Supplementary data

Supplementary data

Montmorillonite KSF catalyzed synthesis of 4-heteroarylidene-

N-arylhomophthalimides by Knoevenagel condensation

Varadhan Krishnakumara,b, Fazlur- Rahman Nawaz Khana,c*, Badal Kumar Mandalb*, Euh-Duck Jeongc*, Jong Sung Jin c*

aOrganic and Medicinal Chemistry Research Laboratory, Organic Chemistry Division,

School of Advanced Sciences, VIT-University, Vellore 632 014, Tamil Nadu, India.

bTrace Elements Speciation Research Laboratory,

Environmental and Analytical Chemistry Division,School of Advanced Sciences,

VIT-University, Vellore 632 014, Tamil Nadu, India.

cKorea Basic Science Institute, Busan Center, Busan 618 230, South Korea

*Correspondence: E-mail; Prof. F. Nawaz Khan: nawaz_f@yahoo.co.in

Prof. B. K. Mandal: mbadal@hotmail.com; Dr ED Jeong, edjeong@kbsi.re.kr

Dr JS Jin jsjin@kbsi.re.kr

(E) 4-((2-Chloroquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione (3a) Yellow solid, mp 152-154 oC, IR (KBr) 1710 (C3-CO), 1674 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.31-8.33 (d, J = 7.2 Hz, 2H), 8.22 (s, 1H), 8.08-8.11 (d, J = 8.4 Hz, 1H), 7.80-7.84 (t, J = 7.6 Hz, 1H), 7.72-7.74 (d, J = 8.0 Hz, 1H), 7.53-7.57 (m, 2H), 7.45-7.50 (m, 2H), 7.38-7.40 (d, J = 8.0 Hz, 1H), 7.26-7.31 (m, 4H), ppm. 13C NMR (100MHz, CDCl3) 165.10 (C3-CO), 164.04 (C1-CO), 149.17, 147.76, 138.78, 137.96, 135.21, 133.15, 131.66, 131.50, 129.96, 129.69, 129.42, 128.88, 128.61, 128.48, 128.34, 127.85, 127.82, 126.74, 126.65, 126.17, 30.96, ppm. LCMS m/z calcd for C25H15ClN2O2 m/e 410.08, found 410.00.

(E) 4-((2-Chloro-8-methylquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione (3b) Yellow solid, mp 231-233 oC, IR (KBr) 1707 (C3-CO), 1660 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.48 (s, 1H), 8.33-8.36 (d, J = 6.8 Hz, 1H), 8.08 (s, 1H), 7.98-8.00 (d, J = 8.0 Hz, 1H), 7.77-7.81 (t, J = 6.0 Hz, 1H), 7.60-7.65 (m, 2H), 7.55-7.56 (d, J = 6.8 Hz, 1H), 7.38-7.48 (m, 4H), 7.19-7.21 (m, 2H), 2.74 (s, 3H), ppm. 13C NMR (100MHz, CDCl3) 164.10 (C3-CO), 163.57 (C1-CO), 149.50, 147.77, 147.77, 144.32, 139.53, 137.59, 134.70, 134.64, 134.46, 134.46, 134.38, 133.17, 129.86, 129.40, 129.22, 129.06, 128.37, 128.29, 128.16, 127.87, 125.84, 123.32, 21.06, ppm. LCMS m/e calcd for C26H17ClN2O2 m/e 424.09

(E) 4-((2-Chloro-6-methylquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione (3c) Pale yellow solid, mp 240-242 oC, IR (KBr) 1715 (C3-CO), 1673 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.31-8.32 (d, J = 5.2 Hz, 2H), 8.11 (s, 1H), 7.97-7.99 (d, J = 8.4 Hz, 1H), 7.62-7.65 (d, J = 6.8 Hz, 1H), 7.46-7.57 (m, 4H), 7.44 (s, 1H), 7.38-7.40 (d, J = 8.8 Hz, 1H), 7.28-7.31 (m, 3H), 2.74 (s, 3H), ppm. 13C NMR (100MHz, CDCl3) 164.93 (C3-CO), 163.87 (C1-CO), 148.11, 146.43, 139.36, 138.04, 137.23, 134.79, 133.99, 133.64, 133.26, 131.54, 129.94, 129.66, 129.61, 128.63, 128.29, 127.96, 126.81, 126.67, 126.60, 125.95, 21.59, ppm. LCMS m/e calcd for C26H17ClN2O2 m/e 424.09, found 425.00.

