WO2020202180A1

WO2020202180A1 - Indole-ynone mediated benzoannulation process for the preparation of carbazoles- carbazomycin a, calothrixin b and staurosporinone

Info

Publication number: WO2020202180A1
Application number: PCT/IN2020/050275
Authority: WO
Inventors: Srihari Pabbaraja; Goverdhan Mehta; Ramesh Samineni; Shweta SINGH
Original assignee: Council Of Scientific & Industrial Research
Priority date: 2019-03-29
Filing date: 2020-03-24
Publication date: 2020-10-08
Also published as: US20220169609A1; EP3947333A1; EP3947333A4

Abstract

The present invention relates to carbazoles of general formula (I), and process for the preparation thereof: wherein 'R₁' is H, C1-C6 alkyl, benzyl, or allyl; R₂ is H, C1-C6 alkyl, cyclopropyl, phenyl, aryl, heteroaryl, or NO₂; R₃ is H, C1-C6 alkyl, cyclopropyl, phenyl aryl, heteroaryl, 4-methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, or 2-Fluoro phenyl; R₄ is H, benzoyl, -CO₂Et, -CHO, Br, or -OMe; R₅ is OH, OMOM, OMe, CN, or OTf; R₆ is H, or O-alkyl; and R₃-R₄ is -CHNCH2CH2-. This invention also relates to the process for the preparation of carbazomycin A of Formula (1), calothrixin B of Formula (2) and staurosporinone of Formula (3) involving carbazoles of general formula (I) as an intermediate.

Description

INDOLE- YNONE MEDIATED BENZOANNULATION PROCESS FOR THE PREPARATION OF CARBAZOLES- CARBAZOMYCIN A, CALOTHRIXIN B AND STAUROSPORINONE FIELD OF THE INVENTION

The present invention relates to carbazoles of general formula (I), and process for the preparation thereof:

Formula I

wherein‘Ri’ is H, C1-C6 alkyl, benzyl, or allyl; R2 is H, C1-C6 alkyl, cyclopropyl, phenyl, aryl, heteroaryl, or NO2; R3 is H, C1-C6 alkyl, cyclopropyl, phenyl aryl, heteroaryl, 4- methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, or 2-Fluoro phenyl; R4 is H, benzoyl, - CC Et, -CHO, Br, or -OMe; R5 is OH, OMOM, OMe, CN, or OTf; R₆ is H, or O-alkyl; and R3-R4 is -CHNCH2CH2-. This invention also relates to the process for the preparation of carbazomycin A of Formula (1), calothrixin B of Formula (2) and staurosporinone of Formula (3) involving carbazoles of general formula (I) as an intermediate.

carbazomycin A (1 ) calothrixin B (2) staurosporinone (3)

In particular, the invention also relates to the total synthesis of carbazomycin A of Formula (1), calothrixin B of Formula (2) and staurosporinone of Formula (3).

BACK GROUND OF THE INVENTION

The present protocol focusses on the synthesis of the tricyclic nitrogen containing heterocyclic compounds called carbazoles, which are frequently encountered in natural products that are known to display therapeutic properties such as anti-cancer, anti inflammatory, anti-viral, anti-oxidative, anti-mitotic, antipsychotic, and antibiotic properties (The Alkaloids: Chemistry and biology, 2008, 65, 181-193; Bioorg. Med. Chem. Lett., 2010, 20, 1881; Molecules, 2015, 20, 13496-13517; Tetrahedron 2011, 67, 7593-7597, US20150342927). Few carbazoles are also used in the treatment of ischemic heart diseases and congestive heart failures (J. Med. Chem. 2013, 21,8626). Furthermore, this class of compounds also serve as useful building blocks in organic materials due to their hole transporting, light-emitting, photoconductive and photorefractive properties (Org. Lett. 2014, 16, 2292; Chem. Commun. 2013, 49, 2822, Chem. Rev., 2012, 112, 2208; J. Am. Chem. Soc., 2001, 123, 9404; Adv. Mater., 2014, 26, 7543, US9, 911,925, US4297426). Because of the potential applications of these carbazole motif containing molecules, they have attracted significant attention from synthetic chemists towards developing new methods for their preparation ((Chem. Rev., 2002, 102, 4303; Tetrahedron 2012, 68, 6099-6121; Isr. J. Chem. 2018, 58, 608-621). While there are methods involved using transition-metal mediated cyclization’s and construction of tricyclic moieties starting from indoles, the classical methods for accessing carbazoles include Fischer-Borsche synthesis and Cadogan cyclization (J. Chem. Soc., Perkin Trans. 1, 1990, 2475 J. Chem. Soc., 1965, 4831, Synthesis, 1969, 11). Various synthetic schemes are provided for the carbazoles. They can be synthesized from 2- amino diphenyl by heating at elevated temperatures (US patent 2,328,588, US2921942A, others include treatment of cyclohexane- 1,3-dione with phenyl hydrazine and conversion to carbazole (US20070197797A1).

Recently, nitromethane has been used as a one carbon linker with aryl-ynones resulting in the formation of two new C-C bonds with variation in the reactivity pattern to form naphthalene skeletons (Angewandte Chemie Int. Ed. Eng. 2018, 57, 16847). The present process demonstrates the benzoannulation of indole-ynones with nitromethane to synthesize several carbazole molecules of formula I, II, and III. The products (carbazoles) obtained by this process have been utilized further to achieve the total synthesis of natural products carbazomycin A (Chem. Pharm. Bull. 2018, 66, 178-183; Org. Lett. 2014, 16, 5470-5473), calothrixin B (Mar. Drugs 2016, 14, 17; Org. Chem. Front., 2018, 5, 590-594) and staurosporinone (Chem. Sci., 2016, 7, 2706-2710) in good yields.

The antibiotic carbazomycin A is structurally diverse 3,4-dioxygenated carbazole alkaloid which is isolated from streptomyces ehimense H 1051-MY by Nakamura et al in 1980 (J. Antibiotics, 1980, 33, 683). The carbazomycins A and B displayed inhibitory activity against 5-lipoxygenase, and have weak antibacterial and anti yeast activities. Because of these activities, they have attracted significant attention by the chemists towards their synthesis. The first synthetic route for carbazomycin A involves the Diels Alder approach followed by functional groups interconversions (J. Chem. Soc. Perkin Transactions I, 1989, 0, 376) and was followed by several other synthetic approaches (for latest approach see Org. Lett. 2014, 16, 5470). The construction of fully substituted benzene ring has been the key factor. Despite several efforts have been focused to develop regio selective installation of appropriate substituents, the general and efficient methods are still limited (Chem. Rev. 2012, 112, 3193, Chem Rev. 2002, 102, 4303; Org. Lett. 2014, 16, 5156). The unique pentacyclic alkaloid, calothrixin B was isolated from calothrix cyanobacteria (Tetrahedron 1999, 55, 13513) and was found to display antimalarial and antiproliferative properties against HeLa cancer cells (Bioorg. Med. Chem. Lett. 2012, 22, 4762; J. Med. Chem. 2004, 47, 4958; J. Nat. Prod. 2009, 72, 438). The interesting biological properties of calothrixins have attracted significant attention from chemists towards their synthesis (Org. Lett. 2000, 2, 3735; Heterocycles 2009, 77, 85; Tetrahedron Lett. 2012, 53, 2894). The key known steps for its synthesis include ortho-lithiation strategy, palladium catalyzed intramolecular cross coupling reactions etc (J. Org. Chem. 2013, 78, 2802). and several other syntheses are known involving two biosynthetic routes (Tetrahedron 2007, 63, 10963; Tetrahedron Lett. 2006, 47, 5859).

The bioactive indolocarbazole alkaloid k-252c named as staurosporinone was isolated in 1986 from culture broths of Nocardiopsis sp K-252 and Nocardiopsis Sp. K-290 (J. Antibiot., 1986, 34, 1059, J. Antibiot., 1986, 34, 1066, J. Antibiot., 1986, 34, 1072). This compound is known to be potent inhibitor of protein kinase C which lays a crucial role in signal transduction pathways associated with metabolism, gene expression and cell proliferation (J. Biol. Chem., 1982, 257, 7847; Nature, 1984, 308, 693). The aglycone of staurosporine has attracted significant attention from chemists because of the interesting biological activity and novel functional pattern of the hexasubstituted arene framework. Some of the key synthetic methods involve metal catalyzed C-H amination and C-H carbonylation reactions along with several other key reactions (Org. Lett., 2001, 3, 1689; J. Am. Chem. Soc., 1997, 119, 9652, for staurosporine derivatives see US5093330A).

OBJECTIVE OF THE INVENTION

The main object of the present invention is to provide a present invention relates to carbazoles of general formula (I), and process for the preparation thereof:

Formula I

wherein‘Ri’ is H, C1-C6 alkyl, benzyl, or allyl; R2 is H, C1-C6 alkyl, cyclopropyl, phenyl, aryl, heteroaryl, C1-C6 methoxy carbonyl, or NO2; R3 is H, C1-C6 alkyl, cyclopropyl, phenyl aryl, heteroaryl, 4-methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, 2-Fluoro phenyl, 4- Fluoro phenyl, or 4-butyl phenyl; R4 is H, benzoyl, -CC Et, -CHO, Br, or -OMe; R5 is OH, OMOM, OMe, CN, or OTf; R₆ is H, or O-alkyl; and R3-R4 is -CHNCH2CH2-.

Another objective of the present invention is to provide the process for the preparation of carbazomycin A of Formula (1), calothrixin B of Formula (2) and staurosporinone of Formula (3) involving carbazoles of general formula (I) as an intermediate.

carbazomycin A (1 ) calothrixin B (2) staurosporinone (3)

In another objective of the invention is to provide the total synthesis of carbazomycin A of Formula (1), calothrixin B of Formula (2) and staurosporinone of Formula (3).

In yet another objective of the present invention is to provide a new and efficient processes and intermediates for the preparation of carbazoles through benzoannulation of indolo-ynones with nitromethane and its derivatives.

Another objective of the present invention is to provide the process, which could be carried out by employing two C-C bond activation protocol using a strategy of benzoannulation of indole-ynone and nitromethane.

Another objective of the present invention is to extend the strategy and utilize one of the obtained carbazole product for the total synthesis of natural product carbazomycin A in a concise approach.

Another objective of the present invention is to extend the strategy and utilize one of the obtained nitro-substituted carbazole product for the total synthesis of natural product calothrixin B in a concise approach.

Another objective of the present invention is to extend the strategy and utilize one of the obtained nitro-substituted carbazole product for the total synthesis of natural product staurosporinone in a concise approach.

