WO2023158769A1 - Processes for the preparation of n-(1- methylcyclopropyl)-2-(3 -pyridinyl)-2h- indazole-4-carboxamide and intermediates thereof - Google Patents

Processes for the preparation of n-(1- methylcyclopropyl)-2-(3 -pyridinyl)-2h- indazole-4-carboxamide and intermediates thereof Download PDF

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WO2023158769A1
WO2023158769A1 PCT/US2023/013266 US2023013266W WO2023158769A1 WO 2023158769 A1 WO2023158769 A1 WO 2023158769A1 US 2023013266 W US2023013266 W US 2023013266W WO 2023158769 A1 WO2023158769 A1 WO 2023158769A1
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compound
solvent system
reaction
aspects
base
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English (en)
French (fr)
Inventor
Ahmad EL-AWA
Linli He
Raju Mahadevrao KHARATKAR
Jianhua Mao
Jigarkumar MISTRY
Mahesh Patil
Christina S. Stauffer
Pankajkumar VEKARIYA
James Anderson Wright
Ty Wagerle
David Alan Clark
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FMC Corp
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FMC Corp
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Priority to JP2024548366A priority Critical patent/JP2025507562A/ja
Priority to MX2024010028A priority patent/MX2024010028A/es
Priority to IL314647A priority patent/IL314647A/en
Priority to EP23711266.9A priority patent/EP4479393A1/en
Priority to US18/839,255 priority patent/US20250163010A1/en
Priority to KR1020247030594A priority patent/KR20240152344A/ko
Priority to AU2023222774A priority patent/AU2023222774A1/en
Priority to CN202380022266.3A priority patent/CN118715213A/zh
Publication of WO2023158769A1 publication Critical patent/WO2023158769A1/en
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    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
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    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
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    • B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
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    • C07C209/28—Preparation of compounds containing amino groups bound to a carbon skeleton by reductive alkylation of ammonia, amines or compounds having groups reducible to amino groups, with carbonyl compounds by reduction with other reducing agents
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    • C07C209/46—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers by reduction of carboxylic acids or esters thereof in presence of ammonia or amines
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    • C07C209/44—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers
    • C07C209/50—Preparation of compounds containing amino groups bound to a carbon skeleton by reduction of carboxylic acids or esters thereof in presence of ammonia or amines, or by reduction of nitriles, carboxylic acid amides, imines or imino-ethers by reduction of carboxylic acid amides
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    • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
    • C07C211/33—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C211/34—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of a saturated carbon skeleton
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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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    • C07C233/57—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C233/58—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of rings other than six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
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    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/09—Preparation of carboxylic acids or their salts, halides or anhydrides from carboxylic acid esters or lactones
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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
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    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/18—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/20—Oxygen atoms
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    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/60—Reduction reactions, e.g. hydrogenation
    • B01J2231/64—Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
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    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
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    • C07C2601/02—Systems containing only non-condensed rings with a three-membered ring

Definitions

  • the process comprising forming a reaction mixture comprising compound 223, CH3Cl, an alkali metal iodide, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 775 according to the following scheme .
  • Another aspect of the disclosure is directed to a process for the preparation of compound 200 according to a first scheme, a second scheme, or a third scheme.
  • the first such scheme for preparing compound 200 comprises steps 1 to 3.
  • Step 1 comprises forming a reaction mixture comprising compound 775, HCl, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 069 according to the following reaction scheme .
  • Step 2 comprises forming a reaction mixture comprising compound 069, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 079 according to the following reaction scheme
  • Step 3 comprises forming a reaction mixture comprising compound 079, an oxidizing agent, optionally a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 200 according to the following reaction scheme .
  • the second such scheme for preparing compound 200 comprises steps 1 to 2.
  • Step 1 comprises forming a reaction mixture comprising compound 900, CHX 3 , a base, a solvent system, and a phase transfer catalyst, and reacting the reaction mixture to form a reaction product mixture comprising compound 905 according to the following reaction scheme wherein R is selected from COOCH 3 , COOCH 2 CH 3 , COOH, and CN, and wherein each X is independently selected from Cl, Br, and I.
  • Step 1b forming a reaction mixture comprising compound 905, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 906 according to the following reaction scheme
  • Step 2 comprises forming a reaction mixture comprising compound 906, a reducing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 200 according to the following reaction scheme
  • R is COOH
  • the process comprises Step 2’, Step 2’ comprising forming a reaction mixture comprising compound 905, a reducing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 200 according to the following scheme [15]
  • the third such scheme for preparing compound 200 comprises steps 1 and 2.
  • Step 1 comprises forming a reaction mixture comprising acetic acid, compound 100, a base, a photocatalyst, and a solvent system, and reacting the reaction mixture by exposure to light emitted from at least one light source to form a reaction product mixture comprising compound 110 according to the following reaction scheme .
  • Step 2 comprises forming a reaction mixture comprising compound 110, a solvent system, and a base, and reacting the reaction mixture to form a reaction product mixture comprising compound 200 according to the following reaction scheme . .
  • Another aspect of the disclosure is directed to a process for preparing compound 070, the process comprising a first scheme and a second scheme.
  • Step 1 comprising substep (a) comprising forming a reaction mixture comprising compound 200, a chlorinating reagent, optionally a catalyst, and a solvent system and reacting the reaction mixture to form a reaction product mixture comprising an acid chloride intermediate, followed by substep (b) comprising forming a reaction mixture by combining the reaction product mixture from substep (a) with an ammonia source and reacting the reaction mixture to form a reaction product mixture comprising compound 144 according to the following reaction scheme .
  • Step 2 comprises substep (a) comprising forming a reaction mixture comprising compound 144, a base, an oxidant, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising a N- halocarboxamide intermediate, followed by substep (b) comprising heating the reaction product mixture comprising the N-halocarboxamide intermediate to form a reaction product mixture comprising compound 070 according to the following reaction scheme [22]
  • the second scheme comprising three steps: [23] Step 1 comprising forming a reaction mixture comprising compound 900, CHX 3 , a base, a solvent system, and a phase transfer catalyst, and reacting the mixture to form a reaction product mixture comprising compound 905 according to the following reaction scheme wherein R is CONH2; and wherein each X is independently selected from Cl, Br, and I; and [24] Step 2 comprising forming a reaction mixture comprising compound 905, a reducing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising
  • compound 905a an intermediate compound useful for preparation of compound 070 and having the following structure: [27]
  • Another aspect of the disclosure is directed to a process for the preparation of compound 070, the process comprising a first, a second and a third scheme, the first scheme comprising: [28] Step 1 comprising forming a reaction mixture comprising compound 403, an acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 070 according to the following scheme ; the second scheme comprising two steps, comprising: [29] Step 1 comprising forming a reaction mixture comprising compound 994, an activator, and a solvent system, reacting the reaction mixture to form a reaction product mixture comprising compound 403 according to the following scheme .
  • Step 2 comprising forming a reaction mixture comprising compound 403, and acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 070 according to the following scheme .
  • the third scheme comprising three steps, comprising: [32] Step 1 comprising forming a reaction mixture comprising compound 079, a source of hydroxylamine, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 994 according to the following reaction scheme .
  • Step 2 comprising forming a reaction mixture comprising compound 994, an activator, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 403 according to the following reaction scheme
  • Step 3 comprising forming a reaction mixture comprising compound 403, an acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 070 according to the following reaction scheme .
  • Another aspect of the disclosure is directed to a process for the preparation of compound 070. The process comprises forming a reaction mixture comprising acetonitrile, ethyl magnesium halide, a titanium reagent, and a solvent, reacting the reaction mixture, adding an acid to the reaction mixture, and further reacting the reaction mixture to form a reaction product mixture comprising compound 070 according to the following scheme
  • Another aspect of the disclosure is directed to a process for the preparation of compound 093a, the process comprising steps 1 to 4.
  • Step 1 comprises forming a reaction mixture comprising compound 3 solvent system, and reacting the reaction mixture under photochemical conditions to form a reaction product mixture comprising compound 181a, according to the following reaction scheme .
  • Step 2 comprises forming compound 378 by the (i) the combination of steps 2(a) and 2(b) or by (ii) step 2.
  • Step 2(a) comprises forming a reaction mixture comprising compound 181a, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 050 according to the following reaction scheme .
  • Step 2(b) comprises forming a reaction mixture comprising compound 050, an oxidizing reagent, a phase transfer catalyst, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 378 according to the following reaction scheme
  • Step 2 comprises forming a reaction mixture comprising compound 181a, an oxidizing reagent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 378 according to the following reaction scheme .
  • Step 3 comprises forming a reaction mixture comprising compound 378, 3-aminopyridine, an acid catalyst, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 003a according to the following reaction scheme .
  • Step 4 comprises forming a reaction mixture comprising compound 003a, a phosphine or a phosphite, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 093a according to the following reaction scheme 003a 093a .
  • the phosphine is selected from tri(C 1 -4 ) alkyl phosphine and triaryl phosphine and the phosphite is selected from tri(C 1 -4 ) alkyl phosphite and triaryl phosphite.
  • Another aspect of the disclosure is directed to a process for the preparation of compound 093a, the process comprising steps 1 to 7.
  • Step 1 comprises forming a reaction mixture comprising compound 150, an acid, 3-aminopyridine, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 086 according to the following reaction scheme .
  • Step 2 comprises forming a reaction mixture comprising compound 086, a reducing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 084 according to the following reaction scheme .
  • Step 3 comprises forming a reaction mixture comprising compound 084, a reagent for converting an amine moiety to a nitrosamine moiety, an acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 085 according to the following reaction scheme [48]
  • Step 4 comprises (a) forming a reaction mixture comprising compound 085, a reductant, a base, and a solvent system, and reacting the reaction mixture followed by (a) acidification to form a reaction product mixture comprising compound 048 according to the following reaction scheme [49]
  • Step 5 comprises forming a reaction mixture comprising compound 048, acetic anhydride, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 083 according to the following reaction scheme [50]
  • Step 6 comprises forming a reaction mixture comprising compound 083, a ligand, a transition metal catalyst, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising
  • Step 7 comprises forming a reaction mixture comprising compound 082, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 093a according to the following reaction scheme 093a
  • Another aspect of the disclosure is directed to a process for the preparation of compound 093a, the process comprising steps 1-3.
  • Step 1 comprises forming a reaction mixture solution comprising compound 150, acetohydrazine, a solvent system, and an organic acid, and reacting the reaction mixture to form a reaction product mixture comprising compound 197 according to the following reaction scheme p 1 197 .
  • Step 2 comprises forming a reaction mixture comprising compound 197, a reducing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 040 according to the following reaction scheme 1 Step 2 040 .
  • Step 3 comprises forming a reaction mixture comprising compound 040, 3-bromopyridine, a ligand, a transition metal catalyst, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 093a according to the following reaction scheme
  • Step 1 comprises forming a reaction mixture comprising compounds 181a or 181b, compound 520, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compounds 182a or 182b, respectively, according to the following reaction scheme.
  • Step 2 comprises forming a reaction mixture comprising compounds 182a or 182b, a reductant, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compounds 093a or 093b, respectively, according to the following reaction scheme [61]
  • the second such scheme for preparing compounds 093a or 093b comprises steps 1 to 3.
