Org. Synth. 2005, 81, 98
DOI: 10.15227/orgsyn.081.0098
SYNTHESIS OF 5-BROMOISOQUINOLINE AND 5-BROMO-8-NITROISOQUINOLINE
[Isoquinoline, 5-bromo- and Isoquinoline, 5-bromo-8-nitro-]
Submitted by William Dalby Brown
1a and Alex Haahr Gouliaev
1b.
Checked by Steven Wolff and Walter Burger.
1. Procedure
A. 5-Bromoisoquinoline. A 1-L, three-necked, round-bottomed flask equipped with an internal thermometer, mechanical stirrer, and an addition funnel fitted with a nitrogen inlet is charged with concentrated sulfuric acid (96%, 340 mL, (Note 1)) and cooled to 0°C. Isoquinoline (40 mL, 44.0 g, 330 mmol) is slowly added to the well-stirred acid at a rate such that the internal temperature is maintained below 30°C. The solution is cooled to −25°C in a dry ice-acetone bath and N-bromosuccinimide (64.6 g, 363 mmol; (Note 2)) is added to the vigorously stirred solution in portions such that the internal temperature is maintained between −22 and −26°C (Note 3). The suspension is efficiently stirred for 2 hr at −22 ± 1°C and then for 3 hr at −18 ± 1°C. The resulting homogeneous reaction mixture is poured onto 1.0 kg of crushed ice in a 5-L flask placed in an ice water bath. The reaction flask is quickly washed with ice-cold water, which is added to the 5-L flask. The resulting mixture is stirred while the pH is adjusted to 9.0 using 25% aq NH3 with the internal temperature maintained below 25°C. The resulting alkaline suspension is added to 800 mL of diethyl ether and the biphasic system is vigorously mixed (Note 4). The two clear phases are separated and the aqueous phase is extracted with two 200-mL portions of diethyl ether. The combined organic phases are washed with 200 mL of 1M NaOH (aq) and 200 mL of H2O, dried over anhydrous MgSO4, filtered, and concentrated to afford 47 g of a light brown solid. Fractional distillation under reduced pressure (bp 145-149°C at 14 mm, (Note 5)) furnishes 34-36 g (47-49%) of 5-bromoisoquinoline as a white solid (Notes 6 and 7).
B. 5-Bromo-8-nitroisoquinoline. A 1-L, three-necked, round-bottomed flask fitted with an internal thermometer, mechanical stirrer, and an addition funnel fitted with a nitrogen inlet is charged with concentrated sulfuric acid (96%, 340 mL, (Note 1)) and cooled to 0°C. Isoquinoline (40 mL, 44.0 g, 330 mmol) is slowly added from the addition funnel to the well-stirred acid such that the internal temperature is maintained below 30°C. The solution is cooled to −25°C in a dry ice-acetone bath and N-bromosuccinimide (76.4 g, 429 mmol; (Note 2)) is added to the vigorously stirred solution in portions such that the internal temperature is maintained between −22 and −26°C (Note 3). The suspension is efficiently stirred for 2 hr at −22°C ± 1°C and then for 3 hr at −18°C ± 1°C. Potassium nitrate (35.0 g, 346 mmol) is then added at a rate such as to maintain the internal temperature below −10°C and the mixture is then stirred at −10°C for 1 hr. The cooling bath is removed and the solution is stirred overnight. The resulting homogeneous reaction mixture is poured onto 1.0 kg of crushed ice in a 5-L flask and the reaction flask is quickly washed with ice-cold water, which is added to the 5-L flask. The resulting mixture is stirred while the pH is adjusted to 8.0 using 25% aq NH3 with the internal temperature maintained below 30°C. The resulting suspension is stirred in an ice water bath for 2 hr and the precipitated solids are isolated by filtration using a glass filter funnel. The solids are thoroughly washed three times with 1-L portions of ice-cold water and then air-dried to constant weight to afford 65 g of a slightly yellow solid. This material is suspended in 1000 mL of heptane and 250 mL of toluene (Note 8) in a 2-L, round-bottomed flask and heated at reflux for 1.5 hr with stirring. The hot solution is then filtered through Celite using vacuum suction (Note 9). The volume of the filtrate is reduced by distillation to 1000 mL and the resulting orange solution is allowed to slowly cool with stirring overnight. The solids are isolated by filtration, washed with 350 mL of ice-cold heptane, and air-dried to constant weight to afford 40-44 g (47-51%) of 5-bromo-8-nitroisoquinoline (Notes 10 and 11).