Another objective of the present invention is the process for the total synthesis of natural products carbazomycin A, calothrixin B and staurosporinone.

SUMMARY OF THE INVENTION

In an embodiment, the present invention provides a carbazoles of general formula (I):

Formula I

wherein‘Ri’ is H, C1-C6 alkyl, benzyl, or allyl; R2 is H, C1-C6 alkyl, cyclopropyl, phenyl, aryl, heteroaryl, C1-C6 methoxy carbonyl, or NO2; R3 is H, C1-C6 alkyl, cyclopropyl, phenyl aryl, heteroaryl, 4-methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, 2-Fluoro phenyl, 4- Fluoro phenyl, or 4-butyl phenyl; R4 is H, benzoyl, -C0₂Et, -CHO, Br, or -OMe; R5 is OH, OMOM, OMe, CN, or OTf; R₆ is H, or O-alkyl; and R₃-R₄ is -CHNCH₂CH₂-.

In an embodiment, the present invention provides, a compound of general formula (II):

Formula (II)

wherein‘Ri’ is H, C1-C6 alkyl, benzyl, or allyl; R3 is H, C1-C6 alkyl, cyclopropyl, phenyl aryl, heteroaryl, 4-methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, or 2-Fluoro phenyl; R₆ is H, or O-alkyl; R3-R4 is -CHNCH2CH2-; and‘X’ is H, F, Cl, I, or Br.

In another embodiment, the present invention provides, process for the preparation of carbazoles of general formula (I) comprising: treatment of indole-ynone of formula (II) , with nitroalkane or substituted nitroalkane of formula (III)

, in the presence of a suitable organic or inorganic base in a suitable polar aprotic solvent at about 80-120 °C for about 10-15 h to obtain compound of Formula I,

Formula I

wherein‘Ri’ is H, C1-C6 alkyl, benzyl, or allyl; R2 is H, C1-C6 alkyl, cyclopropyl, phenyl, aryl, heteroaryl, C1-C6 methoxy carbonyl, or NO2; R3 is H, C1-C6 alkyl, cyclopropyl, phenyl aryl, heteroaryl, 4-methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, 2-Fluoro phenyl, 4- Fluoro phenyl, or 4-butyl phenyl; R4 is H, benzoyl, -CC Et, -CHO, Br, or -OMe; R5 is OH, OMOM, OMe, CN, or OTf; R₆ is H, or O-alkyl; R3-R4 is -CHNCH2CH2-; and‘X’ is H, F, Cl, I, or Br.

In another embodiment, the present invention provides a process for the preparation of carbazomycin A of Formula (1), calothrixin B of Formula (2) and staurosporinone of Formula (3):

carbazomycin A (1 ) calothrixin B (2) staurosporinone (3)

In another embodiment, the present invention provides a process for the preparation of carbazomycin A of Formula (1), calothrixin B of Formula (2) and staurosporinone of Formula (3) involving carbazoles of general formula (I) as an intermediate.

In yet another embodiment, the present invention provides, process for the preparation of carbazomycin A of Formula (1) comprising the following steps:

In yet another embodiment, the present invention provides, process for the preparation of calothrixin B of Formula (2) comprising the following steps:

In yet another embodiment, the present invention provides, process for the preparation of staurosporinone of Formula (3) comprising the following steps:

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides a new and efficient processes and intermediates for the preparation of carbazoles through benzoannulation of indolo-ynones with nitromethane and its derivatives

The present invention relates to the benzoannulation of indolo-ynones with nitroalkane as a one-carbon source to result in serval carbazoles thereof. The invention further relates to the utilization of the above process to obtain the carbazoles and utilize them for the preparation of natural products. The invention also describes the process for the total synthesis of carbazomycin A, calothrixin B and staurosporinone in concise approaches from the carbazoles synthesized.

The strategy of present invention is extended to utilize one of the obtained carbazole product for the total synthesis of natural product, such as, but not limited to: carbazomycin A, calothrixin B and staurosporinone.

As used herein, the modifier "about" should be considered as disclosing the range defined by the absolute values of the two endpoints. For example, the expression "from about 1 to about 4" also discloses the range "from 1 to 4." When used to modify a single number, the term "about" may refer to ±10% of the said number including the indicated number. For example, "about 10% " may cover a range of 9% to 11%, and "about 1" means from 0.9- 1.1.

As used herein, the term“polar aprotic solvents" refers to any organic solvent that lack an acidic hydrogen.

wherein‘Ri’ is H, C1-C6 alkyl, benzyl, or allyl; R2 is H, C1-C6 alkyl, cyclopropyl, phenyl, aryl, heteroaryl, C1-C6 methoxy carbonyl, or NO2; R3 is H, C1-C6 alkyl, cyclopropyl, phenyl aryl, heteroaryl, 4-methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, 2-Fluoro phenyl, 4- Fluoro phenyl, or 4-butyl phenyl; R4 is H, benzoyl, -CC Et, -CHO, Br, or -OMe; R5 is OH, OMOM, OMe, CN, or OTf; R₆ is H, or O-alkyl; and R3-R4 is -CHNCH2CH2-; and the compounds of Formula I are:

9-Methyl-2-phenyl-9H-carbazol-4-ol (6a);

9-Benzyl-2-phenyl-9H-carbazol-4-ol (6b);

9-Allyl-2-phenyl-9H-carbazol-4-ol (6c);

9-Methyl-2-(m-tolyl)-9H-carbazol-4-ol (6d);

2-(4-Ethylphenyl)-9-methyl-9H-carbazol-4-ol (6e);

2-(4-Methoxyphenyl)-9-methyl-9H-carbazol-4-ol (6f);

2-Butyl-9-methyl-9H-carbazol-4-ol (6g);

2-Cyclopropyl-9-methyl-9H-carbazol-4-ol (6h);

6-Methoxy-9-methyl-2-phenyl-9H-carbazol-4-ol (6i);

l,9-Dimethyl-2-phenyl-9H-carbazol-4-ol (6j);

1-Ethyl-9-methyl-2-phenyl-9H-carbazol-4-ol (6k);

Methyl 3-(4-hydroxy-9-methyl-2-phenyl-9H-carbazol-l-yl)propanoate (61);

9-Benzyl- l,2-dimethyl-9H-carbazol-4-ol (6m);

Ethyl 4-hydroxy-9-methyl-2-phenyl-9H-carbazole-3-carboxylate (7a);

Ethyl 2-cyclopropyl-4-hydroxy-9-methyl-9H-carbazole-3-carboxylate (7b);

Ethyl 4-hydroxy-6-methoxy-9-methyl-2-phenyl-9H-carbazole-3-carboxylate (7c); (4-hydroxy-9-methyl-2-phenyl-9H-carbazol-3-yl)(phenyl)methanone (7d);

(2-(2-fluorophenyl)-4-hydroxy-9-methyl-9H-carbazol-3-yl)(phenyl)methanone (7e);

(4-Hydroxy-6-methoxy-9-methyl-2-phenyl-9H-carbazol-3-yl)(phenyl)methanone

(7f);

9-Benzyl- l-nitro-2-phenyl-9H-carbazol-4-ol (8a);

2-(4-Fluorophenyl)-9-methyl-l-nitro-9H-carbazol-4-ol (8b);

2-(4-Butylphenyl)-9-methyl-l-nitro-9H-carbazol-4-ol (8c);

2-Butyl-9-methyl-l-nitro-9H-carbazol-4-ol (8d);

Ethyl 9-benzyl-4-hydroxy-l-nitro-2-phenyl-9H-carbazole-3-carboxylate (8e); Ethyl 2-(4-fluorophenyl)-4-hydroxy-9-methyl-l-nitro-9H-carbazole-3-carboxylate (8f); (4-Hydroxy-9-methyl-l-nitro-2-phenyl-9H-carbazol-3-yl)(phenyl)methanone

(8g);

(2-(4-Butylphenyl)-4-hydroxy-9-methyl-l-nitro-9H-carbazol-3- yl)(phenyl)methanone (8h); and

(2-Cyclopropyl-4-hydroxy-9-methyl-l-nitro-9H-carbazol-3-yl)(phenyl)methanone (8i), etc.

Formula (II)

In another embodiment, the compound of general formula (II) is selected from the group comprising compounds of following formula:

In another embodiment, the present invention provides, process for the preparation of carbazoles of general formula (I) comprising: treatment of indole-ynone of formula (II) with nitroalkane or substituted nitroalkane of formula (III) in the presence of a suitable organic or inorganic base in a suitable polar aprotic solvent at about 80-120 °C for about 10-15 h.

Formula II Formula III Formula I wherein‘Ri’ is H, C1-C6 alkyl, benzyl, or allyl; R3 is H, C1-C6 alkyl, cyclopropyl, phenyl aryl, heteroaryl, 4-methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, or 2-Fluoro phenyl; R₆ is H, or O-alkyl; R3-R4 is -CHNCH2CH2-; and‘X’ is H, F, Cl, I, or Br.

In yet another embodiment, the present invention provides, reaction of the compounds of formula II [where X = H; Ri = C1-C6 alkyl, allyl; benzyl; R3 is C1-C6 alkyl, cyclopropyl, phenyl, aryl; and R6 is H, alkoxy with inorganic base such as K2CO3 or CS2CO3 or Na₂C0₃ in a polar solvents such as DMF or DMSO or Dioxane and heating the mixture along with nitroalkanes of formula III (Where R2 = H, C1-C6 alkyl) at a temperature from about 80-120 °C to provide the compounds of the formula I; wherein Ri = C1-C6 alkyl, allyl; R2 = H, alkyl, R3 is C1-C6 alkyl, cyclopropyl, phenyl, aryl; R4 = H, R5 is OH and R6 is H, alkoxy

In yet another embodiment, the present invention provides, reaction of the compounds of formula II [indolo-ynones, where X = H; Ri = C1-C6 alkyl, allyl; benzyl; R3 is C1-C6 alkyl, cyclopropyl, phenyl, aryl; and R6 is H, alkoxy with inorganic base such as K2CO3 or CS2CO3 or Na₂C0₃ in polar solvents such as DMF or DMSO or dioxane and heating the mixture along with substituted nitroalkane of formula III, wherein R2 = H, Me, alkyl, - CH2CH2COOMe; at a temperature from about 80-120 °C to provide the compounds of the formula I; wherein, Ri is H, methyl, benzyl, and allyl moiety; R2 is H, Me, alkyl, - CH2CH2COOMe, R3 is C1-C6 alkyl, cyclopropyl, phenyl, aryl; R4 is benzoyl, ethoxycarbonyl; R5 is OH, R₆ is alkoxy.