  • Step 1 comprises forming a reaction mixture comprising compounds 114a or 114b, an oxidizing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compounds 115a or 115b, respectively, according to the following reaction scheme.
  • Step 2 comprises forming a reaction mixture comprising compounds 115a or 115b, a source of bromine or a source of chlorine, and a solvent system and reacting the reaction mixture under photochemical conditions to form a reaction product mixture comprising compound 116a, 116b, 116c, or 116d, according to the following reaction scheme.
  • Step 3 comprises forming a reaction mixture comprising compound116a, 116b, 116c, or 116d, compound 520, and a solvent system and reacting the reaction mixture to form a reaction product mixture comprising compound 093a, or 93b, respectively, according to the following reaction scheme.
  • Another aspect of the disclosure is directed to an alternate process to prepare compound 182a or 182b.
  • the process comprises forming a reaction mixture comprising compound 003a or 003b, a reducing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 182a or 182b, respectively, according to the following reaction scheme.
  • Another aspect of the disclosure is directed to a process for the preparation of compound 061.
  • the process comprises forming a reaction mixture comprising compound 093a or 093b, CO, a catalyst, a ligand, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 061 according to the following reaction scheme
  • Step 1 comprises forming a reaction mixture comprising compound 400, an oxidizing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 500 according to the following reaction scheme
  • Step 2 comprises forming a reaction mixture comprising compound 500, a source of bromine or a source of chlorine, and a solvent system, and reacting the reaction mixture under photochemical conditions to form a reaction product mixture comprising compound 510a or 510b, according to the following reaction scheme
  • Step 3 comprises forming a reaction mixture comprising compound 510a or 510b, compound 520, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 038 according to the following reaction scheme 5 0b .
  • the second such scheme for preparing compound 038 comprises steps 1 to 3.
  • Step 1 comprises forming a reaction mixture comprising compound 400, a source of bromine or a source of chlorine, and a solvent system, and reacting the reaction mixture by exposure to a source of light to form a reaction product mixture comprising compound 410 according to the following reaction scheme .
  • Step 2 comprising forming a reaction mixture comprising compound 410, compound 420, an acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 430 according to the following reaction scheme .
  • Step 3 comprises forming a reaction mixture comprising compound 430, a strong acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 038 according to the following reaction scheme .
  • the third such scheme for preparing compound 038 comprises forming a reaction mixture comprising compound 093a or 093b, a catalyst, a ligand, CO, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 038 according to the following reaction scheme
  • Another aspect of the disclosure is directed to a process for the preparation of compound 061, the process comprising forming a reaction mixture comprising compound 038, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 061 according to the following reaction scheme [78]
  • Another aspect of the disclosure is directed to a process for preparing compound 038, the process comprising forming a reaction mixture comprising compound 061, an acid, optionally an additive, and a solvent system containing methanol, and reacting the reaction mixture to form a reaction product mixture comprising compound 038 according to the following reaction scheme [79]
  • an intermediate compound useful for preparation of compound 093a and having the following structure are examples of compounds useful for preparation of compound 093a and having the following structure.
  • an intermediate compound useful for preparation of compound 093a and having the following structure and the hydrochloride salt [83] In one aspect, an intermediate compound useful for preparation of compound 093a and having the following structure: [84] In one aspect, an intermediate compound useful for preparation of compound 093a and having the following structure: [85] In one aspect, an intermediate compound useful for preparation of compound 093a and having the following structure . [86] In one aspect, a compound having the structure of compound 520a: . [87] In one aspect, a compound having the structure of compounds 182a or 182b . [88] In one aspect, a compound having the structure of compound 115b:
  • a compound having the structure of compound 116a-d [90] In one aspect, a compound having the structure of compound 500:
  • a compound having the structure of compound 510a or 510b [92] Another aspect of the disclosure is directed to a process for preparing compound 092, the process comprising steps 1 and 2.
  • Step 1 comprises forming a reaction mixture comprising compound 061, a chlorinating reagent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 930 according to the following reaction scheme .
  • Step 2 comprises forming a reaction mixture comprising compound 930, compound 070, an organic base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 092 according to the following reaction scheme .
  • Another aspect of the disclosure is directed to a process for preparing compound 092, the process comprising forming a reaction mixture comprising compound 093a or 93b, compound 070, a catalyst, a ligand, CO, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 092 according to the following reaction scheme.
  • Another aspect of the disclosure is directed to a process for preparing compound 092, the process comprising forming a reaction mixture comprising compound 061, compound 070, an activator, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 092 according to the following reaction scheme
  • Another aspect of the disclosure is directed to a process for preparing compound 092, the process comprising forming a reaction mixture comprising compound 038, compound 070, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 092 according to the following reaction scheme [98]
  • Another aspect of the disclosure is directed to a process for preparing a compound 092 salt, the process comprising forming a reaction mixture comprising compound 092, a solvent system, an acid, and reacting the reaction mixture to form a reaction product mixture comprising compound 092 salt according to the following reaction scheme .
  • Another aspect of the disclosure is directed to a polymorph of N-(1- methylcyclopropyl)-2-(3-pyridinyl)-2H-indazole 4-carboxamide designated Form A characterized by a X-ray powder diffraction pattern in accordance with FIG.1.
  • Another aspect of the disclosure is directed to a polymorph of N-(1- methylcyclopropyl)-2-(3-pyridinyl)-2H-indazole 4-carboxamide designated Form B characterized by a X-ray powder diffraction pattern in accordance with FIG.2.
  • FIG.1 shows an XRPD pattern for N-(1-methylcyclopropyl)-2-(3- pyridinyl)-2H-indazole 4-carboxamide Form A prepared according to the examples of the present disclosure.
  • FIG.2 shows an XRPD pattern for N-(1-methylcyclopropyl)-2-(3- pyridinyl)-2H-indazole 4-carboxamide Form B prepared according to the examples of the present disclosure.
  • the disclose is generally directed to improved processes for the preparation of N-(1-methylcyclopropyl)-2-(3-pyridinyl)-2H-indazole 4-carboxamide, designated as compound 092 herein and of the structure , and intermediates thereof.
  • inorganic base generally includes sodium, potassium, ammonium, calcium, magnesium, iron, zinc, copper, manganese, and aluminum salts.
  • Non-limiting examples include phosphates such as dipotassium monohydrogen phosphate, potassium dihydrogen phosphate, tripotassium phosphate, disodium monohydrogen phosphate, sodium dihydrogen phosphate, trisodium phosphate, diammonium monohydrogen phosphate, ammonium dihydrogen phosphate and triammonium phosphate; acetates such as potassium acetate, sodium acetate and ammonium acetate; formates such as potassium formate and sodium formate; carbonates such as cesium carbonate, potassium carbonate, sodium carbonate, potassium hydrogen carbonate, and sodium hydrogen carbonate; ammonium hydroxide; and alkali metal hydroxides such as lithium hydroxide, sodium hydroxide and potassium hydroxide.
  • phosphates such as dipotassium monohydrogen phosphate, potassium dihydrogen phosphate, tripotassium phosphate, disodium monohydrogen phosphate, sodium dihydrogen phosphate, trisodium phosphate, diammoni
  • the inorganic bases may be used singly, or in combination of two or more kinds thereof.
  • the term “organic base” generally includes primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, such as pyridine, isopropylamine, trimethylamine, diethylamine, triethylamine, triethanolamine, diisopropylamine, ethanolamine, 2-diethylaminoethanol, trimethylamine, dicyclohexylamine, lysine, arginine, histidine, caffeine, procaine, hydrabamine, choline, betaine, ethylenediamine, glucosamine, methylglucamine, theobromine, purines, piperazine, piperidine, N-ethylpiperidine, and polyamine resins.
  • organometallic base generally includes organolithium, organomagnesium, organoaluminum, or organozinc compounds.
  • organolithiums such as methyl lithium, n-butyl lithium, sec-butyl lithium, tert-butyl lithium
  • organomagnesiums such as methyl magnesium chloride, methyl magnesium bromide, methyl magnesium iodide, ethyl magnesium chloride, ethyl magnesium bromide iso-propyl magnesium chloride, iso- propyl magnesium bromide
  • organoaluminums such as trimethyl aluminum, triethylaluminum, triisobutylaluminum.
  • inorganic acid refers to an acid comprising an inorganic component.
  • inorganic acids include mineral acids including, but not limited to hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, nitric acid, phosphoric acid, and boric acid.
  • the inorganic acid may be used alone, or in combination of two or more kinds thereof.
  • organic acid refers to an organic compound that acts an acid. Examples of organic acids include but are not limited carboxylic acids.
  • organic acids include, but are not limited to, formic acid, oxalic acid, malonic acid, succinic acid, glutaric acid, butanedioic acid, adipic acid, tartaric acid and citric acid.
  • the organic acid may be used alone, or in combination of two or more kinds thereof.
  • non-polar solvent refers to a solvent without significant partial charges on any atoms or a solvent where polar bonds are arranged in such a way that the effect of their partial charges cancel out.
  • Non- limiting examples of non-polar solvents include pentane, hexane, heptane, cyclopentane, cyclohexane, benzene, toluene, xylenes, 1,4-dioxane, dichloromethane (“DCM”), methyl tert-butyl ether (“MTBE”), chloroform, carbon tetrachloride, diethyl ether, and combinations thereof.
  • DCM dichloromethane
  • MTBE methyl tert-butyl ether
  • chloroform carbon tetrachloride
  • diethyl ether diethyl ether
  • Non-limiting examples of polar aprotic solvents include tetrahydrofuran (“THF”), methyl tetrahydrofuran (“Me-THF”), ethyl acetate (“EA”), acetone, dimethylformamide (“DMF”), dimethylacetamide (“DMAc”), acetonitrile (“ACN”), cyclopentylmethyl ether (“CPME”), petroleum ether, N-methyl-2-pyrrolidone (“NMP”), trifluorotoluene, chlorobenzene, anisole, and dimethyl sulfoxide (“DMSO”).
  • the aprotic solvent is a low molecular weight ester.
  • Non-limiting examples of aprotic low molecular weight ester solvents include methyl acetate, ethyl acetate, n-propyl acetate, i-propyl acetate, i-butyl acetate, propylene glycol methyl ether acetate, monoethyl ether acetate, and combinations thereof.
  • the term “polar protic solvent” refers to a solvent having a labile hydrogen bound to an oxygen atom or a nitrogen atom.
  • Non-limiting examples of polar protic solvents include formic acid, n-butanol, i-propanol, n- propanol, ethanol, methanol, acetic acid, water, and combinations thereof.
  • solvent refers to a non-polar solvent, an aprotic solvent, a polar protic solvent, and combinations thereof.
  • solvent system refers to a solvent or mixture of solvents. Solvent systems may comprise, or predominantly comprise, the indicated solvent or combination of solvents. Solvent systems may further comprise residual solvent from one or more preceding process steps.
  • reducing agent refers to a compound that donates electrons, either directly or through a hydride (“H-)”.
  • Non-limiting examples of reducing agents include sodium, potassium, zinc, iron, magnesium, sodium borohydride, potassium borohydride, p-toluenesulfonic acid, sodium bis(2- methoxyethoxy)aluminum hydride, sodium bisulfite, sodium hydrogensulfite, sodium hydrosulfite, sodium tetrahydroborate, potassium tetrahydroborate, sodium triacetoxyborohydride, trichlorosilane, triphenylphosphite, triethylsilane, trimethylphosphine, triphenylphosphine, diborane, diethoxymethylsilane, diisobutylaluminum hydride, diisopropylaminoborane, lithium aluminum hydride, and lithium triethylborohydride.