2. Notes
1.
Sulfuric acid 96% (technical quality) and diethyl ether (technical quality) were purchased from Bie & Berntsen A/S, Sandbaekvej 7, DK-2610 Roedovre, Denmark and used without further purification.
Isoquinoline (97%) and potassium nitrate (99%) were purchased from Aldrich Chemical Company, Inc. and used without further purification.
2.
Isoquinoline must be completely dissolved prior to the addition of
N-bromosuccinimide.
N-Bromosuccinimide (99%) was purchased from Aldrich Chemical Company, Inc. and recrystallized
2 and air-dried prior to use. Recrystallization is essential in order to obtain high yield and pure product. The use of more NBS than stated (i.e., more than 1.1 equiv for the synthesis of
5-bromoisoquinoline and 1.3 equiv for the synthesis of
5-bromo-8-nitroisoquinoline) to obtain complete transformation of
isoquinoline should be avoided as this leads to formation of
5,8-dibromoisoquinoline, which cannot easily be separated from
5-bromoisoquinoline and which will also lead to a lower yield of
5-bromo-8-nitroisoquinoline.
3.
The temperature is controlled throughout the reaction by intermittently adding additional pieces of dry ice to the
dry ice-acetone bath. Strict temperature control throughout the bromination reaction is important to obtain high regioselectivity and purity of the product as the side products cannot be removed with ease.
4.
Vigorous shaking for at least 5 min is required.
5.
A 40-cm column insulated with cotton and aluminum foil is used for the fractional distillation. The
condenser is heated to a constant temperature of 80°C by attaching a 80°C
water bath and a
circulatory pump. As distillation progresses, the temperature rises smoothly, settling at 126-128°C for some time, and then rising to 144°C (at 14 mm), at which temperature and pressure the product starts to solidify in the condenser. Increased heating (heating the water bath to 85-90°C) allows for a steady flow of product through the condenser. All fractions boiling below 144°C/14 mm are discarded. As an alternative to the preheated condenser, a heat gun may be used to melt the solidifying product.
6.
The isolated product typically contains 0-3%
isoquinoline. Physical data for
5-bromoisoquinoline: TLC: R
f = 0.30 (
9:1 dichloromethane/diethyl ether); IR (CHCl
3) cm
−1: 3053, 1582, 1509, 1484, 1352, 1263, 1222, 1112, 1000;
1H NMR
pdf (500 MHz, DMSO-d
6) δ: 7.62 (t, 1 H, J = 7.8), 7.91 (d, 1 H, J = 6.0), 8.15 (d, 1 H, J = 7.5), 8.19 (d, 1 H, J = 8.2), 8.66 (d, 1 H, J = 5.9), 9.37 (s, 1 H);
13C NMR (DMSO-d
6) δ: 118.5, 120.3, 127.9, 128.4, 129.3, 133.9, 134.3, 144.6, 152.9.
7.
Alternatively, the product can be isolated in >99% purity by column chromatography on 63-200 µm silica gel eluting with 9:1 → 5:1
dichloromethane/ethyl acetate and then 9:1 → 4:1
dichloromethane/diethyl ether. The product obtained in this manner has
mp 81-82°C (lit. 82-84°C,3 79.5-80.5°C,4 82-83°C5). Anal. Calcd for C
9H
6BrN: C, 51.96; H, 2.91; Br, 38.40; N, 6.73. Found: C, 52.06; H, 2.74; Br, 38.21; N, 6.65.
8.
Heptane was purchased from Fisher Chemicals and
toluene (technical quality) was purchased from SvedaKemi A/S, Rosenoerns Allé 9, DK-1970 Frederiksberg, Denmark.
9.
The
glass filter funnel containing Celite was preheated using a heat gun to avoid precipitation of product in the funnel. After filtration, an additional preheated mixture of
120 mL of heptane and 30 mL of toluene was passed through the Celite using suction. A precipitate forms in the filtrate, which is redissolved by heating to reflux.
10.