In yet another embodiment, the present invention provides, reaction of the indolo-ynones of formula II [where X = Cl, Ri = C1-C6 alkyl, allyl; benzyl; R₃ is C1-C6 alkyl, cyclopropyl, phenyl, aryl; and R6 is H, alkoxy with inorganic base such as K₂CO₃ or CS₂CO₃ or Na₂C0₃ in polar solvents such as DMF or DMSO or Dioxane, and heating the mixture along with substituted nitrocompound such as benzoylnitromethane or ethylnitroacetate; at a temperature from 80-120 °C to provide the compounds of the formula I; wherein, Ri is H, methyl, benzyl, and allyl moiety; R2 is NO2, R3 is C1-C6 alkyl, cyclopropyl, phenyl, substituted aryl; R4 is H, benzoyl, ethoxycarbonyl; R₅ = OH, and R₆ is alkoxy.

carbazomycin A (1 ) calothrixin B (2) staurosporinone (3)

11 carbazomycin A (1 )

In yet another embodiment, the present invention provides, process for the preparation of carbazomycin A of Formula (1) comprising:

a) O-methylation of compound of Formula (6m) to corresponding methoxy ether of Formula (9); preferably by reacting with methyl iodide or dimethyl sulfate in presence of a suitable base such as, but not limited to, potassium carbonate;

b) bromination of compound of Formula (9) to compound of Formula (10); preferably by reacting with NBS in presence of halogenated solvent such as, but not limited to, chloroform; c) converting compound of Formula (10) to dimethoxy compound of Formula (11), preferably by reacting with sodium methoxide in presence of metal catalyst, such as, but not limited to, copper iodide; and

d) A-dcbcn/ylation of compound of Formula (11) to carbazomycin A of Formula (1); preferably by Pd/C under hydrogen atmosphere.

In yet another embodiment, the present invention also provides the process for the synthesis of carbazole of formula (6m), in particular; and its utility as an intermediate for the total synthesis of carbazomycin A.

calothrixin B (2)

In yet another embodiment, the present invention provides, process for the preparation of calothrixin B of Formula (2) comprising:

a) protecting compound of Formula (8a) to obtain compound of Formula (12); preferably by reacting with MOMC1 in presence of a suitable base such as, but not limited to, triethyl amine and diisopropyl ethyl amine;

b) Cadogan cyclization of compound of Formula (12) to indolocarbazole compound of Formula (13); preferably by reacting with trialkylphosphite or triethylphosphite under monowave condition for half an hour to two hours;

c) Vilsmayer Haack formylation of compound of Formula (13) to aldehyde of Formula (14); d) protecting compound of Formula (14) to obtain compound of Formula (15); preferably by reacting with MOMC1 in presence of diisopropyl ethyl amine;

e) converting compound of Formula (15) to phenanthridine compound of Formula (16) by one-pot oxidative deprotection and intramolecular imine formation; and

f) N-debenzylation of compound of Formula (16) to calothrixin B of Formula (2); preferably by reacting with AlCb in anisole.

The invention also provides the process for the synthesis of carbazole (8a), in particular; and its utility as an intermediate for the total synthesis of calothrixin B.

staurosporinone (3)

In yet another embodiment, the present invention provides, process for the preparation of staurosporinone of Formula (3) comprising:

a) Benzoannulation of chloro substituted /V-benzylated indole-ynone of Formula (41); preferably by reacting with ethyl nitroacetate and CS2CO3 as a base in a suitable polar solvent such as DMF at 80-120 °C temperature for a period of 6-12 h to obtain compound 8e;

b) converting compound of Formula (8e) to triflate compound of Formula (17); preferably by reacting with triflic anhydride in presence of pyridine at 0°C to room temperature for 2-6 h; c) cyanation of compound of Formula (17) to compound of Formula (18); preferably by reacting with zinc cyanide in presence of metal catalyst such as tetrakistriphenyl phosphine and salf copper iodide in presence of polar solvent such as DMF at 110-140 °C for a period of d) Cadogen cyclization of compound of Formula (18) to compound of Formula (19); preferably by reacting with trialkylphosphite, such as, but not limited to triethylphosphite, under monowave condition for half an hour to two hours at 180-200 °C;

e) converting compound of Formula (19) to /V-benzylated staurosporinone of Formula (20); preferably by reacting with Raney Nickel in polar solvent, such as, but not limited to isopropanol, tert.butanol, DMF, methanol and DMF or mixture thereof under hydrogen atmosphere at room 20-40 °C for 36-48 h; and

f) debenzylation of compound of Formula (20) to staurosporinone of Formula (3); preferably by reacting with AlCb in presence of anisole at 0-110 °C for 30 min. to 2 h.

The invention also provides the process for the synthesis of carbazole (8e), in particular; and its utility as an intermediate for the total synthesis of staurosporinone.

LIST OF ABBREVIATIONS

HPLC = High pressure Liquid chromatography

TLC = Thin layer chromatography

NMR = Nuclear Magnetic resonance

UV = Ultra-Violet

HRMS = High resolution mass spectroscopy

GC = Gas chromatography

IR = Infra-red

DCM = Dichloromethane

CAN: Ceric ammonium nitrate

THF: tetrahydrofuran

DCM: dichloromethane

MOM = methoxymethyl

MATERIAL AND METHOD USED IN EXPERIMENTS

Most of the reagents and chemicals used in the process are bought from Spectrochem, AVRA or Sigma-Aldrich, which were used as such without any further purification. Common organic chemicals and salts were purchased from AVRA chemicals, India.

All work-up and purification procedures were carried out with reagent-grade solvents. Analytical thin-layer chromatography (TLC) was performed using analytical chromatography silica gel 60 F254 precoated plates (0.25 mm). The developed chromatogram was analysed by UV lamp (254 nm) and by charring in solutions of anisaldehyde or □-naphtol. The reaction steps were monitored by thin layer chromatography and the crude products obtained were subjected to purification by column chromatography or crystallization or extraction or filtration to get the pure compounds. All the resultant products were characterized using available analytical and spectral methods.

In these processes, all the reaction steps were monitored by thin layer chromatography and the crude products obtained were subjected to purification using crystallization or chromatography using silica gel (60-120 or 100-200 mesh) mixture of polar and non-polar solvents as mobile phase to get the pure compounds in good yields. Further, all the resultant compounds/products were systematically characterized using various analytical and spectral methods.

Measurement Method

High-resolution mass spectra (HRMS) were obtained from a JMS-T100TD instrument (DART) and Thermo Fisher Scientific Exactive (APCI).

Nuclear magnetic resonance (NMR) spectra were recorded on a Bruker 600, 500, 400 or 300 MHz in CDCb or DMSO-d₆ solvent. Chemical shifts for ¹ H NMR are expressed in parts per million (ppm) relative to tetramethylsilane (d 0.00 ppm). Chemical shifts for ¹³C NMR are expressed in ppm relative to CDCI3 (d 77.0 ppm). Data are reported as follows: chemical shift, multiplicity (s = singlet, d = doublet, dd = doublet of doublets, t = triplet, q = quartet, quin = quintet, sext = sextet, m = multiplet), coupling constant (Hz), and integration.

EXAMPLES

Following examples are given by way of illustration and therefore should not be construed to limit the scope of the invention.

9-Methyl-2-phenyl-9H-carbazol-4-ol (6a);

9-Benzyl-2-phenyl-9H-carbazol-4-ol (6b);

9-Allyl-2-phenyl-9H-carbazol-4-ol (6c);

9-Methyl-2-(m-tolyl)-9H-carbazol-4-ol (6d);

2-(4-Ethylphenyl)-9-methyl-9H-carbazol-4-ol (6e);

2-(4-Methoxyphenyl)-9-methyl-9H-carbazol-4-ol (6f);

2-Butyl-9-methyl-9H-carbazol-4-ol (6g);

2-Cyclopropyl-9-methyl-9H-carbazol-4-ol (6h); 6-Methoxy-9-methyl-2-phenyl-9H-carbazol-4-ol (6i);

l,9-Dimethyl-2-phenyl-9H-carbazol-4-ol (6j);

1-Ethyl-9-methyl-2-phenyl-9H-carbazol-4-ol (6k);

Methyl 3-(4-hydroxy-9-methyl-2-phenyl-9H-carbazol-l-yl)propanoate (61);

9-Benzyl- l,2-dimethyl-9H-carbazol-4-ol (6m);

Ethyl 4-hydroxy-9-methyl-2-phenyl-9H-carbazole-3-carboxylate (7a);

Ethyl 2-cyclopropyl-4-hydroxy-9-methyl-9H-carbazole-3-carboxylate (7b);

(2-(2-fluorophenyl)-4-hydroxy-9-methyl-9H-carbazol-3-yl)(phenyl)methanone (7e);

(4-Hydroxy-6-methoxy-9-methyl-2-phenyl-9H-carbazol-3-yl)(phenyl)methanone

(7f);

9-Benzyl- l-nitro-2-phenyl-9H-carbazol-4-ol (8a);

2-(4-Fluorophenyl)-9-methyl-l-nitro-9H-carbazol-4-ol (8b);

2-(4-Butylphenyl)-9-methyl-l-nitro-9H-carbazol-4-ol (8c);

2-Butyl-9-methyl-l-nitro-9H-carbazol-4-ol (8d);

Ethyl 9-benzyl-4-hydroxy-l-nitro-2-phenyl-9H-carbazole-3-carboxylate (8e); Ethyl 2-(4-fluorophenyl)-4-hydroxy-9-methyl- l-nitro-9H-carbazole-3-carboxylate (8f);

(4-Hydroxy-9-methyl-l-nitro-2-phenyl-9H-carbazol-3-yl)(phenyl)methanone

(8g);

(2-(4-Butylphenyl)-4-hydroxy-9-methyl-l-nitro-9H-carbazol-3- yl)(phenyl)methanone (8h);

(2-Cyclopropyl-4-hydroxy-9-methyl-l-nitro-9H-carbazol-3-yl)(phenyl)methanone (8i) etc.

In another embodiment, the representative compounds of Formula (I) are:

Procedure for the preparation of compounds of formula I (6a-6m), (7a-7f) and (8a-8i).