  • oxidizing agent refers to a compound that receives an electron.
  • oxidizing agents include: hypochlorite, chlorate, and perchlorate; peroxides such as H 2 O 2 ; O 2 ; O 3 ; N 2 O; halogens such as F 2 , Cl 2 , Br 2 , and I 2 ; HNO 3 ; KNO 3 ; H 2 SO 4 ; H 2 S 2 O 8 ; and H 2 SO 5 .
  • alkyl refers to a saturated linear or branched chain monovalent hydrocarbon group.
  • the alkyl group is suitably one to six carbon atoms (C 1-6 ), one to four carbon atoms (C 1-4 ), or one to three carbon atoms (C 1-3 ).
  • Non-limiting examples of alkyl groups include methyl (Me, -CH 3 ), ethyl (Et, -CH 2 CH 3 ), 1-propyl (n-Pr, -CH 2 CH 2 CH 3 ), 2-propyl (i-Pr, -CH(CH 3 ) 2 ), 1-butyl (n-Bu, -(CH 2 ) 3 CH 3 ), and 1,1-dimethylethyl (t-buyl, (CH 3 ) 3 C-).
  • the term “source of light” refers to visible light such as supplied by sunlight or a light source such as a xenon lamp, a halogen lamp, a fluorescent lamp, a diode or a mercury lamp.
  • a filter that cuts wavelengths other than a necessary wavelength is within the scope of the disclosure.
  • photocatalyst refers to substances exhibiting a photocatalytic activity by exposure of light having an energy higher than a predetermined band gap.
  • the photocatalyst may be a visible light photocatalyst, non-limiting examples of which include 4CzIP, CZS1, CzS2, 2Cz- DPS, 2TCz-DPSN, fac-Ir(ppy) 3 , [Ir(ppy)2(dtbbpy)]PF 6 , [Ir(dF(CF 3 )ppy) 2 (bpy)]PF 6 , [Ir(dF(CF 3 )ppy) 2 (dtbbpy)]PF 6 , [Ir(dF(Me)ppy) 2 (bpy)]PF 6 , [Ir(F(Me)ppy) 2 (bpy)]PF 6 , [Ru(bpy) 3 ](PF 6 ) 2 , [Acr-Mes]ClO 4 , Eosin Y, and Rose Bengal.
  • 4CzIP CZS1, CzS2, 2Cz- DPS
  • 2TCz-DPSN fac-
  • the photocatalyst may be one or a combination of metal oxide semiconductors, such as – for instance and without limitation - titanium oxide, tungsten oxide, zinc oxide, tin oxide, iron oxide, bismuth oxide, bismuth vanadate and strontium titanate.
  • metal oxide semiconductors such as – for instance and without limitation - titanium oxide, tungsten oxide, zinc oxide, tin oxide, iron oxide, bismuth oxide, bismuth vanadate and strontium titanate.
  • photochemical conditions refers to using a source of light or near-visible electromagnetic radiation to promote a reaction.
  • Salts of the compounds disclosed herein are within the scope of the present disclosure. Salts include both acid and base addition salts.
  • “Acid addition salt” refers to salts formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, carbonic acid, phosphoric acid, and organic acids selected from aliphatic, cycloaliphatic, aromatic, araliphatic, heterocyclic, carboxylic, and sulfonic classes of organic acids such as formic acid, acetic acid, propionic acid, glycolic acid, gluconic acid, lactic acid, pyruvic acid, oxalic acid, malic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, aspartic acid, ascorbic acid, glutamic acid, anthranilic acid, benzoic acid, cinnamic acid, mandelic acid, embonic acid, phenylacetic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, and salicycl
  • Base addition salt refers to salts formed with an organic or inorganic base.
  • the term “predominantly” means greater than 50%, at least 75%, at least 90% or at least 95% on a population%, w/w%, w/v% or v/v% b
  • the term “chemical processing aid” means a chemical added directly to the reaction mixture or is present in a mixture and is used to aid in processing and its function is such that it does not remain in the product.
  • transition metal catalyst refers to a substance containing at least one element from groups III through XI of the periodic table which exhibits catalytic activity.
  • Non limiting examples include iron catalysts, nickel catalysts, palladium catalysts, platinum catalysts, or copper catalysts.
  • Non limiting examples of iron catalysts where X stands for halogen include Fe, FeX 2 , FeX 3 , Fe(acac) 3 , Fe(NO 3 ) 3 , or Fe(OTf) 3 .
  • Non limiting examples of nickel catalysts include Raney Ni, Ni/C, Ni/Si Ni, NiX 2 , NiX 2 •nH 2 O, NiX 2 (DME), NiX 2 (diglyme), (bpy)NiX2, , Ni(OTf) 3 , Ni(acac) 2 , Ni(COD) 2 , Ni(CO) 4 , (dppe)NiX 2 , (dppp)NiX 2 , (dppb)NiX 2 , (dppf)NiX 2 , (dcype)NiX 2 , (dcypp)NiX 2 , (dcypb)NiX 2 , (binap)NiX 2 , (bpy)NiX 2 or solvates thereof.
  • Non limiting examples of palladium catalysts where X stands for halogen include Pd, Pd/C, Pd/Si, Pd/BaSO 4 , Pd(dba) 2 , Pd 2 (dba) 3 , Pd(PPh 3 ) 4 PdX 2 , Pd(OAc) 2 , Pd(OBz) 2 , [Pd(allyl)X] 2 , Pd(MeCN) 2 X 2 , (COD)PdX 2 , (2-methylallyl)palladium chloride dimer, Pd(OTf) 2, (PPh 3 ) 2 PdX 2 , (PCy 3 )PdX 2 ,(PtBu 3 ) 2 Pd, Pd[(o-tol) 3 P] 2, trans-Di( ⁇ -acetato)bis[o-(di-o-tolyl- phosphino)benzyl]dipalladium(II), Pd(amphos)X 2
  • Non limiting examples of copper catalysts where X stands for halogen include CuX, CuX 2 , CuCN, Cu(OTf) 2 ,CuO, Cu 2 O, CuBr•DMS or solvates thereof.
  • the transition metal catalyst may act as a precursor to an active catalyst species which optionally may be preformed and charged into the reaction or generated in situ.
  • the transition metal catalyst is optionally used with a ligand.
  • the ligand may optionally be precomplexed with the transition metal before addition into the reaction or the ligand and transition metal catalyst complexed in situ.
  • the transition metal catalyst may be used alone or in combination with any of the preceding transition metal catalysts.
  • diphosphine ligand refers to a substance containing two phosphino groups connected by a backbone.
  • the diphosphine ligand is able to chelate to a transition metal catalyst in a bidentate fashion.
  • Non limiting examples include 1,1-bis(diphenylphosphino)methane, 1,2- bis(diphenylphosphino)ethane, 1,3-bis(diphenylphosphino)propane, 1,4- bis(diphenylphosphino)butane, O-isopropylidene-2,3-dihydroxy-1,4- bis(diphenylphosphino)butane, 2,3-bis(diphenylphosphino)butane, 2,2'- bis(diphenylphosphino)-1,1'-binaphthyl, 1,2-Bis(diphenylphosphino)benzene, 4,5- Bis(diphenylphosphino)-9,9-dimethylxanthene, bis[(2-diphenylphosphino)phenyl] ether, 4,4'-bi-1,3-benzodioxole-5,5'-diylbis(diphenyl
  • the diphosphonium salts are hydrochloride, hydrobromide, hydroiodide, tetrafluoroborate salts or some combination thereof.
  • the diphosphine ligand may optionally be added separately from the transition metal catalyst or added precomplexed to the transition metal catalyst.
  • the diphosphine may optionally in situ be oxidized to the monophosphine oxide, which acts as the ligand for an active catalyst species.
  • the diphosphine ligand may be used alone or in combination with any of the preceding diphosphine ligands.
  • the process comprises forming a reaction mixture comprising compound 223 (3-acetyldihydrofuran-2(3H)-one), CH 3 Cl, an alkali metal iodide, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 775 (3-acetyl-3-methyldihydrofuran-2(3H)- one).
  • CH 3 Cl is present in a stoichiometric excess with respect to compound 223.
  • the alkali metal iodide is selected from NaI, KI, and LiI. In some such aspects, the alkali metal iodide is KI.
  • the base is an inorganic base. In some such aspects, the base is a weak inorganic base. In some such aspects, the base is a carbonate. In some such aspects, the base is selected from sodium carbonate, sodium bicarbonate, potassium carbonate, and potassium bicarbonate. In some aspects, the base may be present in a stoichiometric excess with respect to compound 223.
  • the solvent system comprises or predominantly comprises an aprotic solvent.
  • a suitable solvent can be selected from among acetone, methyl t-butyl ether, acetonitrile, 1,4-dioxane, tetrahydrofuran, and isopropyl acetate.
  • the solvent system comprises acetonitrile, or the solvent system comprises acetone.
  • the solvent system comprises or predominantly comprises acetone.
  • the reaction is run at reflux. The reaction may be monitored for completion by methods known in the art such as 1 H NMR (CDCl 3 ), high performance liquid chromatography (“HPLC”), or ultraperformance liquid chromatography (“UPLC”).
  • the process for preparing compound 775 provides for good selectivity and yield to compound 775.
  • the process for preparing compound 775 provides for elimination of certain expensive and hazardous reagents known in the art, such as MeI, organic bases such as sodium amylate or sodium methoxide, and sodium metal.
  • Some aspects of the disclosure are directed to a process for the preparation of compound 200 (1-methylcyclopropane-1-carboxylic acid) according to a first scheme, a second scheme, or a third scheme.
  • Various methods for cyclopropanation are known in the prior art. See Ebner, et al., ”Cyclopropanation Strategies in Recent Total Synthesis”, Chem. Rev.
  • the first scheme for preparing compound 200 comprises three steps.
  • Step 1 of the first scheme for preparing compound 200 comprises forming a reaction mixture comprising compound 775 (3-acetyl-3- methyldihydrofuran-2(3H)-one), HCl, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 069 (5-chloro-3- methylpentan-2-one) according to the following reaction scheme: [138]
  • HCl is concentrated HCl.
  • the HCl is hydrogen chloride gas.
  • the solvent system comprises or predominantly comprises an aprotic solvent, water, or a combination thereof.
  • the aprotic solvent is DCM.
  • the solvent system comprises less than 70 w/w% water.
  • Step 2 of the first scheme for preparing compound 200 comprises forming a reaction mixture comprising compound 069, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 079 (methyl-(1-methylcyclopropyl)-ketone) according to the following reaction scheme [140]
  • the base is a strong inorganic base.
  • the base is an alkali metal hydroxide.
  • the base is selected from sodium hydroxide and potassium hydroxide.
  • the solvent system comprises or predominantly comprises a polar protic solvent, water, or a combination thereof.
  • Step 3 of the first scheme for preparing compound 200 comprises forming a reaction mixture comprising compound 079, an oxidizing agent, optionally a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 200 according to the following reaction scheme [143]
  • the oxidizing agent is selected from sodium hypochlorite, sodium hypobromite, bromine, or chlorine.