The isolated product typically contains 0-1%
8-bromo-5-nitroisoquinoline, 0-1%
5,8-dibromoisoquinoline, and 0-1%
5-nitroisoquinoline. Physical data for
5-bromo-8-nitroisoquinoline:
mp 137-139°C (lit. 139-141°C,3 138-140°C,4 139-141°C5); TLC R
f = 0.57 (9:1
dichloromethane/ethyl acetate); IR (CHCl
3) cm
−1: 3053, 1619, 1580, 1485, 1374, 1265, 1201;
1H NMR
pdf (500 MHz, DMSO-d
6) δ: 8.12 (dd, 1 H, J
A = 0.8, J
B = 6.0), 8.33
† (d, 1 H, J = 8.3), 8.35 (AB, 1 H, J = 8.2), 8.84 (d, 1 H, J = 5.9), 9.78 (s, 1 H);
13C NMR δ: 118.9, 120.0, 125.8, 127.8, 133.4, 134.5, 145.3, 145.7, 148.1.
11.
Alternatively, the product can be isolated in >99% purity by column chromatography on 63-200 µm silica gel, elution with 9:1 → 6:1
dichloromethane/diethyl ether followed by recrystallization to yield
5-bromo-8-nitroisoquinoline with
mp 139-141°C. Anal. Calcd for C
9H
6BrN: C, 42.72; H, 1.99; Br, 31.58; N, 11.07. Found: C, 43.03; H, 1.82; Br, 31.19; N, 10.94.
Handling and Disposal of Hazardous Chemicals
The procedures in this article are intended for use only by persons with prior training in experimental organic chemistry. All hazardous materials should be handled using the standard procedures for work with chemicals described in references such as "Prudent Practices in the Laboratory" (The National Academies Press, Washington, D.C., 2011 www.nap.edu). All chemical waste should be disposed of in accordance with local regulations. For general guidelines for the management of chemical waste, see Chapter 8 of Prudent Practices.
These procedures must be conducted at one's own risk. Organic Syntheses, Inc., its Editors, and its Board of Directors do not warrant or guarantee the safety of individuals using these procedures and hereby disclaim any liability for any injuries or damages claimed to have resulted from or related in any way to the procedures herein.
3. Discussion
Previously published methods for electrophilic bromination of isoquinoline
3-5 lead to mixtures of isomers only separable with difficulty, use expensive additives or large excesses of reactants, or involve multistep procedures.
The present procedure describes conditions, which allow for the formation of 5-bromoisoquinoline in good yield and high purity using easily available and inexpensive starting materials. In order to obtain the desired product, it is important to ensure careful temperature control to suppress the formation of 8-bromoisoquinoline, which is difficult to remove. By choosing sulfuric acid as solvent for the bromination, a convenient one-pot procedure to prepare 5-bromo-8-nitroisoquinoline, without prior isolation of 5-bromoisoquinoline, has been developed. Finally, the method can easily be scaled up from grams to kilograms of the title compounds.
Many pharmacologically active compounds have been synthesized using
5-bromoisoquinoline or
5-bromo-8-nitroisoquinoline as building blocks.
6,7,8,9,10,11 The haloaromatics participate in transition-metal couplings
8,10,12 and Grignard reactions. The readily reduced nitro group of
5-bromo-8-nitroisoquinoline provides access to an aromatic amine, one of the most versatile functional groups. In addition to
N-alkylation,
N-acylation and diazotiation, the amine may be utilized to direct electrophiles into the
ortho-position.
The heterocyclic ring may be reduced under very mild conditions after
N-alkylation, giving access to bicyclic amines,
7-10,13 or enamines
5 Use of
5-bromoisoquinoline in a metalation reaction yielded
6-aminoisoquinoline, a compound otherwise accessed with difficulty.
14
Appendix
Chemical Abstracts Nomenclature (Collective Index Number);
(Registry Number)
Isoquinoline; (119-65-3)
N-Bromosuccinimide:
2,5-Pyrrolidinedione, 1-bromo-; (128-08-5)
5-Bromoisoquinoline:
Isoquinoline, 5-bromo-; (34784-04-8)
5-Bromo-8-nitroisoquinoline:
Isoquinoline, 5-bromo-8-nitro-; (63927-23-1)
Potassium nitrate; (7757-79-1)
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