R 1 R

Formula II Formula I II Formula I

General procedure 1 : In an oven dried Ace pressure tube was taken indole-ynone (0.1 mmol) and nitromethane (0.3 mmol) and to this DMF (2 mL) and CS2CO3 (0.2 mmol) were added and the cap was closed tightly, placed in a preheated oil bath at 100 °C and stirred for 12 h at the same temperature. The reaction mixture was cooled to room temperature and diluted with cold H2O (5 mL) and extracted with EtOAc (3 x 5 mL). The combined organic extract was washed with brine (10 mL) and dried over anhydrous Na₂S0₄; volatiles were removed under reduced pressure to get the crude compound which was purified by silica gel flash column chromatography (EtO Ac/Hexane) to give carbazoles (6a-6m, 7a-7f, 8a-8i). Example 1: 9-Methyl-2-phenyl-9H-carbazol-4-ol (6a):

In an oven dried Ace pressure tube were taken indole-ynone 4a (0.1 mmol) and nitromethane (0.3 mmol) and to this DMF (2 mL) and CS2CO3 (0.2 mmol) were added and the cap was closed tightly, placed in a preheated oil bath at 100 °C and stirred for 12 h at the same temperature. The reaction mixture was cooled to room temperature and diluted with cold H2O (5 mL) and extracted with EtOAc (3 x 5 mL). The combined organic extract was washed with brine (10 mL) and dried over anhydrous Na₂S0₄; volatiles were removed under reduced pressure to get the crude compound which was purified by silica gel flash column chromatography (EtOAc/Hexane) to give carbazole 6a as pale brown solid (24.0 mg, 88%); R/= 0.4 (20% EtOAc + Hexane); mp 166-168

8.27 (d, / = 7.7 Hz, 1H), 7.69 - 7.63 (m, 2H), 7.48 - 7.42 (m, 3H), 7.38 - 7.32 (m, 2H), 7.28 - 7.22 (m, 1H), 7.16 (d, / = 1.2 Hz, 1H), 6.78 (d, / = 1.2 Hz, 1H), 5.41 (s, 1H), 3.82 (s, 3H); ¹³C NMR (101 MHz, CDCL) d 151.8, 143.4, 141.9, 140.9, 140.3, 128.8, 127.6, 127.3, 125.0, 122.7, 121.7, 119.4, 110.3, 108.1, 104.6, 100.3, 29.4; IR (neat): D_max 641, 699, 756, 833, 922,

1156, 1263, 1329, 1489, 1601, 1634, 3051, 3472 cm^{r l}; HRMS (ESIMS) calcd. for C_I9H_I6NO [M+H]⁺: calcd m/z 274.1233; found: 274.1232.

The compounds of formula 6b to 6m were synthesized following the procedure described above under example 1 and general procedure involving 4a-4j corresponding reactants of formula II and nitromethane (for 6a-6i), 4a with nitroethane for 6j, 4a with nitropropane for 6k, 4a with 3-nitromethyl butyrate for 61, and 4j with nitroethane for 6m.

Reactants of formula II used for the synthesis of 6b-6m

In another embodiment, the representative compounds of Formula I are:

The compound of formula (7a)-(7c) were synthesized following the procedure described above under example 1 and general procedure involving 4a, 4h, and 4i respectively corresponding reactants of formula II and ethylnitroacetate. The compound of formula (7d)- (7f) were synthesized following the procedure described above under example 1 and general procedure involving 4a, 4k, and 4i respectively corresponding reactants of formula II and benzoylnitromethane.

In yet another embodiment, the present invention provides access to nitro substituted carbazoles of formula I starting from chloro substituted indole-ynones on reaction with nitroalkane and substituted nitroalkanes.

X = Halogen Formula I

In another embodiment, the representative compounds of Formula I with nitro substitution are:

The compound of formula (8a)-(8h) was synthesized following the procedure described above under example 1 and general procedure involving corresponding reactants of formula II and nitromethane or ethylnitroacetate or benzoyl nitromethane.

The invention also provides concise approach for the total synthesis of carbazomycin A from one of the above obtained products of formula I (6m) and is described as follows:

The carbazomycin A is isolated from streptromyces ehimense H 1051 -MY by Nakamura et al in 1980 and was found to display potent antibiotic properties. It is a structurally diverse 3,4- dioxygenated carbazole alkaloid. This newly developed process starts from four step sequence from the carbazole (6m) obtained via the new process employing benzoannulation of indole- alkynone with nitromethane. The present process can be performed very effectively in concise manner and in highly viable strategy which could be the most suitable for its large scale production of carbazomycin.

In yet another embodiment, the present invention provides, the preparation of carbazomycin A, comprising of four-step sequence starting from (6m) comprising of required dimethyl substitutions obtained from our process as described earlier. As a requisite, the phenolic hydroxy in 6m was protected as the corresponding methoxy ether 9 with dimethyl sulfate in presence of potassium carbonate. The compound (9) was then subjected to bromination with NBS in halogenated solvent in particular chloroform to get the brominated product (10). Treatment of aryl bromide (10) with sodium methoxide in presence of copper iodide furnished the dimethoxy product (11). Finally, compound (11) on A-dcbcnzylation with Pd/C provided the target compound carbazomycin (A). The data of the synthesized product was found to be identical as that of the reported data for the natural product. The structure was also determined by its single crystal X-ray structure.

Example 28: 9-Benzyl-4-methoxy-l,2-dimethyl-9H-carbazole (9): To a stirring solution of carbazole 6m (151.0 mg, 0.5 mmol) in anhydrous acetone (5.0 mL) were added K2CO3 (104.0 mg, 0.75 mmol) and Me₂S0₄ (76 mg, 0.6 mmol). The resulting reaction mixture was heated at 80 °C for 3 h. After completion of the reaction, it was filtered through a short plug of celite and the filtrate was concentrated in rotavapour and purified by silica gel column chromatography to afford the methoxy protected carbazole 9 as pale yellow solid (151.0 mg, 96%). R = 0.3 (20% EtOAc + Hexane);

8.36 - 8.32 (m, 1H), 7.34 - 7.16 (m, 6H), 7.09 - 7.02 (m, 2H), 6.55 (s, 1H), 5.70 (s, 2H), 4.05 (s, 3H), 2.41 (s, 3H), 2.41 (s, 3H); ¹³C NMR (101 MHz, CDCb) d 153.8, 141.4, 141.3, 139.0, 135.5, 128.9, 127.1, 125.7, 124.6, 122.8, 122.6, 119.6, 111.7, 111.1, 108.4, 103.7, 55.4, 48.8, 21.6, 14.2; IR (neat): D_max 730, 996, 1165, 1223, 1327, 1456, 1591, 2841, 2959 cm ¹; HRMS (ESIMS) calcd. for C22H22NO [M+H]⁺: calcd m/z 316.1701; found: 316.1699. Example 29: 9-Benzyl-3-bromo-4-methoxy-l,2-dimethyl-9H-carbazole (10): To a stirring solution of carbazole 7 (100.0 mg, 0.32 mmol) in CHCb (10 mL) at room temperature was added NBS (57.0 mg, 0.32 mmol) and stirred for 5 min, after completion of the reaction (monitored by TLC), the mixture was diluted with CH2CI2 (10 mL) and H2O (10 mL). Layers were separated and the aqueous layer was extracted with CH2CI2 (2 x 5 mL), the combined organic extract was dried over Na2S04, volatiles were removed under reduced pressure and the resulted crude compound was purified by silica gel column chromatography to afford the bromo-carbazole 10 as yellow solid (105.6 mg, 84%). R_f = 0.5 (20% EtOAc + Hexane);¹!! NMR (400 MHz, CDCL) d 8.28 (d, / = 7.7 Hz, 1H), 7.39 (ddd, / = 8.3, 7.3, 1.2 Hz, 1H), 7.32 - 7.19 (m, 5H), 7.08 (d, / = 6.8 Hz, 2H), 5.66 (s, 2H), 4.06 (s, 3H), 2.54 (s, 3H), 2.51 (s, 3H); ¹³C NMR (101 MHz, CDCL) d 150.3, 142.2, 140.6, 138.4, 134.8, 129.0, 127.3, 125.9, 125.6, 122.6, 121.2, 120.2, 116.4, 111.2, 109.0, 60.1, 49.2, 20.8, 16.0; IR (neat): D_max 751, 814, 1043, 1161, 1248, 1356, 1386, 1583, 2933 cm ¹; HRMS (ESIMS) calcd. For C₂2H_2iNOBr [M+H]⁺: calcd m/z 394.0807; found: 394.0807.

Example 30: 9-Benzyl-3,4-dimethoxy-l,2-dimethyl-9H-carbazole (11): To a freshly prepared solution of NaOMe in MeOH were added bromo-carbazole 10 (100.0 mg, 0.25 mmol) in DMF (3.0 mL), Cul and the reaction mixture was heated at 120 °C for 18 h. After completion of the reaction filtered through a short plug of celite using EtOAC and the solution was washed with cold water, brine. The organic layer was dried over NaiSCL, volatiles were removed under reduced pressure and the resulted crude compound was purified by silica gel column chromatography to afford the dimethoxy-carbazole 11 as off white solid (72.0 mg,

8.32 (d, / = 7.6 Hz, 1H), 7.37-7.19 (m, 6H), 7.11 (d, J = 7.1 Hz, 2H), 5.68 (s, 2H), 4.13 (s, 3H), 3.89 (s, 3H), 2.45 (s, 3H), 2.34 (s, 3H); ¹³C NMR (101 MHz, CDCL) d 146.0, 144.4, 142.2, 138.9, 137.5, 129.9, 128.9, 127.2, 125.7, 125.3, 122.5, 122.2, 119.5, 115.7, 114.8, 108.7, 61.0, 60.4, 49.1, 15.0, 13.1; IR (neat): D_max 744, 1087, 1213, 1506, 1540, 1650, 2356, 3158 cm ¹; HRMS (ESIMS) calcd. for C23H24NO2 [M+H]⁺: calcd m/z 346.1079; found: 346.1069.

Example 31: 3,4-dimethoxy-l,2-dimethyl-9H-carbazole (carbazomycin A) (1): To a solution of benzyl compound 11 (50.0 mg) in MeOH (5.0 mL) was added 10% Pd/C (50 mg) and hydrogen balloon pressure was applied and stirred for 6 h. After completion of the reaction, as indicated by the TLC, filtered through a short plug of silica gel with the aid of EtOAc. Volatiles were removed under reduced pressure and the resulted crude compound was purified by column chromatography afforded the natural product carbazomycin A (1), as pale brown solid (37.0 mg, 92%); NMR (400 MHz, CDCL) d 8.23 (d, / = 7.8 Hz, 1H), 7.81 (s, 1H), 7.44 - 7.33 (m, 2H), 7.21 (t, / = 7.3 Hz, 1H), 4.10 (s, 3H), 3.89 (s, 3H), 2.41 (s, 3H), 2.38 (s, 3H); ¹³C NMR (101 MHz, CDCh) d 146.0, 144.5, 139.4, 136.5, 128.8, 125.1, 122.9, 122.6, 119.5, 114.5, 113.5, 110.3, 61.1, 60.6, 13.7, 12.7. IR (neat): D_max 1034, 1302, 1480, 2975, 3435 cm ¹; HRMS (ESIMS) calcd. For CieHisNOi [M+H]⁺: calcd m/z 256.0974; found: 256.0968.