  • the oxidizing agent is sodium hypochlorite.
  • the concentration of sodium hypochlorite is as obtained in a commercially available solution.
  • optionally a base is present.
  • the base is selected from sodium hydroxide or potassium hydroxide.
  • the solvent system comprises or predominantly comprises water.
  • any of compounds 775, 069, 079, and 200 are optionally isolated from the reaction product mixture.
  • any two, or all, of the sequential reactions from compound 223 to compound 775, from compound 775 to compound 069, from compound 069 to compound 079, and from compound 079 to compound 200, are carried forward to the next step without isolation or purification.
  • the second scheme for preparing compound 200 comprises two steps.
  • Step 1 of the second scheme for preparing compound 200 comprises forming a reaction mixture comprising compound 900, CHX 3 , a base, a solvent system, and a phase transfer catalyst (PTC), and reacting the reaction mixture to form a reaction product mixture comprising compound 905 according to the following reaction scheme
  • R is selected from CO 2 CH 3 , CO 2 CH 2 CH 3 , COOH, and CN.
  • R may be CO2CH3 or CO2CH2CH3.
  • Each X is independently selected from Cl, Br, and I.
  • each X is Cl; when R is CO 2 CH 3 , CO 2 CH 2 CH 3 , or CN, the process further comprises Step 1b forming a reaction mixture comprising compound 905, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 906 according to the following reaction scheme ; Step 2 comprises forming a reaction mixture comprising compound 906, a reducing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 200 according to the following reaction scheme
  • the process comprises Step 2’, Step 2’ comprising forming a reaction mixture comprising compound 905, a reducing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 200 according to the following scheme [150]
  • the base is a strong inorganic base.
  • the base is an alkali metal hydroxide.
  • the base is selected from sodium hydroxide and potassium hydroxide.
  • the base is present in molar excess over compound 900.
  • the CHX 3 reagent is chloroform, bromoform, or iodoform. In one aspect, the CHX 3 reagent is chloroform.
  • PTC Phase transfer catalysts
  • the PTC is selected from ammonium halide salts, crown ethers, and PEGs.
  • suitable PTCs include triethylbenzylammonium chloride, triethylbenzylammonium bromide, tetraethylammonium bromide, tetrabutylammonium bromide, and ethyltrimethylammonium iodide.
  • the PTC is triethylbenzylammonium chloride.
  • the PTC is generally present in a catalytic amount.
  • suitable solvents include protic solvents, aprotic solvents, and combinations thereof.
  • suitable solvents include water, hexane, pentane, heptane, benzene, toluene, chlorobenzene, dichloromethane, and combinations thereof.
  • the reaction temperature may be suitably selected to achieve desired purity and yield in a commercially acceptable time. Reaction completion may suitably be measured by in-process testing as described elsewhere herein.
  • the process further comprises Step 1b forming a reaction mixture comprising compound 905, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 906 according to the following reaction scheme.
  • the base is a strong inorganic base.
  • the base is an alkali metal hydroxide.
  • the base is selected from sodium hydroxide and potassium hydroxide.
  • the solvent system suitably comprises or predominantly comprises a polar protic solvent.
  • the solvent system comprises or predominantly comprises a C 1-4 alcohol, such as methanol or ethanol. In some aspects, the solvent system comprises methanol. In some such aspects, the solvent system comprises water. In some such aspects, the solvent system comprises water and a C 1-4 alcohol mixture.
  • the reaction product mixture may be optionally worked up. For instance, water may be added and the pH adjusted to less than 3, such as about 1-2, with a strong acid such as HCl. The resultant mixture may be extracted with a solvent, such as a non-polar solvent (e.g., toluene) to extract compound 906. The extraction mixture may then be optionally evaporated (e.g., under vacuum) to isolate compound 906.
  • Step 2 of the second scheme for preparing compound 200 comprises forming a reaction mixture comprising compound 906, a reducing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 200 according to the following reaction scheme .
  • the transformation of compound 906 to compound 200 is carried out under hydrodehalogenation conditions, comprising forming a reaction mixture comprising compound 906, H 2 , a metal catalyst, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 200.
  • Reaction temperature and pressure may be suitably selected to achieve commercially acceptable yield, purity, and throughput.
  • a suitable solvent is selected from among methanol, ethanol, 1-propanol, isopropanol, t-butanol, isobutanol, sec-butanol, 1-hexanol, 2- ethyl-1-hexanol, 2-octanol, benzyl alcohol, n-octane, cyclohexane, xylene, tetrahydrofuran, dioxane, water, monoglyme, diglyme, ethyleneglycol, N,N- dimethylformamide, N,N-dimethylsulfoxide, triethylamine, pyridine, and combinations thereof.
  • the solvent system comprises a polar protic solvent.
  • the polar protic solvent comprises a C 1-4 alcohol.
  • the solvent is t-butanol.
  • the reaction mixture comprises a base. Suitable bases include sodium hydroxide, potassium hydroxide, lithium hydroxide, calcium hydroxide, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, sodium ethoxide, potassium ethoxide, sodium tert-butoxide, potassium tert-butoxide, triethylamine, pyridine, ethylenediamine, and combinations thereof.
  • the base is an alkali metal hydroxide.
  • the base is selected from sodium hydroxide and potassium hydroxide. In some aspects, the base is an alkali metal alkoxide. In some aspects, the base is selected from sodium tert-butoxide and potassium tert-butoxide. In some aspects, the base is potassium tert-butoxide. In some aspects, the base is in molar excess over compound 906. [163] In some aspects, the metal catalyst is a Pt, Pd, Rh, or Ru catalyst. In some aspects, the metal catalyst is Pd/C, Rh/Al 2 CO 3 , Pd/CaCO 3 , Pd/Pb/CaCO 3 , or Pt/Al 2 O 3 . In one aspect, the metal catalyst is Pd/C.
  • the reaction product mixture may be optionally worked up. For instance, and without limitation, the reaction product mixture may be filtered and the filtrate may be evaporated to remove solvent. The resulting mixture may be diluted with water and acidified with strong acid (e.g., HCl) to a pH of less than 3, such as from about 1 to about 2. The resultant mixture may be extracted with a solvent (e.g., DCM) to extract compound 200. In some aspects, compound 200 may be isolated by evaporation of the solvent to yield compound 200.
  • strong acid e.g., HCl
  • a solvent e.g., DCM
  • the transformation of compound 905 to compound 200 is carried out under reducing metal conditions, comprising forming a reaction mixture comprising compound 905, a reducing metal, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 200.
  • the solvent system comprises a polar aprotic solvent, a polar protic solvent, or a combination thereof.
  • the solvent system may suitably comprise or predominantly comprise a polar aprotic solvent.
  • the solvent is tetrahydrofuran (THF).
  • the solvent system comprises or predominantly comprises a polar aprotic solvent (e.g., THF) and a polar protic solvent (such as a C 1-4 alcohol (e.g., methanol or ethanol)), water, and combinations thereof.
  • the reducing metal is Na, K, Ca, Mg, or zinc.
  • the reducing agent is selected form Na and Zn.
  • the reducing agent is sodium metal.
  • the reducing agent is in molar excess over compound 905.
  • the solvent is acetic acid.
  • a base is optionally present.
  • the base is an inorganic base.
  • the base is an alkali metal hydroxide.
  • the base is selected from sodium hydroxide and potassium hydroxide.
  • the base can also be used as a solvent, for example, triethylamine.
  • the base is in molar excess over compound 905 from step 1.
  • the reducing agent may be added in portions during the course of the reaction. In some aspects, the reducing agent may be added continuously or semi-continuously during the course of the reaction.
  • Compound 200 may be isolated by methods known in the art such as solvent removal.
  • the reaction product mixture may be optionally worked up. For instance, a solution containing compound 200 may be acidified, extracted with a solvent and isolated by methods known in the art.
  • any of compounds 905, compound 906, and 200 are optionally isolated from the reaction product mixture.
  • any two, or all, of the sequential reactions from compound 900 to compound 905, from compound 905 to compound 906, and from compound 906 to compound 200 are carried forward to the next step without isolation or purification.
  • the third scheme for preparing compound 200 comprises two steps.
  • Step 1 of the third scheme for preparing compound 200 comprises forming a reaction mixture comprising acetic acid, compound 100 (methyl 4-chloro- 2-methylenebutanoate), a base, a photocatalyst, and a solvent system, and reacting the reaction mixture by exposure to light emitted from at least one light emitting source to form a reaction product mixture comprising compound 110 (methyl 1- methylcyclopropane-1-carboxylate) according to the following reaction scheme [174]
  • the solvent system may suitably comprise or predominantly comprises a polar or nonpolar solvent.
  • the solvent system comprises a polar aprotic solvent or the solvent system comprises dimethyl formamide (DMF).
  • the polar solvent comprises or predominantly comprises DMF.
  • the base is an inorganic base. In some such aspects, the base is a carbonate. In some such aspects, the base is Cs 2 CO 3 . In some aspects, the base is an organic base. [176] In some aspects, the photocatalyst is a visible light photocatalyst.
  • Non-limiting examples of photocatalysts within the scope of the disclosure include 4CzIP, CZS1, CzS2, 2Cz-DPS, 2TCz-DPSN, fac-Ir(ppy) 3 , [Ir(ppy)2(dtbbpy)]PF 6 , [Ir(dF(CF 3 )ppy) 2 (bpy)]PF 6 , [Ir(dF(CF 3 )ppy) 2 (dtbbpy)]PF 6 , [Ir(dF(Me)ppy) 2 (bpy)]PF 6 , [Ir(F(Me)ppy) 2 (bpy)]PF 6 , [Ru(bpy) 3 ](PF 6 ) 2 , [Acr- Mes]ClO 4 , Eosin Y, and Rose Bengal.
  • the photocatalyst is 4CzIP or Ir(ppy) 2 (dtbbpy)PF 6 .
  • the light source is a blue light emitting diode.
  • Step 2 of the third scheme for preparing compound 200 comprises forming a reaction mixture comprising compound 110, a solvent system, and a base, and reacting the reaction mixture to form a reaction product mixture comprising compound 200 according to the following reaction scheme .
  • the base is an inorganic base.
  • the base is an alkali metal hydroxide.
  • the base is selected from sodium hydroxide and potassium hydroxide.
  • the solvent system suitably comprises or predominantly comprises a polar solvent.
  • the solvent system comprises or predominantly comprises a C 1-4 alcohol, such as methanol or ethanol.
  • the solvent system comprises water.
  • the solvent system comprises water and C 1-4 alcohol mixture.
  • the reaction product mixture may be optionally worked up. For instance, water may be added and the pH adjusted to less than 3, such as about 1-2, with a strong acid such as HCl.
  • the resultant mixture may be extracted with a solvent, such as a non-polar solvent (e.g., toluene) to extract compound 200.
  • the extraction mixture may then be optionally evaporated (e.g., under vacuum) to yield compound 200.
  • compounds 110 and 200 are optionally isolated from the reaction product mixture.
  • Step 1 comprises substep (a) comprising forming a reaction mixture comprising compound 200 (1-methylcyclopropanecarboxylic acid), a chlorinating reagent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising an acid chloride intermediate, followed by substep (b) comprising forming a reaction mixture by combining the reaction product mixture from substep (a) with an ammonia source and reacting the reaction mixture to form a reaction product mixture comprising compound 144 (1-methylcyclopropane carboxamide) according to the following reaction scheme [185]
  • the solvent system comprises or predominantly comprises an aprotic solvent.
