
ammonium hydroxide (10 mL, 85.7 mmol) was stirred at room temperature for 48 h. Partial evaporation
of the solvent gave a residue that was extracted with CH2Cl2 (70 mL). The organic layer was dried over
Na2SO4, the solvent was removed under reduced pressure and the residue was crystallised with iPr2O
giving pure 2-oxo-6-methoxycarbonyl-4H-thieno[2,3-f]pyrazolo[1,5-a][1,4]diazepine (8) (0.88 g, 83%
yield) as white powder having mp 163-165 °C; IR (Nujol): 3430, 1730, 1690 (cm-1); 1H-NMR: 3.22-3.41
(4H, m), 3.85 (3H, s), 5.75-5.85 (1H, m), 7.16 (1H, d, J = 5.4), 7.28 (1H, br s), 7.40 (1H, d, J = 5.4). After
irradiation at 5.80 δ: 3.26 (1H, d, J = 18.2), 3.30 (1H, d, J = 12.1), 3.32 (1H, d, J = 18.2), 3.38 (1H, d, J =
13
12.1). C-NMR: 36.5 (t), 52.0 (q), 60.8 (t), 62.5 (d), 124.7 (d), 130.9 (d), 137.2 (s), 144.5 (s), 145.9 (s),
161.6 (s), 163.6 (s). MS: 265 m/z (M+). Anal. Calcd for C11H11N3O3S: C, 49.80; H, 4.18; N, 15.85. Found:
C, 49.75, H, 4.21; N, 15.92.

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HETEROCYCLES, Vol. 81, No. 4, 2010
Cyclisation to thieno[2,3-f]pyrazolo[1,5-a][1,4]oxazepine (9).
To a solution of (6) (1.31 g, 4.4 mmol) in anhydrous tetrahydrofuran (30 mL) under nitrogen atmosphere
was added potassium ter-butoxide (0.57 g, 5.1 mmol). The mixture was stirred at room temperature for 24
h. Evaporation of the solvent gave a residue that was taken up with water (25 mL) and then extracted with
CH2Cl2 (2 x 35 mL). The organic layer was dried over Na2SO4, the solvent was removed under reduced
pressure and the residue was chromatographed on a silica gel column with EtOAc. Subsequent
crystallisation with iPr2O gave pure 2-oxo-6-methoxycarbonyl-4H-thieno[2,3-f]pyrazolo[1,5-a][1,4]-
oxazepine (9) (0.47 g, 40%) as a white powder having mp 229-231 °C; IR (Nujol): 1720, 1690 (cm-1);
1H-NMR: 3.02 (1H, dd, J = 18.5, 10.8), 3.60 (1H, dd, J = 18.5, 12.8), 3.94 (3H, s), 4.49 (2H, m),
4.63-4.70 (1H, m), 7.32 (1H, d, J = 5.4), 7.62 (1H, d, J = 5.4). 13C-NMR: 34.1 (t), 52.6 (q), 63.1 (t), 68.6
(d), 120.2 (d), 128.8 (d), 130.8 (s), 135.4 (s), 143.1 (s), 160.8 (s), 162.4 (s). MS: 266 m/z (M+). Anal.
Calcd for C11H10N2O4S: C, 49.62; H, 3.79; N, 10.53. Found: C, 49.58, H, 3.76; N, 10.59.
Cycloaddition between hydrazonoyl chlorides (10) and allyl alcohol. General procedure.
A solution of the hydrazonoyl chloride (10) (8.0 mmol) and allyl alcohol (2.32 g, 40.0 mmol) in EtOAc
(40 mL) was treated with silver carbonate (4.41 g, 16.0 mmol), and stirred in the dark at room
temperature for 60 h. The undissolved material was filtered off, the solvent was evaporated, and then the
residue was chromatographed on a silica gel column with CH2Cl2-EtOAc 8 : 2. First fractions contained
tetrahydropyridazine derivatives (12), further elution gave dihydropyrazoles (11).
Dihydropyrazole (11c) (1.61 g, 56%) as pale yellow powder having mp 131-132 °C (from iPr2O); IR
(Nujol): 3450, 1730 (cm-1); 1H-NMR: 3.22 (1H, dd, J = 17.7, 8.8), 3.29 (1H, dd, J = 17.7, 10.9), 3.43 (1H,
dd, J = 11.9, 3.3), 3.47 (1H, dd, J = 11.9, 4.3), 3.83 (3H, s), 4.67 (1H, br s), 4.77-4.86 (1H, m), 6.95 (1H,
td, J = 7.6, 1.8), 7.31-7.34 (2H, m), 7.84 (1H, dd, J = 8.6, 2.1). 13C-NMR: 34.1 (t), 52.1 (q), 61.5 (t), 66.6
(d), 126.7 (d), 128.0 (d), 129.0 (d), 139.5 (d), 140.0 (s), 142.0 (s), 145.4 (s), 163.0 (s). MS: 360 m/z (M+).