The invention also provides concise approach for the total synthesis of calothrixin B from one of the above obtained products of formula I as the starting material and is described as follows:

The unique pentacyclic alkaloid, calothrixin B is isolated from calothrix cyanobacteria and is found to display antimalarial and antiproliferative properties. This natural product is synthesized from the substituted carbazole 8a obtained from the new process of benzoannulation of chlorosubstituted indole-ynone and nitromethane.

In yet another embodiment, the present invention provides the preparation of calothrixin B, comprising of six step synthesis starting from (8a).

Thus, (8a) was treated with MOMC1 and DIPEA to get the corresponding MOM ether (12). The compound (12) was subjected to Cadogan cyclization upon treatment with thiethylpho shite under monowave condition to deliver the indolocarbazole (13). Compound (13) was subjected to Vilsmeier-Haack formylation reaction to get the aldehyde (14). The secondary amine in (14) was protected as the corresponding MOM derivative (15) with DIPEA and MOMC1 in 88% yield. Cericammonium nitrate (CAN) mediated one -pot oxidative deprotection of MOM groups in (15) and further intramolecular cyclization of resulting free N¾ and aldehyde provided the known phenanthridine moiety (16). The compound 16 was subjected to the process of debenzylation known in the prior art with AlCb in anisole to yield A-dcbcnzylatcd target natural product calothrixin B in decent yield. The data of the synthesized product was in good agreement with that of the reported data of natural product.

Example 32: 9-Benzyl-4-(methoxymethoxy)-l-nitro-2-phenyl-9H-carbazole (12): To a stirring solution of carbazole 8a (mmol) in dichloromethane at 0 °C were added DIPEA (mmol) and MOMC1, the solution was warmed to room temperature and stirred for 3 h. After completion of the reaction as indicated by TLC, diluted with dichloromethane and H2O, layers were separated and the aqueous layer was extracted with dichloromethane (3 x 10 mL). The combined organic layer was dried over NaiSCC and volatiles were removed under reduced pressure to give the crude compound, which was purified by silica gel column chromatography to afford the MOM compound 12 as bright yellow soild (152 mg, 91%). mp 153-154 °C. R/= 0.5 (20% EtOAc + Hexane); NMR (500 MHz, CDCb) d 8.44 (d, 7 = 7.8 Hz, 1H), 7.48 (ddd, 7 = 8.3, 7.2, 1.2 Hz, 1H), 7.37 (dddd, 7 = 14.9, 11.9, 6.9, 2.0 Hz, 7H), 7.24 - 7.16 (m, 3H), 7.05 - 6.98 (m, 2H), 6.88 (s, 1H), 5.52 (s, 2H), 5.46 (s, 2H), 3.60 (s, 3H); ¹³C NMR (126 MHz, CDCb) d 153.7, 141.8, 137.9, 136.6, 134.7, 132.1, 130.7, 128.7, 128.5, 128.3, 128.2, 127.6, 126.6, 126.1, 123.4, 121.3, 121.1, 114.9, 109.5, 107.0, 94.6, 56.7, 47.7; HRMS (ESIMS) calcd. For C27H23N2O4 [M+H]⁺: calcd m/z 439.1658; found: 439.1647.

Example 33: 12-Benzyl-5-(methoxymethoxy)-l l,12-dihydroindolo[2,3-a]carbazole (13): In a 10 mL monowave glass vial, compound 12 (120 mg) was taken in 1,2-dichlorobenzene (1 mL) and added triethylphosphite (1 mL), closed with silicone cap and heated up to 180 °C for 180 min (2x90 min) in monowave 50 (Anton paar) reactor. The reaction mixture was purified by column chromatography (15% EtOAc + Hexane) to afford indolo-carbazole 13 as dark brown solid (83 mg, 75%). mp 144-145 °C. R/ = 0.3 (20% EtOAc + Hexane);

NMR (500 MHz, DMSO) d 11.36 (s, 1H), 8.37 (d, 7 = 7.7 Hz, 1H), 8.13 (d, 7 = 7.8 Hz, 1H), 7.62 (t, 7 = 4.1 Hz, 2H), 7.57 (d, 7 = 8.1 Hz, 1H), 7.42 - 7.34 (m, 2H), 7.28 - 7.15 (m, 7H), 6.11 (s, 2H), 5.60 (s, 2H), 3.56 (s, 3H). ¹³C NMR (126 MHz, DMSO) d 147.53, 140.57, 139.67, 138.90, 129.06, 128.02, 127.70, 127.15, 125.24, 124.75, 123.66, 123.31, 122.62, 122.06, 120.80, 120.09, 119.22, 112.08, 111.88, 110.23, 95.87, 95.00, 56.42, 47.78.; IR (neat): D_max 753, 1019, 1156, 1454, 2948, 3422, 3885 cm ¹; HRMS (ESIMS) calcd. For C27H23N2O2 [M+H]⁺: calcd m/z 407.1760; found: 407.1751.

l l-Benzyl-6-(methoxymethoxy)-12-(methoxymethyl)-l l,12-dihydroindolo[2,3-a]carbazole- 5-carbaldehyde (15): To a stirring solution of DMF and POCI3 at 0 °C was added indolo- carbazole 13 in DMF. The reaction mixture was warmed to room temperature and stirred for 3 h. After completion of the reaction diluted with water and EtOAc, layers were separated and aqueous layer was extracted with EtOAc (3 x 10 mL). The combined organic extract was washed with sat. NaHC0₃ solution and dried over Na₂S0₄, volatiles were removed under reduced pressure gave crude compound, which was purified by silica gel flash column chromatography to afford the aldehyde compound 14. This compound was directly subjected to N-MOM protection. To a stirring solution of aldehyde 14 (mmol) in dichloromethane at 0 °C were added DIPEA (mmol) and MOMC1, the solution was warmed to room temperature and stirred for 3 h. After completion of the reaction as indicated by TLC, diluted with dichloromethane and H2O, layers were separated and the aqueous layer was extracted with dichloromethane (3 x 10 mL). The combined organic layer was dried over Na₂S0₄ and volatiles were removed under reduced pressure to give the crude compound, which was purified by silica gel column chromatography to afford the di-MOM compound 15 as pale brown solid (70 mg, 85%); R/ = 0.5 (20% EtOAc + Hexane); mp 130-132 °C;

NMR (400 MHz, CDCb) d 10.91 (s, 1H), 9.17 (d, / = 8.2 Hz, 1H), 8.45 - 8.32 (m, 1H), 7.56 - 7.47 (m, 2H), 7.45 - 7.31 (m, 8H), 7.24 - 7.17 (m, 1H), 5.86 (s, 2H), 5.46 (s, 2H), 5.22 (s, 2H), 3.70 (s, 3H), 2.89 (s, 3H). ¹³C NMR (101 MHz, CDCb) d 190.64, 154.53, 145.28, 143.35, 136.95, 134.47, 129.02, 127.61, 127.15, 126.26, 126.22, 126.01, 125.75, 124.97, 123.51, 122.58, 122.17, 122.01, 121.58, 118.99, 116.46, 111.82, 110.84, 101.65, 79.24, 58.60, 55.35, 50.80; IR (neat): D_max 752, 962, 1078, 1172, 1256, 1336, 1449, 1600, 1716, 2938 cm ¹; HRMS (ESIMS) calcd. For C30H27N2O4 [M+H]⁺: calcd m/z 479.1971; found: 479.1966.

12-Benzyl-7H-indolo[3,2-j]phenanthridine-7,13(12H)-dione (16): To a solution of diMOM compound 15 (50 mg, 0.1 mmol) in 1 mL of acetonitrile and H2O (10:1) was added CAN (cerium ammonium nitrate, 165 mg, 0.3 mmol) and the reaction mixture was stirred at room temperature for 14 h. After completion of the reaction diluted with EtOAc (10 mL) and H2O (5 mL), layers were separated; the aqueous layer was extracted with EtOAc (3 x 5 mL). The combined organic extract was washed with IN NaOH (5 mL), the resulted organic layer was dried over Na2S04 and volatiles were removed under reduced pressure to give crude compound, which upon purification by silica gel column chromatography (15% EtOAc + Hexane) afforded the di-MOM compound 16 as orange solid (28 mg, 69%) (compound known in the prior art (Org. Lett. 2017, 19, 2785-2788); mp 262-263 °C; R/ = 0.4 (20% EtOAc + Hexane);

NMR (500 MHz, CDCI3) d 9.79 (s, 1H), 9.54 (d, / = 8.7 Hz, 1H), 8.45 (d, / = 7.3 Hz, 1H), 8.18 (d, / = 8.3 Hz, 1H), 7.86 - 7.78 (m, 1H), 7.77 - 7.68 (m, 1H), 7.50 -

7.38 (m, 3H), 7.36 - 7.18 (m, 5H), 6.00 (s, 2H); ¹³C NMR (126 MHz, CDCI3) d 182.06,

181.07, 152.20, 147.92, 140.17, 136.25, 135.19, 133.33, 131.43, 130.38, 130.15, 128.95,

128.05, 127.91, 127.72, 126.64, 125.21, 124.53, 123.98, 123.34, 123.18, 117.75, 111.61,

48.59; IR (neat): D_max 764, 1302, 1461, 1708, 2855, 2923 cm ¹; HRMS (ESIMS) calcd. For C26H17N2O2 [M+H]⁺: calcd m/z 389.1290; found: 389.1284.

7H-Indolo[3,2-j]phenanthridine-7,13(12H)-dione, Calothrixin B 3 (2):

To a solution of AICI3 (65 mg, 0.5 mmol) in anisole (0.5 mL) at 0 °C was added a solution of compound 16 (20 mg, 0.05 mmol) in anisole (0.5 mL), the reaction mixture was heated at 80 °C for 8 h. After completion of the reaction (by TLC) cooled to room temperature, filtered through celite with the aid of EtOAc and the volatiles were removed under reduced pressure and the crude compound was purified by column chromatography (20% EtOAc + Hexane) to afford calothrixin B, 3 as orange solid (Org. Lett. 2017, 19, 2785-2788). (10.7 mg, 72%). R/ = 0.3 (20% EtOAc + Hexane); mp 298-300 °C; ¾ NMR (400 MHz, DMSO) d 13.16 (s, 1H), 9.63 (s, 1H), 9.59 (d, J = 8.6 Hz, 1H), 8.18 (dd, J = 7.7, 4.6 Hz, 2H), 8.00 - 7.93 (m, 1H), 7.93 - 7.86 (m, 1H), 7.63 (d, / = 8.2 Hz, 1H), 7.51 - 7.45 (m, 1H), 7.40 (t, J = 1.1 Hz, 1H); ¹³C NMR (101 MHz, DMSO) d 180.9, 180.4, 151.2, 147.5, 138.4, 138.1, 132.7, 131.6, 130.3, 129.8, 127.2, 127.2, 124.9, 124.3, 123.7, 122.6, 122.3, 115.5, 114.0; IR (neat): D_max 987, 1076, 1437, 1648, 2949, 3458 cm ¹; HRMS (ESIMS) calcd. For C19H11N2O2 [M+H]⁺: calcd m/z 299.0821; found: 299.0819.