  • the solvent system comprises or predominantly comprises dichloromethane (DCM), toluene, acetonitrile or a combination thereof.
  • the substep (a) reaction mixture may further comprise a catalyst selected from DMF, 4-Dimethylaminopyridine (DMAP), triethylamine, N-Methyl-2-pyrrolidone (NMP), N-methylformanilide, N- formylpyridine, or pyridine.
  • the chlorinating reagent may be selected from thionyl chloride, triphosgene, or phosgene. In some such aspects, the chlorinating agent is thionyl chloride.
  • the substep 1b solvent system predominantly comprises the solvent system from step 1a. In some aspects, the substep 1b solvent system predominantly comprises the combination of the solvent system from step 1a and a polar protic solvent. In some aspects, the substep 1b solvent system predominantly comprises a polar protic solvent. In either such aspect, the polar protic solvent may suitably be water, C 1-4 alcohol or a combination thereof, such as water, methanol, ethanol, or a combination thereof.
  • the ammonia source is selected from ammonia, ammonium hydroxide, and ammonia dissolved in a suitable organic solvent known in the art, such as methanol, ethanol, DCM, or toluene. In some such aspects, the ammonia source is selected form ammonia and ammonium hydroxide. In some aspects, ammonia is in molar excess to compound 200.
  • the acid solution of compound 144 is added to the source of ammonia. In some aspects, the source of ammonia may be added to the reaction mixture.
  • Compound 144 may be optionally isolated from the reaction mixture by methods known in the art, such as solvent removal or filtration.
  • Step 2 comprises substep (a) comprising forming a reaction mixture comprising compound 144, a base, an oxidant, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising a N- halocarboxamide intermediate, followed by substep (b) comprising heating the reaction product mixture comprising the N-halocarboxamide intermediate to form a reaction product mixture comprising compound 070 (1-methylcyclopropylamine) according to the following reaction scheme [193]
  • the oxidant is selected from Cl 2 , NaOCl, Br 2 , and NaOBr.
  • the oxidant is NaOCl.
  • the oxidant is Br 2 .
  • the base is an inorganic base. In some such aspects, the base is an alkali metal hydroxide. In some such aspects, the base is selected from sodium hydroxide and potassium hydroxide. In some aspects, the base is present in molar excess over compound 144.
  • the solvent system comprises or predominantly comprises a polar protic solvent. In some such aspects, the solvent system comprises or predominantly comprises water. In some such aspects, compound 144 is slurried in the solvent system.
  • a quenching reagent may be added to the reaction product mixture to quench the excess oxidant. In some aspects, the quenching agent is Na 2 S 2 O 3 .
  • a representative example of the order of some of the reaction steps for certain acrylate-derived cyclopropyl compounds may be ordered as depicted below
  • reaction of compound 351 to form compound 110 may proceed according to the following reaction scheme .
  • the reaction of compound 351 to form compound 110 may proceed according to conditions known in literature for dehalogenation of alkanes.
  • the reaction of compound 110 to form compound 200 may proceed according to the following reaction scheme .
  • the reaction of compound 110 to form compound 144 may proceed according to the following reaction scheme .
  • the reaction of compound 110 to form compound 144 may proceed according to conditions known in literature for ammonolysis of organic esters to amides.
  • the reaction of compound 351 to form compound 145 may proceed according to the following reaction scheme .
  • the reaction of compound 351 to form compound 145 may proceed according to conditions known in literature for ammonolysis of esters to amides.
  • the reaction of compound 350 to form compound 145 may proceed according to the following reaction scheme .
  • the reaction of compound 350 to form compound 145 may proceed according to conditions known in literature for ammonolysis of carboxyl groups to amides.
  • the reaction of compound 145 to form compound 146 may proceed according to the following reaction scheme .
  • the reaction of compound 145 to form compound 144 may proceed according to the following reaction scheme .
  • the reaction of compound 146 to form compound 070 may proceed according to the following reaction scheme .
  • Step 1 comprises forming a reaction mixture comprising compound 079, a source of hydroxylamine, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 994 (1-(1- methylcyclopropyl)ethan-1-one oxime) according to the following reaction scheme .
  • the source of amine is selected from hydroxylamine and hydroxylamine salts.
  • the hydroxylamine salt is the HCl salt.
  • the base is selected from an inorganic base or an organic base.
  • the base is sodium acetate or potassium acetate.
  • the solvent system comprises or predominantly comprises a polar protic solvent. In some such aspects, the solvent system comprises or predominantly comprises a C 1-4 alcohol. In one aspect, the solvent system comprises or predominantly comprises methanol or ethanol.
  • the reaction product mixture comprises (E,Z)-1-(1- methylcyclopropyl)ethan-1-one oxime. In some aspects, the reaction product mixture comprises (E)-1-(1-methylcyclopropyl)ethan-1-one oxime. In some aspects, the reaction product mixture comprises (Z)-1-(1-methylcyclopropyl)ethan-1-one oxime.
  • Step 2 comprises forming a reaction mixture comprising compound 994, an activator, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 403 (N-(1-methylcyclopropyl) acetamide) according to the following reaction scheme [218]
  • the activator is selected from tosyl chloride, cyanuric hydrochloride, thionyl chloride, sulfamic acid, phosphorus pentachloride, phosphorus pentoxide, triethylamine, inorganic bases, inorganic acids, organic acids, trimethylsilyl iodide, transition metal catalysts (such as zinc chloride), thiamine hydrochloride, alkylpyridinium salts, chloral, and combinations thereof.
  • the activator is selected from tosyl chloride, cyanuric hydrochloride, thionyl chloride, and sulfamic acid. In some such aspects, the activator is tosyl chloride [219] In some aspects, the solvent system comprises or predominantly comprises a polar or nonpolar solvent. In some such aspects, the solvent system comprises or predominantly comprises acetonitrile. [220] Step 3 comprises forming a reaction mixture comprising compound 403, an acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 070 according to the following reaction scheme . [221] In some aspects, the acid is selected from an inorganic acid or an organic acid.
  • the acid is selected from among hydrochloric acid, sulfuric acid, phosphoric acid, acetic acid, and TsOH.
  • the acid is a mineral acid.
  • the acid is H 2 SO 4 .
  • the solvent system comprises or predominantly comprises a polar protic solvent.
  • the solvent system comprises or predominantly comprises water.
  • any of compounds 994, 403, and 070 are optionally isolated from the reaction product mixture.
  • two, or all, of the sequential reactions from compound 079 to compound 070 are carried forward onto the next step without isolation or purification.
  • compound 070 may be prepared from acetonitrile according to the following reaction scheme
  • the ethyl magnesium halide reagent may be suitably selected from ethyl magnesium bromide and ethyl magnesium chloride.
  • the solvent may be suitably selected from diethyl ether, tetrahydrofuran, 2-methyltetrahydrofuran, methyl tert-butyl ether, tert-amyl methyl ether, and cyclopentyl methyl ether.
  • the titanium reagent is selected from titanium(IV) methoxide, titanium(IV) ethoxide, titanium(IV) propoxide, titanium(IV) isopropoxide, titanium(IV) butoxide, titanium(IV) tert-butoxide, titanium(IV) 2-ethylhexyloxide, and methyltitanium(IV) triisopropoxide.
  • the acid is a Lewis acid or a Bronsted acid.
  • the Lewis acid is selected from boron trifluoride, boron trifluoride diethyl etherate, boron trifluroride tetrahydrofuran complex, boron trifluoride dibutyl etherate, boron trifluoride tert-butyl methyl etherate, boron trichloride, titanium(IV) chloride, aluminum trichloride, cerium(III) trichloride heptahydrate, zinc chloride, nickel(II) bromide trihydrate.
  • the Bronsted acid is selected from sulfuric acid, phosphoric acid, and acetic acid.
  • a challenge in using this chemistry to form cyclopropanamines is the large amount of metal salts present in the reaction mass, which causes significant difficulty in post-reaction workup and product isolation steps.
  • polar cyclopropanamine products are water soluble and a typical extractive workup used to remove inorganic salts will result in significant product loss to the aqueous layer.
  • Another challenge is the insoluble titanium dioxide that forms during post-reaction workup which coats reactor vessel walls and requires aggressive reactor cleanout protocols to remove. (Org. Process Res. Dev.2021, 25, 2351; Org. Process Res. Dev. 2020, 24, 1735-1742; Org. Process Res. Dev.2012, 16, 836).
  • a chemical processing aid is added after the reaction to facilitate product isolation.
  • the chemical processing aid is selected from tartrate salts, such as potassium sodium tartrate, lactate salts, glycolate salts, ethylenediaminetetraacetate salts, triethanolamine, and citrate salts.
  • the salts are generated from the corresponding acid upon treatment with a base.
  • the processing aid is a flocculent.
  • the flocculent is selected from aluminum sulfate, ferric chloride, ferrous sulfate, ferric sulfate, sodium silicate, silicate salts, and silicate/kaolin clays or hydrates thereof.
  • Step 1 comprises forming compound 181a (2-(bromomethyl)-1- chloro-3-nitrobenzene) by forming a reaction mixture comprising compound 339 (1- chloro-2-methyl-3-nitrobenzene), a source of Br, optionally a photosensitive radical initiator, and a solvent system, and reacting the reaction mixture under photochemical conditions to form a reaction product mixture comprising compound 181a according to the following reaction scheme .
  • the source of Br is selected from N- bromosuccinimide, Br 2 , or the combination of HBr and H 2 O 2 . In some aspects, the source of Br is N-bromosuccinimide.
  • the solvent system comprises or predominantly c system comprises or predominantly comprises dichloromethane (DCM) or a combination of DCM and water.
  • the reaction is promoted by a light source. In some aspects, the photochemical conditions relate to promoting the reaction using a visible light source. In some such aspects, the visible light is provided by about 400W of a light source. [236] In some aspects, a photosensitive or thermally activated radical initiator is used.
  • Step 2 comprises forming compound 378 by the (i) the combination of steps 2(a) and 2(b) or by (ii) step 2.
  • Step 2(a) comprises forming a reaction mixture comprising compound 181a, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 050 ((2-chloro-6- nitrophenyl)methanol) according to the following reaction scheme
  • the base is a weak base.
  • the base is an inorganic base.
  • the base is a carbonate or a bicarbonate.
  • the base is selected from sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, and magnesium carbonate.
  • the solvent system comprises or predominantly comprises at least one polar solvent system. In some such aspects, the solvent system comprises or predominantly comprises water. In some such aspects, the solvent system comprises or predominantly comprises acetonitrile. In some such aspects the solvent system comprises acetonitrile and water.
  • Step 2(b) comprises forming a reaction mixture comprising compound 050, an oxidizing reagent, a PTC, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 378 (2- chloro-6-nitro benzaldehyde) according to the following reaction scheme oxidizing reagent
  • the oxidizing reagent is NaOCl.
  • the phase transfer catalyst (PTC) is a quaternary ammonium salt.
  • the PTC is tetrabutylammonium bromide.
  • the solvent system comprises or predominantly comprises a non-polar solvent.
  • the solvent system comprises or predominantly comprises toluene.