(E) 4-((2-Chloro-6-methoxyquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione (3d) Yellow solid, mp 234-236 oC, IR (KBr) 1714 (C3-CO), 1672 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.30-8.33 (d, J = 7.2 Hz, 2H), 8.08 (s, 1H), 7.97-7.99 (d J = 9.2 Hz, 1H), 7.53-7.57 (m, 2H), 7.43-7.50 (m, 3H), 7.37-7.40 (d, J = 7.2 Hz, 1H), 7.28-7.33 (m, 3H), 6.96 (d, J = 2.8 Hz, 1H), 3.90 (s, 3H), ppm. 13C NMR (100MHz, CDCl3) 165.08 (C3-CO), 164.03 (C1-CO), 158.69, 146.38, 143.88, 139.14, 136.49, 135.25, 133.13, 131.61, 129.99, 129.90, 129.59, 129.38, 129.09, 128.84, 128.49, 128.23, 127.85, 126.79, 126.17, 124.36, 105.18, 55.71, ppm. LCMS m/e calcd for C26H17ClN2O3 m/e 440.09, found 441.00.

(E) 4-((2-Chloro-7,8-dimethylquinolin-3-yl)methylene)-2-phenylisoquinoline 1,3(2H,4H)-dione (3e) Pale orange solid, mp 194-196 oC, IR (KBr) 1708 (C3-CO), 1668 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.29-8.32 (d, J = 4.8 Hz, 2H), 8.12 (s, 1H), 7.52-7.56 (t, J = 7.2 Hz, 2H), 7.44-7.49 (m, 3H), 7.38-7.42 (t, J = 7.6 Hz, 1H), 7.25-7.30 (m, 4H), 2.75 (s, 3H), 2.53 (s, 3H), ppm. 13C NMR (100MHz, CDCl3) 165.16 (C3-CO), 164.07 (C1-CO), 147.97, 146.99, 140.01, 139.47, 138.05, 134.30, 133.01, 131.76, 130.56, 129.83, 129.46, 129.35, 128.78, 128.51, 127.82, 127.29, 126.71, 126.15, 125.04, 124.72, 20.87, 13.34, ppm. LCMS m/e calcd for C27H19ClN2O2 m/e 438.11.

(E) 4-((2-Chlorobenzo[h]quinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione (3f) Yellow solid, mp >300 oc(charring), IR (KBr) 1710 (C3-CO), 1657 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 9.16-9.18 (d, J = 2.4 Hz, 1H), 8.57 (s, 1H), 8.34-8.36 (d, J = 6.4 Hz, 1H), 8.12 (s, 1H), 8.00-8.02 (d, J = 8.0 Hz, 1H), 7.87-7.89 (m, 1H), 7.77-7.86 (m, 2H), 7.69-7.72 (m, 2H), 7.60-7.66 (m, 2H), 7.44-7.48 (m, 2H), 7.36-7.40 (m, 1H), 7.20-7.22 (d, J = 5.2 Hz, 2H), ppm. LCMS m/e calcd for C29H17ClN2O2 m/e 460.09, found 461.00.

(E) 2-(4-Chlorophenyl)-4-((2chloroquinolin-3-yl)methylene)isoquinoline-1,3(2H,4H)-dione (3g) Yellow solid, mp 258-260 oC, IR (KBr) 1710 (C3-CO), 1666 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.30-8.32 (t, J = 3.2 Hz, 2H), 8.21 (s, 1H), 8.09-8.11 (d, J = 8.4 Hz, 1H), 7.82-7.84 (t, J = 5.6 Hz, 1H), 7.72-7.74 (d, J = 8.0 Hz, 1H), 7.60-7.62 (t, J = 6.0 Hz, 1H), 7.50-7.53 (m, 2H), 7.45-7.47 (m, 1H), 7.38-7.40 (d, J = 7.6 Hz, 1H), 7.30-7.32 (d, J = 4.4 Hz, 1H), 7.23-7.25 (m, 2H), ppm. 13C NMR (100MHz, CDCl3) 164.92 (C3-CO), 163.85 (C1-CO), 149.07, 147.79, 139.05, 134.81, 133.61, 133.28, 131.69, 131.46, 129.97, 129.93, 129.74, 129.62, 128.78, 128.14, 127.83, 126.76, 126.60, 125.96, ppm. LCMS m/e calcd for C25H14Cl2N2O2 m/e 444.04, found 446.60.

(E) 4-((2-Chloro-8-methylquinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione (3h) Yellow solid, mp 240-242 oC, IR (KBr) 1718 (C3-CO), 1676 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.29-8.32 (t, J = 6.8 Hz, 2H), 8.15 (s, 1H), 7.64-7.66 (d, J = 6.8 Hz, 1H), 7.38-7.56 (m, 7H), 7.29-7.31 (d, J = 6.0 Hz, 1H), 7.22-7.25 (m, 2H), 2.81 (s, 3H), ppm. 13C NMR (100MHz, CDCl3) 164.96 (C3-CO), 163.88 (C1-CO), 149.94, 147.03, 139.45, 138.14, 136.96, 134.76, 133.68, 133.25, 131.74, 131.58, 129.95, 129.64, 129.60, 128.39, 127.90, 127.54, 126.77, 126.66, 125.92, 125.70, 17.73, ppm. LCMS m/e calcd for C26H16Cl2N2O2 m/e 458.05.