The invention also provides concise approach for the total synthesis of staurosporinone from one of the above obtained products 8e of formula III as the starting material and is described as follows:

The indolocarbazole alkaloid k-252c named as staurosporinone was isolated in 1986 from culture broths of Nocardiopsis sp K-252 and Nocardiopsis Sp. K-290. This compound is known to be potent inhibitor of protein kinase C. The aglycone of staurosporine, staurosporinone has attracted significant attention from chemists because of the interesting biological activity and novel functional pattern of the hexasubstituted arene framework. Some of the key synthetic methods for its preparation from literature involve metal catalyzed C-H amination and C-H carbonylation reactions along with several other key reactions. The natural product is prepared starting from nitro-substituted carbazole synthesized from our developed process in further five simple steps.

In yet another embodiment, the present invention provides the preparation of staurosporinone starting from carbazole 8e synthesized earlier and comprises of five step sequence.

Accordingly, the phenolic hydroxy in compound 8e was activated by converting it to triflate 17 and then treated with zinc cyanide in presence of copper (II) iodide and tetrakistriphenylphosphine palladium to afford the cyanated nitro carbazole 18. Cadagon cyclization of 18 with triethylphosphite under monowave conditions delivered the pentacyclic indolocarbazole 19. One-pot reduction of cyanide to amine followed by lactam formation with adjacent ester moiety was achieved with Raney Ni in DMF and methanol as solvent from 19 leading to the core skeleton 20 with benzyl appendage on nitrogen atom of staurosporinone. Finally, /V-debenzylation of 20 with AICI₃ in anisole furnished the target natural product in good yield. The analytical data of the synthesized product was in good agreement with that of the data of the reported natural product. Example 34: Ethyl 9-benzyl- l-nitro-2-phenyl-4-(((trifluoromethyl)sulfonyl)oxy)-9H- carbazole-3-carboxylate (17): To a stirring solution of carbazole 8e (150.0 mg, 0.32 mmol) in dichloromethane (5.0 mL) at 0 °C were added pyridine (40.0 DL, 0.48 mmol) and TEO (70.0 □ L, 0.42 mmol), the reaction was warmed to room temperature and was allowed to stir for 3 h. After completion of the reaction (monitored by TLC) it was diluted with dichloromethane (5.0 mL), quenched by the addition of sat.aq. NaHCCE (1.0 mL), H2O (5.0 mL), layers were separated and the aqueous layer was extracted with dichloromethane (2 x 5 mL). The combined organic extract was dried over NaiSCri and the volatiles were removed under reduced pressure to give the crude compound, which was purified by silica gel column chromatography (25% EtOAc + Hexane) to yield the triflate compound 17 as pale yellow solid (177.0 mg, 92%). R/ = 0.5 (40% EtOAc + Hexane); mp: 145-147 °C;

NMR (400 MHz, CDCI3) d 8.46 (d, / = 8.0 Hz, 1H), 7.65 - 7.59 (m, 1H), 7.49 - 7.43 (m, 2H), 7.40 - 7.33 (m, 3H), 7.30 (dt, / = 3.8, 2.1 Hz, 2H), 7.27 - 7.22 (m, 3H), 6.98 (dd, / = 6.8, 2.8 Hz, 2H), 5.44 (s, 2H), 3.95 (q, / = 7.2 Hz, 2H), 0.86 (t, / = 7.2 Hz, 3H); ¹³C NMR (101 MHz, CDCb) d 163.9, 142.7, 139.9, 135.4, 133.7, 132.6, 131.8, 129.2, 129.0, 129.9, 128.9, 128.2, 128.0, 127.6, 125.7, 123.4, 122.4, 120.2, 119.7, 119.2, 110.4, 62.0, 47.6, 13.3; IR (neat): D_max 751, 841, 1233, 1377, 1488, 1595, 2201 cm ¹; HRMS (ESIMS) calcd. Lor C29H22N2O7L3S [M+H]⁺: calcd m/z 599.1100; found: 599.1108.

Example 35: Ethyl 9-benzyl-4-cyano-l-nitro-2-phenyl-9H-carbazole-3-carboxylate (18): To a stirring solution of triflate 17 (150.0 mg, 0.25 mmol) in DML (3.0 mL) were added Pd(PPh3)4 (29.0 mg, 0.025) and Zn(CN)₂ (88.0 mg, 0.75 mmol), the reaction mixture was heated at 120 °C for 18 h. After completion of the reaction, solids were filtered, the filtrate was diluted with cold H2O and was extracted with EtOAc (3 x 5 mL), the combined organic extract was dried over Na2S04 and volatiles were removed under reduced pressure to give the crude compound, which was purified by silica gel column chromatography (30% EtOAc + Hexane) to afford the cyano compound 18 as orange solid (102.0 mg, 86%). R/ = 0.3 (40% EtOAc + Hexane); mp: 188-190 °C;

NMR (500 MHz, CDCb) d 8.83 (d, / = 8.0 Hz, 1H), 7.70 - 7.61 (m, 1H), 7.51 - 7.45 (m, 2H), 7.42 - 7.34 (m, 3H), 7.31 - 7.28 (m, 2H), 7.24 (dt, J = 6.8, 2.8 Hz, 3H), 6.98 - 6.93 (m, 2H), 5.45 (s, 2H), 4.12 (q, / = 7.1 Hz, 2H), 1.00 (t, J = 7.1 Hz, 3H); ¹³C NMR (126 MHz, CDCb) d 165.2, 143.4, 137.6, 135.3, 133.2, 131.3, 130.0, 129.9, 129.5, 129.2, 128.9, 128.30 128.1, 127.3, 125.7, 122.5, 122.4, 120.0, 115.7, 110.4, 104.8, 62.5, 47.5, 13.5; IR (neat): D_max 751, 1222, 1267, 1538, 1728, 2231 cm ; HRMS (ESIMS) calcd. For C29H22N3O4 [M+H]⁺: calcd m/z 476.1610; found: 476.1591. Example 36: Ethyl l l-benzyl-6-cyano-l l,12-dihydroindolo[2,3-a]carbazole-5-carboxylate

(19): In a 10 mL monowave glass vial, compound 18 (100.0 mg) was taken in 1,2- dichlorobenzene (0.5 mL) and added triethylphosphite (0.5 mL), closed with silicone cap and heated up to 180 °C for 180 min (2 x 90 min) in monowave 50 (Anton paar) reactor. After completion of the reaction it was directly purified by column chromatography (25-35% EtOAc + Hexane) to afford indolo-carbazole 19 as light brown solid (70.0 mg, 75%) and 27 (20 mg, 19%). R f = 0.5 (50% EtOAc + Hexane); mp: 282-282

DMSO) d 12.27 (s, 1H), 8.64 (d, 7 = 8.0 Hz, 1H), 8.09 (d, 7 = 8.1 Hz, 1H), 7.81 (d, 7 = 8.3 Hz, 1H), 7.75 (d, 7 = 8.1 Hz, 1H), 7.57 (dt, 7 = 14.8, 7.4 Hz, 2H), 7.43 (t, 7 = 7.5 Hz, 1H), 7.33 (t, 7 = 7.5 Hz, 1H), 7.19 (ddd, 7 = 25.5, 16.1, 6.9 Hz, 5H), 6.24 (s, 2H), 4.68 (q, 7 = 7.1 Hz, 2H), 1.49 (t, 7 = 7.1 Hz, 3H); ¹³C NMR (101 MHz, DMSO) d 167.2, 141.2, 141.1, 138.1, 129.2, 127.9, 127.6, 127.5, 127.3, 127.0, 124.5, 122.0, 121.7, 121.4, 121.1, 121.0, 120.6, 119.12, 118.5, 118.4, 112.9, 111.6, 93.8, 62.8, 48.0, 14.4; IR (neat): □_max 758, 1024, 1226, 1458, 1542, 1731, 2857, 2925 cm ¹; HRMS (ESIMS) calcd. For C29H22N3O2 [M+H]⁺: calcd m/z 444.1712; found: 444.1703.

Example 37: 12-Benzyl-6,7,12,13-tetrahydro-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazol-5-one

(20): To a suspension of Raney Ni (100 mg) in MeOH (1 mL) was added cyano-ester compound 19 (40.0 mg) in 3 mL MeOH-DMF (1:3) and kept under the balloon pressure of ¾ gas for 24 h. After completion of the reaction (by TLC) cooled to room temperature, filtered through celite with the aid of EtOAc and the volatiles were removed under reduced pressure and the crude compound was purified by column chromatography (30-40% EtOAc + Hexane) to afford 20 as light brown solid. (26.0 mg, 72%); mp: > 300 °C; R/ = 0.3 (50% EtOAc + Hexane); ¾ NMR (500 MHz, DMSO) d 11.81 (s, 1H), 9.33 (d, 7 = 7.9 Hz, 1H), 8.55 (s, 1H), 8.07 (d, 7 = 7.7 Hz, 1H), 7.75 (d, 7 = 8.3 Hz, 1H), 7.66 (d, 7 = 8.1 Hz, 1H), 7.48 (t, 7 = 7.3 Hz, 1H), 7.44 - 7.39 (m, 1H), 7.33 (t, 7 = 7.4 Hz, 1H), 7.24-7.14 (m, 6H), 6.24 (s, 2H), 5.00 (s, 2H); ¹³C NMR (101 MHz, DMSO) d 172.7, 140.7, 140.5, 138.7, 133.5, 129.3, 129.0, 127.7, 127.1, 125.7, 125.2, 123.0, 122.7, 121.8, 120.9, 119.8, 119.5, 117.7, 114.9, 112.0, 111.0, 47.9, 45.8; IR (neat): D_max 765, 1332, 1450, 1658, 2505, 2954, 3221, 3327 cm ; HRMS (ESIMS) calcd. For C27H20N3O [M+H]⁺: calcd m/z 402.1606; found 402.1603.