  • Step 2 comprises forming a reaction mixture comprising compound 181a ((2-(bromomethyl)-1-chloro-3-nitrobenzene), an oxidizing reagent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 378 according to the following reaction scheme .
  • the oxidizing reagent is a N-oxide reagent.
  • the reagent is trimethylamine-N-oxide or N-methylmorpholine N-oxide.
  • the solvent system comprises or predominantly comprises at least one polar solvent.
  • the solvent system comprises or predominantly comprises DMSO or DMF.
  • Step 3 comprises forming a reaction mixture comprising compound 378, 3-aminopyridine, an acid catalyst, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 003a (1- (2-chloro-6-nitrophenyl)-N-(pyridine-3-yl)methanimine) according to the following reaction scheme .
  • the solvent system comprises or predominantly comprises a non-polar solvent.
  • the solvent system comprises or predominantly comprises toluene.
  • the acid is an organic acid. In some such aspects the acid is p-toluenesulfonic acid.
  • Step 4 comprises forming a reaction mixture comprising compound 003a, a phosphine or a phosphite, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 093a according to the following reaction scheme
  • the solvent system comprises or predominantly comprises a polar protic solvent or a nonpolar solvent. In some such aspects, the solvent system comprises or predominantly comprises a C 1-4 alcohol. In one such aspect, the solvent system comprises or predominantly comprises isopropyl alcohol. In some aspects, the solvent system comprises or predominantly comprises toluene.
  • the phosphine or phosphite is trimethyl phosphite, triethyl phosphite, triisopropyl phosphite, triphenylphosphite, trimethyl phosphine, triethyl phosphine, tributyl phosphine, or triphenyl phosphine.
  • the reaction is run at reflux.
  • any of compounds 181a, 050, 378, 003a, and 093a are optionally isolated from the reaction product mixture.
  • any two sequential reactions, or all of the sequential reactions from compound 339 to compound 093a are done in a telescopic pot scheme.
  • Some aspects of the disclosure are directed to a process for the preparation of compound 093a, the process comprising seven steps.
  • Step 1 comprises forming a reaction mixture comprising compound 150 (2,6-dichlorobenzaldehyde), an acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 086 (1- (2,6-dichlorophenyl)-N-(pyridin-3-yl)methanimine) according to the following reaction scheme
  • the acid is p-toluenesulfonic acid.
  • the solvent system comprises or predominantly comprises at least one non-polar solvent. In some such aspects, the solvent system comprises or predominantly comprises toluene.
  • Step 2 comprises forming a reaction mixture comprising compound 086, a reducing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 084 (N-(2,6-dichlorobenzyl)pyridin-3-amine) according to the following reaction scheme .
  • the reducing agent is selected from sodium borohydride and sodium cyanoborohydride.
  • Step 3 comprises forming a reaction mixture comprising compound 084, a reagent for converting an amine moiety to a nitrosamine moiety, an acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 085 (N-(2,6-dichlorobenzyl)-N-(pyridin-3-yl)nitrous amide) according to the following reaction scheme .
  • the reagent for conversion of an amine to a nitrosamine is a nitrite.
  • the reagent for conversion of an amine to a nitrosamine is sodium nitrite.
  • the acid is an organic acid. In some such aspects, the acid is p-toluenesulfonic acid.
  • the solvent system comprises or predominantly comprises at least one polar aprotic solvent. In some such aspects, the solvent system comprises or predominantly comprises DCM.
  • Step 4 comprises: (a) forming a reaction mixture comprising compound 085, a reductant, a base, and a solvent system, and reacting the reaction mixture and (b) acidification to form a reaction product mixture comprising compound 048 (1-[(2,6-dichlorophenyl)methyl]-1-(3-pyridyl)hydrazine salt) according to the following reaction scheme [268]
  • the reductant is thiourea dioxide.
  • the base is an inorganic base.
  • the base is an alkali metal hydroxide.
  • the base is NaOH or KOH.
  • the solvent system comprises or predominantly comprises at least one polar protic solvent.
  • the solvent system comprises or predominantly comprises water.
  • the acid is an inorganic acid.
  • the acid is HCl.
  • the acid is HCl in isopropanol and compound 048 is (3- (1-(2,6-dichlorobenzyl)hydrazineyl)pyridine ⁇ HCl).
  • Step 5 comprises forming a reaction mixture comprising compound 048, acetic anhydride, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 083 (N'-(2,6- dichlorobenzyl)-N'-(pyridin-3-yl)acetohydrazide) according to the following reaction scheme.
  • the base is an organic base. In some such aspects, the base is triethylamine.
  • the solvent system comprises or predominantly comprises at least one polar aprotic solvent. In some such aspects, the solvent system comprises or predominantly comprises dichloromethane.
  • Step 6 comprises forming a reaction mixture comprising compound 083, a ligand, a transition metal catalyst, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 082 (1-[4-chloro-2-(3-pyridyl)-3H-indazol-1-yl]ethanone) according to the following reaction scheme.
  • the ligand is ethylene diamine or trans- dimethylcyclohexyl-1,2-diamine.
  • the transition metal catalyst is selected from Group VIII, Group IX, Group X, or Group XI metals. In some aspects, the transition metal catalyst is selected from a Pd catalyst and a Cu catalyst. In some aspects, the transition metal catalyst is CuI.
  • the base is an inorganic base. In some such aspects, the base is K 3 PO 4 .
  • the solvent system comprises or predominantly comprises at least one non-polar solvent. In one aspect, the solvent system comprises predominantly comprises dioxane. In another aspect, the solvent system predominantly comprises toluene.
  • Step 7 comprises forming a reaction mixture comprising compound 082, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 093a according to the following reaction scheme
  • the base is an inorganic base.
  • the base is a weak inorganic base.
  • the base is a carbonate.
  • the base is selected from sodium carbonate, sodium bicarbonate, potassium carbonate, and potassium bicarbonate.
  • the solvent system comprises or predominantly comprises a polar protic solvent.
  • the solvent system comprises or predominantly comprises a C 1-4 alcohol.
  • the solvent system comprises or predominantly comprises methanol.
  • reactions steps 6 and 7 are done sequentially in a single vessel.
  • Some aspects of the disclosure are directed to a process for the preparation of compound 093a, the process comprising three steps.
  • a reaction mixture solution is formed comprising compound 150 (2,6-dichlorobenzaldehyde), acetohydrazine, a solvent system, and an organic acid, and the reaction mixture is reacted to form a reaction product mixture comprising compound 197 (N-[(2,6-dichlorophenyl)methyleneamino]acetamide) according to the following reaction scheme Step 1 197 .
  • the organic acid is p-toluenesulfonic acid.
  • the solvent system comprises at least one nonpolar solvent. In some such aspects, the solvent system comprises toluene.
  • the reaction is run at reflux with azeotropic distillation of water to drive the condensation process.
  • a reaction mixture is formed comprising compound 197, a reducing agent, and a solvent system, and the reaction mixture is reacted to form a reaction product mixture comprising compound 040 (N'-[(2,6- dichlorophenyl)methyl]acetohydrazide) according to the following reaction scheme Step 2 040 .
  • the reducing agent is magnesium or a borohydride.
  • the reducing agent is selected from sodium borohydride, sodium cyanoborohydride, and magnesium.
  • the solvent system comprises at least one alcohol, at least one carboxylic acid, or a combination thereof. In some such aspects, the solvent system comprises methanol, ethanol, acetic acid, or a combination thereof.
  • a reaction mixture is formed comprising compound 040, 3-bromopyridine, a ligand, a transition metal catalyst, and a solvent system, and the reaction mixture is reacted to form a reaction product mixture comprising compound 093a according to the following reaction scheme
  • the ligand is a diamine ligand. In some such aspects the ligand is selected from trans-N,N’-dimethylcyclohexyldiamine and N,N’- dimethylethylenediamine.
  • the transition metal catalyst is a copper catalyst. In some such aspects, the transition metal catalyst is CuI.
  • the solvent system comprises a nonpolar solvent. In some such aspects, the solvent system comprises toluene.
  • Some aspects of the disclosure are directed to a process for the preparation of compound 093a or 093b (4-chloro-2-(3-pyridyl)indazole or 4-bromo-2-(3-pyridyl)indazole), the process comprising two steps.
  • a reaction mixture solution is formed comprising compound 181a or 181b (2-(chloromethyl)-1-chloro-3-nitro-benzene or 2- (bromomethyl)-1-chloro-3-nitro-benzene), compound 520 (3-aminopyridinium salt), and a solvent system, and the reaction mixture is reacted to form a reaction product mixture comprising compound 182a or 182b (N-[(2-chloro-6-nitro- phenyl)methyl]pyridin-3-amine or N-[(2-bromo-6-nitro-phenyl)methyl]pyridin-3- amine) according to the following reaction scheme.
  • compound 520 is a hydrochloride, hydrobromide, sulfate, bisulfate, methanesulfonate, or p-toluenesulfonate salt. In some such aspects compound 520 optionally is prepared in situ or prepared and isolated prior to use.
  • the solvent system is comprises or predominately comprises a polar aprotic solvent. In some such aspects the solvent system comprises acetonitrile, benzonitrile, sulfolane, or a combination thereof. In some aspects, the solvent system comprises a mixture of a non polar solvent and a polar protic solvent.
  • the solvent system is toluene and water or xylenes and water.
  • a phase transfer catalyst is also included.
  • the PTC is a quaternary ammonium salt.
  • the PTC is tetrabutylammonium bromide.
  • the PTC is used in a catalytic amount.
  • the 182a or 182b product is isolated as the anilinium bromide salt, the di-bromide salt, or a salt mixture of HBr and methanesulfonic acid or p-toluenesulfonic acid.
  • 182a or 182b is treated with a base after the reaction, it is isolated as the free base.
  • a reaction mixture solution is formed comprising 182a or 182b, reductant, a base, and a solvent system, and the reaction mixture is reacted to form a reaction product mixture comprising compound 093a or 093b according to the following reaction scheme [300]
  • the reductant is a reducing agent.
  • the reductant is selected from zinc, iron, or titanium tetrachloride, [301]
  • the base is an inorganic base. In some such aspects the base is a hydroxide base.
  • the base is selected from sodium hydroxide, potassium hydroxide, or cesium hydroxide.
  • titanium tetrachloride is the reductant the base is triethylamine
  • the solvent system is comprised of a mixture of non- polar or polar solvent and a polar protic solvent.
  • the solvent system is selected from water and 1,4-dioxane, water and isopropanol, water and tetrahydrofuran, water and toluene, water and xylenes, water and N- methylpyrrolidone, water and sulfolane, or water and dimethylacetamide
  • the solvent system comprises or predominately comprises a polar protic solvent.
  • the solvent system is water.
  • any of compound 182a, 182b, 093a, or 093b are optionally isolated from the reaction product mixture.
  • any two sequential reactions, or all of the sequential reaction from compound 181a or 181b to 093a or 093b are done in a telescopic pot scheme.
  • Some aspects of the disclosure are directed to an alternate process for the preparation of compound 182a or 182b (N-[(2-chloro-6-nitro- phenyl)methyl]pyridin-3-amine or N-[(2-bromo-6-nitro-phenyl)methyl]pyridin-3- amine).