(Z) 4-((2-Chloro-6-methylquinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione (3i) Yellow solid, mp 270-272 oC, IR (KBr) 1710 (C3-CO), 1668 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.30-8.31 (t, J = 4.0 Hz, 2H), 8.10 (s, 1H), 7.97-7.99 (d, J = 8.4 Hz, 1H), 7.63-7.65 (d, J = 6.8 Hz, 1H), 7.50-7.52 (d, J = 6.8 Hz, 2H), 7.44-7.47 (m, 2H), 7.38-7.40 (d, J = 7.6 Hz, 1H), 7.27-7.30 (m, 1H), 7.23-7.25 (m, 2H), 2.53 (s, 3H), ppm. LCMS m/e calcd for C26H16Cl2N2O2 m/e 458.05, found 460.80.

(E) 4-((2-Chloro-7-methylquinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione (3j) Yellowish orange solid, mp >300 oC, IR (KBr) 1699 (C3-CO), 1657 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.53 (s, 1H), 8.32-8.35 (d, J = 6.4 Hz, 1H), 8.08 (s, 1H), 7.97-7.99 (d, J = 8.0 Hz, 1H), 7.77-7.81 (t, J = 8.4 Hz, 2H), 7.70-7.72 (d, J = 8.0 Hz, 1H), 7.60-7.64 (t, J = 7.6 Hz, 1H), 7.41-7.43 (d, J = 4.8 Hz, 2H), 7.36-7.38 (d, J = 8.0 Hz, 1H), 7.14-7.16 (d, J = 4.8 Hz, 2H), 2.55 (s, 3H), ppm. LCMS m/e calcd for C26H16Cl2N2O2 m/e 458.05, found 459.80.

(E) 4-((2-Chloro-6-methoxyquinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione (3k) Yellow solid, mp 242-244 oC, IR (KBr) 1715 (C3-CO), 1671 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.29-8.32 (d, J = 4.0 Hz, 2H), 8.07 (s, 1H), 7.96-7.99 (d J = 9.2 Hz, 1H), 7.50-7.52 (m, 2H), 7.43-7.46 (m, 2H), 7.37-7.39 (d, J = 7.2 Hz, 1H), 7.29-7.33 (t, J = 5.6 Hz, 1H), 7.23-7.25 (m, 2H), 6.95-6.96 (d, J = 2.8 Hz, 1H), 3.90 (s, 3H), ppm. 13C NMR (100MHz, CDCl3) 164.93 (C3-CO), 163.87 (C1-CO), 158.73, 146.28, 143.91, 139.44, 136.46, 134.81, 133.66, 133.29, 131.58, 130.01, 129.95, 129.67, 129.62, 128.95, 128.05, 127.82, 126.83, 125.95, 124.41, 105.19,55.71, ppm. LCMS m/e calcd for C26H16Cl2N2O3 m/e 474.05.

(E) 4-((2-Chloro-7,8-dimethylquinolin-3-yl)methylene)-2-(4-chlorophenyl) isoquinoline-1,3(2H,4H)-dione (3l) Greenish yellow solid, mp 198-200 oC, IR (KBr) 1712 (C3-CO), 1674 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 8.29-8.33 (d, J = 8.4 Hz, 2H), 8.11 (s, 1H), 7.49-7.52 (d, J = 8.8 Hz, 2H), 7.39-7.47 (m, 4H), 7.29 (d, J = 1.2 Hz, 1H), 7.22-7.27 (m, 2H), 2.75 (s, 3H), 2.54 (s, 3H), ppm. 13C NMR (100MHz, CDCl3) 165.01 (C3-CO), 163.91 (C1-CO), 147.87, 147.01, 140.09, 139.78, 138.03, 134.74, 134.32, 133.71, 133.17, 131.71, 130.59, 129.95, 129.85, 129.58, 129.52, 127.60, 127.15, 126.74, 125.91, 125.00, 124.71, 20.86, 13.33, ppm. LCMS m/e calcd for C27H18Cl2N2O2 m/e 472.07.