Example 38: 6,7,12,13-Tetrahydro-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazol-5-one (3): To a solution of AlCb (66 mg, 0.5 mmol) in anisole (0.5 mL) at 0 °C was added a solution of compound 20 (20.0 mg, 0.05 mmol ) in anisole (0.5 mL), further the reaction mixture was heated at 110 °C for 1 h. After completion of the reaction (by TLC), it was cooled to room temperature, filtered through celite with the aid of EtOAc and the volatiles were removed under reduced pressure and the crude compound was purified by column chromatography (40-50% EtOAc + Hexane) to afford staurosporinone 3 as brownish-red solid (14.8 mg, 95%). R _f = 0.2 (50% EtOAc + Hexane); mp > 300

11.60 (s, 1H), 11.42 (s, 1H), 9.23 (d, 7 = 7.9 Hz, 1H), 8.48 (s, 1H), 8.05 (d, 7 = 7.7 Hz, 1H), 7.79 (d, 7 = 8.1 Hz, 1H), 7.72 (d, 7 = 8.1 Hz, 1H), 7.46 (dt, 7 = 19.7, 7.4 Hz, 2H), 7.31 (t, 7 = 7.4 Hz, 2H), 7.23 (t, 7 = 7.3 Hz, 1H), 4.97 (s, 2H); ¹³C NMR (101 MHz, DMSO-d6) S 172.4, 139.2, 139.0, 132.9, 127.9, 125.4, 125.2, 125.0 (2C), 122.8, 122.6, 121.1, 119.9, 118.9 (2C), 115.6, 114.1, 111.9, 111.3, 45.3; IR (neat): D_max 760, 1245, 1381, 1456, 1647, 1731, 2856, 2922 cm ¹; HRMS (ESIMS) calcd. For C20H14N3O [M+H]⁺: calcd m/z 312.1137; found 312.1135.

Preparation of indole-ynones of formula II (X=H):

Formula (IV) Formula (II)

R = Me, Bn, Ri = Me, Ph, 3-methyl phenyl, 4-ethyl phenyl, 4-OMe-phenyl, C1-C6 alkyl, cyclopropyl.

General Preparation of compound of formula IV

A solution of A , A- d i m c t h y l fo m a m i dc (90.0 mmol) in dichloromethane (50.0 mL) at 0 °C was slowly treated with POCI3 (75.0mmol) and stirred for 1 h. A solution of oxindole (30.0 mmol) in dichloromethane (30.0 mL) was added to the reaction mixture and the reaction stirred for 24 h at 25 °C. The reaction was quenched by pouring it into ice bath and adding NaHCCL until a pH of 7 was reached. The solution was allowed to warm to room temperature and was extracted with dichloromethane (3 x 50 mL). The combined organic layers were washed with saturated aq. NaHCCL, brine, and H2O. The organic phase was dried over Na₂S0₄, filtered, and concentrated in vacuo. The residue was purified by flash chromatography (1:4 EtO Ac/hexane) to afford 2-Chloro-Indole-3-carbaldehyde. The free NH was protected as methyl or benzyl using methyl iodide or benzyl bromide. To a stirred solution of 2-Chloro-Indole-3-carbaldehyde (5 mmol) in acetonitrile (20 mL) at 0 °C were added NaH (6 mmol) and stirred for 30 min. To this alkyl halide (6 mmol) was added and stirred at room temperature for 3 h. After completion of the reaction quenched by adding H2O (5 mL) drop wise further 15 mL of water is added, diluted with EtOAc (20 mL) and the layers were separated, the aqueous layer was extracted with EtOAc (3 x 20 mL). The combined organic layers were washed with saturated brine solution. The organic phase was dried over Na₂S0₄, filtered, and concentrated in vacuo. The residue was purified by flash chromatography (1:5 EtO Ac/hexane) to afford A-substitutcd 2-Chloro-Indole-3- carbaldehyde.

General procedure 2 for the preparation of ynones (4c to 4p) of formula II utilized for synthesis of representative carbazoles:

77-BuLi (1.1 mmol) was added to a stirring solution of alkyne (1.2 mmol) in anhydrous THF (5 mL) at -78 °C, and the resulting reaction mixture was stirred for another 15 min. at the same temperature. To this aldehyde (1 mmol) in THF (5 mL) was added drop wise and allowed to warm to room temperature and the reaction was monitored by TLC. After complete consumption of the starting material (monitored by TLC), the reaction mixture was quenched by drop wise addition of saturated aq. NH4CI (50 mL) solution and diluted with H2O (10 mL) and EtOAc (10 mL). The layers were separated and the aqueous layer was extracted with EtOAc (2 x 10 mL). The combined organic layer was washed with brine solution and dried over anhydrous Na2S04, concentrated under reduced pressure to afford the crude propargyl alcohol, which was used for oxidation directly. To a stirred solution of secondary alcohol (1 mmol) in DMSO (5 mL) at room temperature was added IBX (1.2 mmol) and the reaction mixture was stirred for 2 h. After complete consumption of the starting material (monitored by TLC), the reaction mixture was filtered through celite with the aid of EtOAc and the resulting filtrate was washed with cold H2O (10 mL x 2) and brine solution (10 mL) and the organic layer was dried over anhydrous Na₂S0₄. Volatiles were removed under reduced pressure and the obtained crude mixture was purified by silica gel column chromatography to yield the substituted ynones.

l-(l-Methylindol-3-yl)-3-phenylprop-2-yn-l-one (4a). To a two-neck round bottomed flask equipped with a stir bar was added phenyl acetylene (11.2 mmol, 1.14 g) and THE (7 mL). The stirred solution was cooled to 0 °C and flushed with argon. To this reaction mixture was added dropwise, n-BuLi (2.5 M in hexanes, 4.5 mL, 11.2 mmol) and the mixture was allowed to stir for 30 min at 0 °C. A- Methyl-3- indolecarboxaldehyde (9.3 mmol, 1.48 g) in THE (5 mL) was added dropwise and allowed to stir for 1 h at 0 °C. After completion, the reaction was quenched with saturated aq. NH₄CI solution and extracted with diethylether. The organic layers were combined, dried and concentrated under reduced pressure.

(oxidation with MnCL): The residue (alcohol) was dissolved in chloroform (10 mL) and MnCL (27.9 mmol, 2.43 g) was added to the solution. The suspension was refluxed for 1 h, the solution was cooled and filtered through a pad of celite, and the filtrate was concentrated. The residue was purified by column chromatography on silica gel to afford 1.24 g of the product.

Oxidation with IBX: To the solution of alcohol in DMSO (10 mL) was added IBX (11.2 mmol) and stirred at room temperature for 2 h. The mixture was quenched with water, extracted with diethyl ether and dried over anhydrous Na2S04, filtered and concentrated under reduced pressure as a pale yellow solid: mp 112-114 °C; ¹ H NMR (CDCL) d 3.81 (s, 3H), 7.29-7.43 (m, 6H), 7.61-7.64 (d, J = 7.2 Hz, 2H), 7.89 (s, 1H), 8.39-8.42 (m, 1H); ¹³C NMR 5 33.8, 87.8, 88.0, 110.1, 118.5, 120.9, 122.5, 123.2, 124.0, 125.9, 128.7, 130.2, 132.8, 137.9, 139.1, 171.3; IR (neat, cm-1) 3057, 1605.

l-(l-Allyl-lH-indol-3-yl)-3-phenylprop-2-yn-l-one (4c): By following the general procedure 2 using l-allyl-lH-indole-3-carbaldehyde and phenylacetylene, ynone 4c was prepared as light brown solid (205 mg, 72%).

l-(l-Methyl-lH-indol-3-yl)-3-(m-tolyl)prop-2-yn-l-one (4d): By following the general procedure 2 using 1 -methyl- lH-indole-3-carbaldehyde and 3-methyl phenylacetylene, ynone 4d was prepared as brown viscous oil (221 mg, 81%).

3-(4-Ethylphenyl)-l-(l-methyl-lH-indol-3-yl)prop-2-yn-l-one (4e): By following the general procedure 2 using 1 -methyl- lH-indole-3-carbaldehyde and 4-ethyl phenylacetylene, ynone 4e was prepared as light brown solid (215 mg, 75%).

3-(4-Methoxyphenyl)-l-(l-methyl-lH-indol-3-yl)prop-2-yn-l-one (4f): By following the general procedure 2 using l-methyl-lH-indole-3-carbaldehyde and 4-methoxy phenylacetylene, ynone 4f was prepared as light brown solid (217 mg, 75%).

l-(l-Methyl-lH-indol-3-yl)hept-2-yn-l-one (4g): By following the general procedure 2 using l-methyl-lH-indole-3-carbaldehyde and 1-hexyne, ynone 4g was prepared as pale yellowish oil (181.5 mg, 76%).

3-Cyclopropyl-l-(l-methyl-lH-indol-3-yl)prop-2-yn-l-one (4h): By following the general procedure 2 using 1 -methyl- lH-indole-3-carbaldehyde and cyclopropyl acetylene, ynone 4h was prepared as light brown solid (176.2 mg, 79%).

l-(5-Methoxy-l-methyl-lH-indol-3-yl)-3-phenylprop-2-yn-l-one (4i): By following the general procedure 2 using 5-methoxy- 1-methyl- lH-indole-3-carbaldehyde and phenylacetylene, ynone 4i was prepared as dark brown solid (222 mg, 77%).

l-(l-Benzyl-lH-indol-3-yl)but-2-yn-l-one (4j): To a solution of 1-benzyl indole-3- carbaldehyde (235 mg, 1 mmol) in THF (3 mL) at -20 °C was added 1-propynyl magnesium bromide (2.2 mL, 1.1 mmol, 0.5 M in THF) drop wise and stirred for 1 h. After complete consumption of the starting material (monitored by TLC), the reaction mixture was quenched by drop wise addition of saturated aq. NH4CI (10 mL) solution and diluted with H2O (30 mL) and EtOAc (20 mL). The layers were separated and the aqueous layer was extracted with EtOAc (3 x 20 mL). The combined organic layer was washed with brine solution and dried over anhydrous NaiSCL, concentrated under reduced pressure to afford the crude alcohol, which was directly used for next reaction. To a stirred solution of secondary alcohol (275 mg, 1 mmol) in DMSO (5 mL) at room temperature was added IBX (336 mg, 1.2 mmol) and the reaction mixture was stirred for 2 h. After complete consumption of the starting material (monitored by TLC), the reaction mixture was filtered through celite with the aid of EtOAc and the resulting filtrate was washed with cold H2O (10 mL x 2) and brine solution (10 mL) and the organic layer was dried over anhydrous Na₂S0₄. Volatiles were removed under reduced pressure and the obtained crude mixture was purified by silica gel column chromatography to yield the substituted ynone (4j) prepared as pale yellowish oil (240 mg,

88%).