  • the process comprises forming a reaction mixture comprising compound 003a or 003b (1 (2 chloro 6 nitro phenyl) N (3 pyridyl)methanimine or 1 (2 bromo 6-nitro-phenyl)-N-(3-pyridyl)methanimine), a reducing agent, and a solvent system and reacting the reaction mixture to form a reaction product mixture comprising compound 182a or 182b according to the following reaction scheme.
  • the reducing agent is magnesium.
  • the reducing agent is a borohydride.
  • the reducing agent is selected from sodium borohydride or sodium cyanoborohydride.
  • the solvent system comprises at least one C 1-4 alcohol, a carboxylic acid, or a combination thereof. In some such aspects, the solvent system comprises methanol, ethanol, acetic acid, or a combination thereof. [307] Some aspects of the disclosure are directed to a process for the preparation of compound 093a or 093b (4-chloro-2-(3-pyridyl)indazole or 4-bromo-2- (3-pyridyl)indazole) according to a scheme comprising three steps.
  • Step 1 for preparing compound 093a or 093b comprises forming a reaction mixture comprising compound 114a or 114b (3-chloro-2-methyl-aniline or 3- bromo-2-methyl-aniline), an oxidizing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 115a or 115b (3-chloro-2-methyl-nitrosobenzene or 3-bromo-2-methyl-3-nitroso-benzene) according to the following reaction scheme.
  • the oxidizing agent is potassium peroxymonosulfate, sodium perborate, sodium percarbonate, hydrogen peroxide, peracetic acid, or 3-chloroperbenzoic acid.
  • the solvent system comprises or predominately comprises at least one polar aprotic solvent and at least one polar protic solvent. In some such aspects, the solvent system comprises or predominately comprises dichloromethane and water or dichloroethane and water. [311] In some step 1 aspects, compound 115a or 115b may be optionally isolated from the reaction product mixture.
  • Step 2 for preparing compound 093a or 093b comprises forming a reaction mixture comprising compound 115a or 115b, a source of bromine or a source of chlorine, optionally a radical initiator, and a solvent system, and reacting the reaction mixture under photochemical conditions to form a reaction product mixture comprising compound 116a-d (1-chloro-2-(chloromethyl)-3-nitroso-benzene, 1- chloro-2-(bromomethyl)-3-nitroso-benzene, 1-bromo-2-(chloromethyl)-3-nitroso- benzene, or 1-bromo-2-(bromomethyl)-3-nitroso-benzene) according to the following reaction scheme.
  • the source of Br is N-bromosuccinimide, Br 2 , or HBr and hydrogen peroxide.
  • the source of Cl is N- chlorosuccinimide, trichloroisocyanuric acid, Cl 2 , or HCl and hydrogen peroxide.
  • the photochemical conditions relate to promotion of the reaction using a source of light. In some such step 2 aspects, the photochemical conditions promote the reaction using visible light.
  • a photosensitive or thermally activated radical initiator is used. In some such aspects the radical initiator is azobisisobutyronitrile.
  • the solvent system comprises or predominantly comprises at least one polar aprotic solvent and at least one polar protic solvent. In some such aspects, the solvent system comprises or predominantly comprises dichloromethane and water or dichloroethane and water.
  • compound 116a-d may be optionally isolated from the reaction product mixture.
  • Step 3 of the first scheme for preparing compound 093a or 093b comprises forming a reaction mixture comprising compound 116a-d, compound 520 (3-aminopyridinium salt), and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 093a 093b according to the following reaction scheme.
  • compound 520 is a hydrochloride, hydrobromide, hydroiodide, sulfate, bisulfate, formic, methanesulfonate, or para- toluenesulfonate salt. In some such step 3 aspects, compound 520 is optionally prepared in situ or prepared and isolated prior to use.
  • the solvent system comprises or predominantly comprises a polar aprotic solvent. In some such aspects, the solvent system comprises or predominantly comprises dichloromethane, dichloroethane, or acetonitrile. In some step 3 aspects, the solvent system comprises or predominantly comprises at least one aprotic solvent and at least one polar protic solvent.
  • the solvent system comprises or predominantly comprises dichloromethane and water, dichloroethane and water, acetonitrile and water, toluene and water, or combinations thereof.
  • a phase transfer catalyst is used.
  • the phase transfer catalyst is a quaternary ammonium salt.
  • the phase transfer catalyst is tetrabutylammonium chloride, tetrabutylammonium bromide, or tetrabutylammonium iodide.
  • compound 093a or 093b may be optionally isolated from the reaction product mixture.
  • any of compound 115a or 115 b, 116a-d, or 093 a or 093b are optionally isolated from the reaction product mixture.
  • any two sequential reactions, or all of the sequential reaction from compound 114a or 114b to 093a or 093b are done in a telescopic pot scheme.
  • Some aspects of the disclosure are directed to a first process for the preparation of compound 061 (2-(pyridin-3-yl)-2H-indazole-4-carboxylic acid).
  • the process comprises forming a reaction mixture comprising compound 093a or 93b (4- chloro-2-(3-pyridyl)indazole or 4-bromo-2-(3-pyridyl)indazole), CO, a catalyst, a ligand, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 061 according to the following reaction scheme according to the following reaction scheme [325]
  • the catalyst is selected from a transition metal catalyst, In some aspects, the catalyst is selected from a palladium catalyst, a nickel catalyst, a platinum catalyst, and a copper catalyst. In some aspects, the catalyst is selected from a palladium catalyst.
  • the catalyst is selected from palladium on carbon or palladium acetate.
  • the ligand is a diphosphine ligand.
  • the ligand is 1,3-bis(dicyclohexylphosphium)propane bis(tetrafluoroborate),1,3-bis(dicyclohexylphosphino)propane, 1,3- bis(diphenylphosphino)propane, or 1,3-bis(diphenylphoshonium) bis(tetrafluoroborate).
  • the ligand is 1,3- bis(dicyclohexylphosphino)propane bis(tetrafluoroborate).
  • the base is an inorganic base. In some such aspects, the base is a carbonate. In some such aspects, the base is selected from sodium carbonate, sodium bicarbonate, potassium carbonate, and potassium bicarbonate. In some such aspects, the base is potassium carbonate.
  • the reaction atmosphere comprises or predominately comprises a mixture CO and N 2 . In some aspects, the reaction atmosphere comprises or predominately comprises CO. In some aspects, the reaction temperature is at least 100 °C.
  • the solvent system comprises or predominantly comprises a polar aprotic solvent. In some aspects, the solvent system comprises or predominantly comprises dimethyl sulfoxide. In some aspects, the solvent system further comprises water.
  • the solvent system comprises dimethyl sulfoxide and water.
  • Some aspects of the disclosure are directed to a second process for the preparation of compound 061 (2-(3-pyridyl)indazole-4-carboxylic acid). The process comprises forming a reaction mixture comprising compound 038 (methyl 2-(3- pyridyl)indazole-4-carboxylate), a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 061 according to the following reaction scheme .
  • the base is an alkali metal hydroxide. In some such aspects, the base is potassium hydroxide or sodium hydroxide. In some such aspect, the base is sodium hydroxide.
  • the solvent system comprises or predominantly comprises water and a polar organic solvent.
  • the solvent system comprises or predominantly comprises water and at least one solvent selected from acetone, acetonitrile, isopropanol, methanol, ethanol, dimethylsulfoxide, dimethylacetamide, dimethylformamide, N-methylpyrrolidone, and combinations thereof.
  • Some aspects of the disclosure are directed to a process for the preparation of compound 038 (methyl 2-(3-pyridyl)indazole-4-carboxylate according to a first, second, or third scheme [334]
  • the first scheme for preparing compound 038 comprises three steps.
  • Step 1 of the first scheme for preparing compound 038 comprises forming a reaction mixture comprising compound 400 (methyl 3-amino-2- methylbenzoate), an oxidizing agent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 500 (methyl 2- methyl-3-nitrosobenzoate) according to the following reaction scheme
  • the oxidizing agent is potassium peroxymonosulfate, sodium perborate, sodium percarbonate, hydrogen peroxide, peracetic acid, or 3-chloroperbenzoic acid.
  • the solvent system comprises or predominantly comprises at least one polar aprotic solvent and at least one polar protic solvent.
  • the solvent system comprises or predominantly comprises dichloromethane and water or dichloroethane and water.
  • compound 500 may be optionally isolated from the reaction product mixture.
  • Step 2 of the first scheme for preparing compound 038 comprises forming a reaction mixture comprising compound 500, a source of bromine or a source of chlorine, optionally a radical initiator, and a solvent system, and reacting the reaction mixture under photochemical conditions to form a reaction product mixture comprising compound 510a or 510b (methyl 2-(bromomethyl)-3-nitrosobenzoate or methyl 2-(chloromethyl)-3-nitrosobenzoate) according to the following reaction scheme .
  • the source of Br is N- bromosuccinimide, Br 2 , or HBr and hydrogen peroxide.
  • the source of Cl is N-chlorosuccinimide, trichloroisocyanuric acid, Cl 2, or HCl and hydrogen peroxide.
  • the photochemical conditions relate to promotion of the reaction by a source of light.
  • a photosensitive or thermally activated radical initiator may be used optionally.
  • the radical initiator is azobisisobutyronitrile.
  • the solvent system comprises or predominantly comprises at least one polar aprotic solvent and at least one polar protic solvent. In some such aspects, the solvent system comprises or predominantly comprises dichloromethane and water or dichloroethane and water.
  • compound 510a or 510b may be optionally isolated from the reaction product mixture.
  • Step 3 of the first scheme for preparing compound 038 comprises forming a reaction mixture comprising compound 510a or 510b, compound 520 (3- aminopyridinium salt), and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 038 according to the following reaction scheme. .
  • compound 520 is a hydrochloride, or hydrobromide, hydroiodide, sulfate, bisulfate, methanesulfonate, or p- toluenesulfonate salt.
  • compound 520 is a hydrochloride salt.
  • the compound 520 optionally is prepared in situ or prepared and isolated prior to use.
  • the solvent system comprises or predominantly comprises a polar aprotic solvent. In some such aspects, the solvent system comprises or predominantly comprises dichloromethane, dichloroethane, or acetonitrile.
  • the solvent system comprises or predominantly comprises at least one aprotic solvent and at least one polar protic solvent. In some such aspects, the solvent system comprises or predominantly comprises dichloromethane and water, dichloroethane and water, acetonitrile and water, or toluene and water.
  • a phase transfer catalyst is used. In some such step 3 aspects, the phase transfer catalyst is a quaternary ammonium salt. In some such step 3 aspects, the phase transfer catalyst is tetrabutylammonium chloride or tetrabutylammonium bromide.
  • compound 038 may be optionally isolated from the reaction product mixture.
  • any of compound 500, 510a or 510b, or 038 are optionally isolated from the reaction product mixture.
  • any two sequential reactions, or all of the sequential reaction from compound 400 to 038 are done in a telescopic pot scheme.
  • the second scheme for preparing compound 038 comprises three steps.
  • Step 1 of the second scheme for preparing compound 038 comprises forming a reaction mixture comprising compound 400 where “Protec” refers to an amine protecting group,, a source of bromine or a source of chlorine, and a solvent system, and reacting the reaction mixture by exposure to a source of light to form a reaction product mixture comprising compound 410 (methyl 3-amino-2- (bromomethyl)benzoate or methyl 3-amino-2-(chloromethyl)benzoate) according to the following reaction scheme [354]
  • the source of Br is Br 2 and hydrogen peroxide.