Anal. Calcd for C12H13IN2O3: C, 40.00; H, 3.64; N, 7.78. Found: C, 40.05; H, 3.68; N, 7.84.
Dihydropyrazole (11d) (0.90 g, 39%) as white powder having mp 100-102 °C (from ipr2O); IR (Nujol):
3400, 1720 (cm-1); 1H-NMR: 0.94 (9H, s), 3.25 (1H, dd, J = 17.8, 8.5), 3.30 (1H, dd, J = 17.8, 11.2), 3.45
(1H, dd, J = 12.0, 3.5), 3.51 (1H, dd, J = 12.0, 4.8), 3.81 (3H, s), 4.70 (1H, br s), 4.75-4.84 (1H, m), 6.87
(1H, td, J = 7.5, 1.7), 7.20-7.30 (2H, m), 7.61 (1H, dd, J = 8.5, 2.5). 13C-NMR: 21.1 (s), 28.7 (q), 34.8 (t),
52.6 (q), 63.5 (t), 68.1 (d), 125.4 (d), 127.2 (d), 129.8 (d), 137.7 (d), 139.4 (s), 140.9 (s), 146.8 (s), 162.6
(s). MS: 290 m/z (M+). Anal. Calcd for C16H22N2O3: C, 66.17; H, 7.64; N, 9.65. Found: C, 66.22; H, 7.61;
N, 9.71.
Tetrahydropyridazine (12b) (0.23 g, 10%) as white powder having mp 100-103 °C (from iPr2O); IR
(Nujol): 3400, 1730, 1710 (cm-1); 1H-NMR: 2.21-2.87 (4H, m), 3.83 (3H, s), 3.89 (3H, s), 5.37 (1H, dd, J

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963
13
= 8.4, 4.7), 5.60 (1H, br s), 7.15-8.02 (4H, m). C-NMR: 21.7 (t), 23.9 (t), 51.4 (q), 53.2 (q), 97.6 (d),
127.2 (d), 129.0 (d), 130.7 (d), 131.8 (d), 133.9 (s), 141.9 (s), 147.9 (s), 163.4 (s), 165.9 (s). MS: 292 m/z
(M+). Anal. Calcd for C14H16N2O5: C, 57.51; H, 5.52; N, 9.59. Found: C, 57.47; H, 5.49; N, 9.62.
Tetrahydropyridazine (12c) (0.86 g, 30%) as pale yellow powder having mp 140-142 °C (from iPr2O); IR
1
(Nujol): 3400, 1720 (cm-1); H-NMR: 2.17-2.76 (4H, m), 3.87 (3H, s), 4.93 (1H, dd, J = 8.0, 2.5), 5.31
13
(1H, br s), 6.90-7.90 (4H, m). C-NMR: 20.9 (t), 23.5 (t), 52.5 (q), 98.9 (d), 126.4 (d), 128.6 (d), 129.4
(d), 130.3 (d), 132.0 (s), 140.0 (s), 147.4 (s), 165.2 (s). MS: 360 m/z (M+). Anal. Calcd for C12H13IN2O3:
C, 40.00; H, 3.64; N, 7.78. Found: C, 39.95; H, 3.70; N, 7.84.
Tetrahydropyridazine (12d) (1.21 g, 52%) as white powder having mp 96-98 °C (from iPr2O); IR (Nujol):
1
3450, 1720 (cm-1); H-NMR: 0.91 (9H, s), 2.11-2.68 (4H, m), 3.85 (3H, s), 5.04 (1H, dd, J = 8.2, 3.7),
13
5.50 (1H, br s), 6.90-7.60 (4H, m). C-NMR δ 20.9 (s), 21.3 (t), 25.2 (t), 27.6 (q), 51.8 (q), 95.6 (d),
125.0 (d), 127.2 (d), 129.0 (d), 131.7 (d), 133.6 (s), 141.4 (s), 146.5 (s), 163.8 (s). MS: 290 m/z (M+).
Anal. Calcd for C16H22N2O3: C, 66.17; H, 7.64; N, 9.65. Found: C, 66.21; H, 7.60; N, 9.72.
ACKNOWLEDGEMENTS
Thanks are due to PUR for financial support. We are grateful to Dr. Lara De Benassuti, University of Milan,
for her expertise in performing NMR spectra. We are also grateful to the undergraduate student Martina Del
Bianco, University of Milan, who carried out most of the experiments described here.
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