(E) 4-((2-Chlorobenzo[h]quinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione (3m) Yellow solid, mp >300 oC (charring), IR (KBr) 1712 (C3-CO), 1676 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 9.16-9.19 (d, J = 2.8 Hz, 1H), 8.55 (s, 1H), 8.34-8.36 (d, J = 6.4 Hz, 1H), 8.14 (s, 1H), 8.01-8.03 (d, J = 8.0 Hz, 1H), 7.87-7.90 (m, 1H), 7.79-7.83 (m, 2H), 7.70-7.73 (m, 2H), 7.61-7.67 (m, 2H), 7.41-7.43 (d, J = 4.4 Hz, 2H), 7.14-7.16 (d, J = 4.4 Hz, 2H), ppm. 13C NMR (100MHz, CDCl3) 164.02 (C3-CO), 163.06 (C1-CO), 149.19, 147.82, 142.27, 140.16, 139.90, 139.09, 138.97, 134.76, 134.43, 134.40, 133.46, 130.00, 129.67, 129.61, 129.55, 128.07, 127.42, 127.07, 126.66, 124.93, 124.90, 124.66, 124.35, 123.33, ppm. LCMS m/e calcd for C29H16Cl2N2O2 m/e 494.05, found 494.80.

(E) 4-(2-Chlorobenzylidene)-2phenylisoquinoline-1,3(2H,4H)-dione (3n) Greenish yellow solid, mp 190-192 oC, IR (KBr) 1721 (C3-CO), 1674 (C1-CO) cm-1 1H NMR (400MHz, CDCl3) 7.51-7.55 (m, 3H), 7.42-7.48 (m, 2H), 7.30-7.39 (m, 4H), 7.27-7.29 (m, 3H), 7.23-7.23 (d, J = 0.8 Hz, 2H), ppm. 13C NMR (100MHz, CDCl3) 165.30 (C3-CO), 164.17 (C1-CO), 141.54, 135.41, 134.79, 134.79, 133.75, 132.87, 132.00, 130.57, 130.33, 129.57, 129.37, 129.31, 129.22, 128.71, 128.52, 127.17, 126.98, 125.92, ppm. LCMS m/e calcd for C22H14ClNO2 m/e 359.07.

1H NMR spectra of (E) 4-((2-chloroquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione

13C NMR spectra of 4-((2-chloroquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione 1H NMR spectra of (E) 4-((2-chloro-8-methylquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione

13C NMR spectra of (E) 4-((2-chloro-8-methylquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione

1H NMR spectra of (E) 4-((2-chloro-6-methylquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione

13C NMR spectra of (E) 4-((2-chloro-6-methylquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione

1H NMR spectra of (E) 4-((2-chloro-6-methoxyquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione

13C NMR spectra of (E) 4-((2-chloro-6-methoxyquinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione

1H NMR spectra of (E) 4-((2-chloro-7,8-dimethylquinolin-3-yl)methylene)-2-phenylisoquinoline 1,3(2H,4H)-dione 13C NMR spectra of (E) 4-((2-chloro-7,8-dimethylquinolin-3-yl)methylene)-2-phenylisoquinoline 1,3(2H,4H)-dione

1H NMR spectra of (E) 4-((2-chlorobenzo[h]quinolin-3-yl)methylene)-2-phenylisoquinoline-1,3(2H,4H)-dione

1H NMR spectra of (E) 2-(4-chlorophenyl)-4-((2chloroquinolin-3-yl)methylene)isoquinoline-1,3(2H,4H)-dione

13C NMR spectra of (E) 2-(4-chlorophenyl)-4-((2chloroquinolin-3-yl)methylene)isoquinoline-1,3(2H,4H)-dione

1H NMR spectra of (E) 4-((2-chloro-8-methylquinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione

13C NMR spectra of (E) 4-((2-chloro-8-methylquinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione

1H NMR spectra of (E) 4-((2-chloro-7-methylquinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione

1H NMR spectra of (E) 4-((2-chloro-6-methylquinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione

1H NMR spectra of (E) 4-((2-chloro-6-methoxyquinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione

13C NMR spectra of (E) 4-((2-chloro-6-methoxyquinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione

1H NMR spectra of (E) 4-((2-chloro-7,8-dimethylquinolin-3-yl)methylene)-2-(4-chlorophenyl) isoquinoline-1,3(2H,4H)-dione

13C NMR spectra of (E) 4-((2-chloro-7,8-dimethylquinolin-3-yl)methylene)-2-(4-chlorophenyl) isoquinoline-1,3(2H,4H)-dione

1H NMR spectra of (E) 4-((2-chlorobenzo[h]quinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione

13C NMR spectra of (E) 4-((2-chlorobenzo[h]quinolin-3-yl)methylene)-2-(4-chlorophenyl)-isoquinoline-1,3(2H,4H)-dione

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