3-(2-Fluorophenyl)-l-(l-methyl-lH-indol-3-yl)prop-2-yn-l-one (4k): By following the general procedure 2 using 1 -methyl- lH-indole-3-carbaldehyde and 2-fluoro phenylacetylene, ynone 4k was prepared as dark brown solid (202 mg, 73%).

Preparation of chloro-substituted indole -ynones of formula II (X=C1):

Formula IV Formula II

Ri=Me, Bn; and R2=Phenyl, 4-fluorophenyl, 4-nbutyl phenyl, n-butyl, C1-C6 alkyl, or cyclopropyl

The chlorosubstituted indole-ynones were synthesized starting from commercially available oxindoles as shown in scheme below. Accordingly, the oxindole was treated with DMF and POCI3 following the procedure known in the prior art to furnish 2-chloro-indole-3- carbaxaldehyde which was further treated with NaH and alkyl halide to get the A-substitutcd chloro indole derivative of formula IV. This compound of formula IV was later treated with acetylene compounds in presence of n-Buli to get the secondary alcohol followed by oxidation with IBX (Chem. Eur. J. 2016, 22, 12655) or MnC (Org. Lett. 2005, 7, 5203) to furnish the chloro-substituted indole-ynone of formula II following the process known in the prior art.

l-(l-Benzyl-2-chloro-lH-indol-3-yl)-3-phenylprop-2-yn-l-one (41): By following the general procedure 2 using l-benzyl-2-chloro indole-3-carbaldehyde and phenylacetylene, ynone 41 was prepared as brownish yellow solid (277 mg, 75%).

l-(2-Chloro- 1-methyl- lH-indol-3-yl)-3-(4-fluorophenyl)prop-2-yn-l-one (4m): By following the general procedure 2 using l-methyl-2-chloro indole-3 -carbaldehyde and 4-fluoro phenylacetylene, ynone 4m was prepared as light brown solid (221 mg, 71%).

3-(4-butylphenyl)-l-(2-chloro-l-methyl-lH-indol-3-yl)prop-2-yn-l-one (4n): By following the general procedure 2 using l-methyl-2-chloro indole-3 -carbaldehyde and 4-n-butyl phenylacetylene, ynone 4n was prepared as dark brown oil (238 mg, 68%). l-(2-Chloro- 1-methyl- lH-indol-3-yl)hept-2-yn-l-one (4o): By following the general procedure 2 using l-methyl-2-chloro indole-3-carbaldehyde and 1-hexyne 4o was prepared as pale yellowish oil (202 mg, 74%).

l-(2-Chloro- 1-methyl- lH-indol-3-yl)-3-phenylprop-2-yn-l-one (4p): By following the general procedure 2 using 1 -methyl-2 -chloro indole-3-carbaldehyde and phenylacetylene, ynone 4p was prepared as light orange solid (211 mg, 72%).

SIGNIFICANCE OF THE WORK CARRIED OUT

In view of the importance of carbazoles a new and efficient process for the preparation of carbazoles from indole-ynones and nitromethanes is presented. The indole-ynones can be easily accessible readily available commercial materials in a two-step process. The present process method synthesis of substituted carbazoles of formula I by us serves as a highly effective new method for the synthesis of several carbazoles and process for synthesis of three natural products carbazomycin A (1), calothrixin B (2) and staurosporinone (3) respectively thereof.

ADVANTAGES OF THE INVENTION

The various advantages of the present process are given below

• The main advantage of the present invention is that it provides an efficient process for the preparation of substituted carbazoles from indole-ynones via benzannulation reaction.

• The main advantage of the present invention is that it provides an efficient process for the preparation of nitro substituted carbazoles avoiding difficult nitration reaction on the carbazole moiety.

• Another advantage of the present invention is the employment of easily available raw materials, nitro alkanes, phenyl acetylenes, for accessing indole-ynone substrates.

• The duration of the Cadogan cyclization has been reduced enormously utilizing monowave synthesizer.

• Further advantage of the invention is employment of mild base CS₂CO₃.

• Another advantage of this process involves utility of carbazoles synthesized by the developed process for the three natural product synthesis. That is 4- step synthesis for carbazomycin A, 6- step synthesis for calothrixin B and 5- step synthesis sequence for staurosporinone from the carbazoles synthesized herein.

Claims

WE CLAIM

1. A compound of general formula (I),

wherein‘Ri’ is H, C1-C6 alkyl, benzyl, or allyl; R2 is H, C1-C6 alkyl, cyclopropyl, phenyl, aryl, heteroaryl, C1-C6 methoxy carbonyl, or NO2; R3 is H, C1-C6 alkyl, cyclopropyl, phenyl aryl, heteroaryl, 4-methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, 2-Fluoro phenyl, 4- Fluoro phenyl, or 4-butyl phenyl; R4 is H, benzoyl, -CC Et, -CHO, Br, or -OMe; R5 is OH, OMOM, OMe, CN, or OTf; R₆ is H, or O-alkyl; and R3-R4 is -CHNCH2CH2.

2. The compound of general formula (I) as claimed in claims 1 is selected from the group consisting of:

9-Methyl-2-phenyl-9H-carbazol-4-ol (6a);

9-Benzyl-2-phenyl-9H-carbazol-4-ol (6b);

9-Allyl-2-phenyl-9H-carbazol-4-ol (6c);

9-Methyl-2-(m-tolyl)-9H-carbazol-4-ol (6d);

2-(4-Ethylphenyl)-9-methyl-9H-carbazol-4-ol (6e);

2-(4-Methoxyphenyl)-9-methyl-9H-carbazol-4-ol (6f);

2-Butyl-9-methyl-9H-carbazol-4-ol (6g);

2-Cyclopropyl-9-methyl-9H-carbazol-4-ol (6h);

6-Methoxy-9-methyl-2-phenyl-9H-carbazol-4-ol (6i);

l,9-Dimethyl-2-phenyl-9H-carbazol-4-ol (6j);

l-Ethyl-9-methyl-2-phenyl-9H-carbazol-4-ol (6k);

Methyl 3-(4-hydroxy-9-methyl-2-phenyl-9H-carbazol-l-yl)propanoate (61);

9-Benzyl- l,2-dimethyl-9H-carbazol-4-ol (6m);

Ethyl 4-hydroxy-9-methyl-2-phenyl-9H-carbazole-3-carboxylate (7a);

Ethyl 2-cyclopropyl-4-hydroxy-9-methyl-9H-carbazole-3-carboxylate (7b);

(2-(2-fluorophenyl)-4-hydroxy-9-methyl-9H-carbazol-3-yl)(phenyl)methanone (7e);

(4-Hydroxy-6-methoxy-9-methyl-2-phenyl-9H-carbazol-3-yl)(phenyl)methanone

(7f);

9-Benzyl- l-nitro-2-phenyl-9H-carbazol-4-ol (8a);

- 2-(4-Fluorophenyl)-9-methyl-l-nitro-9H-carbazol-4-ol (8b);

2-(4-Butylphenyl)-9-methyl-l-nitro-9H-carbazol-4-ol (8c);

2-Butyl-9-methyl-l-nitro-9H-carbazol-4-ol (8d);

Ethyl 9-benzyl-4-hydroxy-l-nitro-2-phenyl-9H-carbazole-3-carboxylate (8e); Ethyl 2-(4-fluorophenyl)-4-hydroxy-9-methyl-l-nitro-9H-carbazole-3-carboxylate (8f);

(4-Hydroxy-9-methyl-l-nitro-2-phenyl-9H-carbazol-3-yl)(phenyl)methanone

(8g);

- (2-Cyclopropyl-4-hydroxy-9-methyl-l-nitro-9H-carbazol-3-yl)(phenyl)methanone

(8i)

3. A process for the preparation of carbazoles of general formula (I) comprising:

Formula il

- reacting indole-ynone of formula (II) , with nitroalkane or substituted nitroalkane of formula (III)

Formula I wherein‘Ri’ is H, C1-C6 alkyl, benzyl, or allyl; R3 is H, C1-C6 alkyl, cyclopropyl, phenyl aryl, heteroaryl, 4-methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, or 2-Fluoro phenyl; R₆ is H, or O-alkyl; R3-R4 is -CHNCH2CH2-; and‘X’ is H, F, Cl, I, or Br.

4. The process as claimed in claims 3, wherein base is selected from the group consisting of K2CO3, CS2CO3 or Na₂C0_3.

5. The process as claimed in claims 3, wherein the solvent is selected from the group consisting of DMF, DMSO or Dioxane.

6. A compound of general formula (II):

wherein‘Ri’ is H, C1-C6 alkyl, benzyl, or allyl; R3 is H, C1-C6 alkyl, benzyl, substituted benzyl, cyclopropyl, phenyl aryl, heteroaryl, 4-methoxy phenyl, 4-ethyl phenyl, 2-methyl phenyl, or 2-Fluoro phenyl; R₆ is H, or O-alkyl; R3-R4 is -CHNCH2CH2-; and‘X’ is H, F, Cl, I, or Br.

7. The compound of general formula (II) as claimed in claims 6 is selected from the group consisting of:

8. A process for the preparation of carbazomycin A of Formula (1) comprising:

1 1

a) O-methylation of compound of Formula (6m) to corresponding methoxy ether of Formula

(9);

b) bromination of compound of Formula (9) to compound of Formula (10);

c) converting compound of Formula (10) to dimethoxy compound of Formula (11); and d) V-dcbcnzylation of compound of Formula (11) to carbazomycin A of Formula (1).

9. A process for the preparation of calothrixin B of Formula (2) comprising:

a) protecting compound of Formula (8a) to obtain compound of Formula (12); b) Cadogan cyclization of compound of Formula (12) to indolocarbazole compound of Formula (13);

c) Vilsmayer Haack formylation of compound of Formula (13) to aldehyde of Formula (14); d) protecting compound of Formula (14) to obtain compound of Formula (15);

f) N-debenzylation of compound of Formula (16) to calothrixin B of Formula (2).

10. A process for the preparation of staurosporinone of Formula (3) comprising:

a) Benzoannulation of chlorosubstituted /V-benzylated indole-ynone of Formula (41);

b) converting compound of Formula (8e) to triflate compound of Formula (17);

c) cyanation of compound of Formula (17) to compound of Formula (18);

d) Cadogen cyclization of compound of Formula (18) to compound of Formula (19);

e) converting compound of Formula (19) to /V-benzylated staurosporinone of Formula (20); and

f) debenzylation of compound of Formula (20) to staurosporinone of Formula (3).