  • the source of Cl is Cl 2.
  • the source of Cl is Cl 2. and hydrogen peroxide.
  • the protected amine is acetamide of the structure - NHC(O)CH 3 .
  • the solvent system comprises or predominantly comprises at least one polar aprotic solvent and at least one polar protic solvent. In some such aspects, the solvent system comprises or predominantly comprises dichloromethane and water.
  • compound 410 may be optionally isolated from the reaction product mixture.
  • the protecting group is removed from compound 400 prior to formation of compound 430 in step 2.
  • Step 2 of the second scheme for preparing compound 038 comprises forming a reaction mixture comprising compound 410, compound 420, an acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 430 ((E)-2-bromo-6-(pyridin-3-yldiazenyl)benzyl acetate or (E)-2-chloro-6-(pyridin-3-yldiazenyl)benzyl acetate) according to the following reaction scheme
  • the acid is an organic acid. In some such aspects, the acid is acetic acid.
  • the solvent system comprises or predominantly comprises acetic acid.
  • compound 430 may be optionally isolated from the reaction product mixture.
  • Step 3 of the second scheme for preparing compound 038 comprises forming a reaction mixture comprising compound 430, a strong acid, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 038 according to the following reaction scheme [364]
  • the strong acid is an inorganic acid. In some such aspects, the acid is a mineral acid. In some such aspects, the acid is HCl.
  • the solvent system comprises or predominantly comprises at least one polar protic solvent. In some such aspects, the solvent system comprises or predominantly comprises water, methanol, ethanol, isopropanol, acetic acid, or a combination thereof.
  • compound 038 may be optionally isolated from the reaction product mixture.
  • the third scheme for preparing 038 (methyl 2-(3-pyridyl)indazole-4- carboxylate) comprises one step.
  • the process comprises forming a reaction mixture comprising compound 093a or 093b (4-chloro-2-(3-pyridyl)indazole or 4-bromo-2- (3-pyridyl)indazole), a catalyst, a ligand, CO, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 038 according to the following reaction scheme.
  • the catalyst is a transition metal catalyst.
  • the catalyst selected from a palladium catalyst, a nickel catalyst, or a copper catalyst.
  • the catalyst is a palladium on carbon or palladium(II) acetate.
  • the ligand is a diphosphine ligand.
  • the ligand is selected from 1,3-bis(dicyclohexylphosphino)propane, 1,3- bis(dicyclohexylphosphonium)propane bis(tetrafluoroborate), 1,3- bis(diphenylphosphino)propane, or 4,5-bis(diphenylphosphino)-9,9- dimethylxanthene.
  • the base is one or more weak inorganic base.
  • the base is a carbonate or phosphate In some such aspects the base is selected from sodium carbonate, sodium bicarbonate, potassium carbonate, potassium bicarbonate, sodium phosphate tribasic, and potassium phosphate tribasic or combinations thereof. In some aspects, the base is an organic base. In some such aspects, the base is triethylamine. [371] In some aspects, the solvent system comprises or predominantly comprises a nonpolar solvent and methanol. In some such aspects, the solvent system comprises or predominantly comprises xylenes and methanol, o-xylene and methanol, or toluene and methanol. In some aspects the solvent system comprises or predominantly comprises a polar aprotic solvent and methanol.
  • the solvent system comprises DMSO and methanol, DMF and methanol, NMP and methanol.
  • the reaction atmosphere is comprised of a mixture of CO and N 2 . In some aspects, the reaction atmosphere is comprised of predominantly CO. In some aspects, the reaction temperature is at least 100°C.
  • the generated compound 038 can be converted in situ to compound 061 (2-(3-pyridyl)indazole-4-carboxylic acid) using hydrolysis under basic or acidic conditions. In some such aspects, the hydrolysis is conducted using alkali metal hydroxide bases. In some such aspects the hydrolysis is conducted using sodium hydroxide or potassium hydroxide.
  • Another aspect of the disclosure is directed to an alternative process for the preparation of compound 038 (methyl 2-(3-pyridyl)indazole-4-carboxylate).
  • the process comprises forming a reaction mixture comprising compound 061 (2-(3- pyridyl)indazole-4-carboxylic acid), an acid, optionally an additive, and a solvent system containing methanol, and reacting the reaction mixture to form a reaction product mixture comprising compound 038 according to the following reaction scheme
  • the acid is an inorganic acid. In some such aspects, the acid is selected from sulfuric acid or hydrochloric acid. In some aspects, the acid is an organic acid. In some such aspects the acid is p-toluene sulphonic acid. [376] In some aspects the additive is a dehydrating agent such as molecular sieves. [377] In some aspects, the solvent system comprises or predominantly comprises a nonpolar solvent and methanol. In some such aspects, the solvent system comprises or predominantly comprises methanol, toluene, hexanes, or combinations thereof.
  • Some aspects of the disclosure are directed to a process for the preparation of compound 092 ((N-(1-methylcyclopropyl)-2-(3-pyridinyl)-2H- indazole-4-carboxamide) by a two-step process.
  • Step 1 for preparing compound 092 (N-(1-methylcyclopropyl)-2-(3- pyridyl)indazole-4-carboxamide) comprises forming a reaction mixture comprising compound 061 (2-(pyridin-3-yl)-2H-indazole-4-carboxylic acid), a chlorinating reagent, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 930 (2-(3-pyridyl)indazole-4-carbonyl chloride) HCl salt according to the following reaction scheme [380]
  • the solvent system comprises or predominantly comprises a nonpolar solvent, a polar aprotic solvent, or a combination thereof.
  • the solvent system comprises or predominantly comprises toluene and N,N-dimethylformamide. In some such aspects, the solvent system comprises or predominantly comprises toluene. In some such aspects, the solvent system comprises or predominantly comprises acetonitrile and N,N-dimethylformamide. In some such aspects, the solvent system comprises or predominantly comprises acetonitrile.
  • the reaction mixture optionally further comprises a catalyst.
  • a suitable catalyst can be selected from among N,N- dimethylformamide, 4-dimethylaminopyridine, triethylamine, N-methyl-2- pyrrolidone, N-methylformanilide, N-formylpyridine, and pyridine.
  • the catalyst is N,N-dimethylformamide. In some such aspects, the catalyst is pyridine.
  • the chlorinating reagent may be selected from thionyl chloride, oxalyl chloride, phosphorous oxychloride, cyanuric chloride, diphosgene, triphosgene , and phosgene. The chlorination reagent is preferably in stoichiometric excess compared to compound 930.
  • compound 930 may be optionally isolated from the reaction product mixture.
  • Step 2 comprises forming a reaction mixture comprising compound 930, compound 070 (1-methylcyclopropanamine), a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 092 according to the following reaction scheme .
  • the solvent system comprises or predominantly comprises a nonpolar solvent, a polar aprotic solvent, or a combination thereof.
  • the solvent system can be selected from among toluene, xylene, N,N-dimethylformamide, N-methyl-2-pyrrolidone, acetonitrile, dimethylacetamide, isopropyl acetate, tetrahydrofuran, dichloromethane, pyridine and sulfolane.
  • the solvent system comprises or predominantly comprises a polar solvent.
  • the solvent system comprises one or more polar solvents.
  • the solvent system comprises or predominantly comprises acetonitrile.
  • the solvent system comprises acetonitrile and N-methyl-2-pyrrolidone.
  • the solvent system comprises or predominantly comprises a nonpolar solvent. In some such aspects, the solvent system comprises or predominantly comprises toluene. In some such aspects, the solvent system comprises toluene and N-methyl-2- pyrrolidone.
  • the base is an inorganic base or an organic base. In some aspects, the organic base can be selected from among triethylamine, N,N-diisopropylethylamine, pyridine, 3-methylpyridine, dimethylaniline, N- methylimidazole, N-methylmorpholine, DABCO and DBU. In some step 2 aspects, the organic base is triethylamine.
  • the organic base is N,N- diisopropylethylamine.
  • the inorganic base can be selected from among sodium carbonate, potassium carbonate, sodium hydroxide, and potassium hydroxide.
  • the process comprises forming a reaction mixture comprising compound 093a or 093b (4-chloro-2-(3-pyridyl)indazole or 4-bromo-2- (3-pyridyl)indazole), compound 070 (1-methylcyclopropanamine), a catalyst, a ligand, CO, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 092 according to the following reaction scheme y , g , O, base ent system 092 .
  • reaction scheme y , g , O base ent system 092 .
  • the catalyst is a transition metal catalyst.
  • the catalyst is selected from palladium catalysts, nickel catalysts, or platinum catalysts.
  • the palladium catalyst is selected from palladium on carbon or palladium(II) acetate.
  • the ligand is a diphosphine ligand.
  • the ligand is selected from 1,3-bis(dicyclohexylphosphino)propane and 1,3- bis(dicyclohexylphosphonium)propane bis(tetrafluoroborate).
  • the base is at least one weak inorganic base.
  • the base is a carbonate or a phosphate.
  • the base is selected from sodium carbonate, sodium bicarbonate, potassium carbonate, cesium carbonate, potassium bicarbonate, sodium phosphate dibasic, sodium phosphate tribasic, potassium phosphate dibasic, and potassium phosphate tribasic or combinations thereof.
  • the base is aluminum hydroxide.
  • the base is an acetate base. In some such aspects, the base is potassium acetate. In some aspects, the base is an alkoxide base. In some such aspects, the base is lithium t-butoxide, sodium t-butoxide, potassium t-butoxide or combinations thereof. In some aspects, the base is an organic base. In some such aspects, the base is a amine base. In some such aspects, the base is selected from among trimethylamine, triethylamine, tributylamine, DBU, DABCO, and N,N- diisopropylethylamine. [392] In some aspects, the solvent system comprises or predominantly comprises a polar aprotic solvent.
  • the solvent system is selected from diglyme, dioxane, acetonitrile, DMF, DMAc, sulfolane, DMSO or some combination thereof. In some such aspects, the solvent system comprises or predominantly comprises dimethylsulfoxide.
  • the reaction atmosphere comprises or predominately comprises a mixture of CO and N 2 . In some aspects, the reaction atmosphere comprises or predominately comprises CO. In some aspects, the reaction temperature is at least 100°C.
  • Some aspects of the disclosure are directed to an alternative process for the preparation of compound 092 (N-(1-methylcyclopropyl)-2-(3-pyridyl)indazole-4- carboxamide).
  • the process comprising forming a reaction mixture comprising compound 061 (2-(3-pyridyl)indazole-4-carboxylic acid), compound 070 (1- methylcyclopropanamine), an activator, a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 092 according to the following reaction scheme [395]
  • the activator is a acyl chloride, an anhydride, an alkyl chloroformate, a sulfonyl chloride, an acyl imidazole, or a triazine chloride.
  • the acyl chloride is selected from acetyl chloride, pivalic chloride, benzoyl chloride, or phosgene.
  • the anhydride is selected from acetic anhydride, pivalic anhydride, or di-tert-butyl dicarbonate.
  • the alkyl chloroformate is selected from methyl chloroformate, ethyl chloroformate, or isobutyryl chloride.
  • the sulfonyl chloride is selected from benzene sulfonyl chloride, p-toluene sulfonyl chloride, or methane sulfonyl chloride.
  • the acyl imidazole is selected from 1,1’- carbonyldiimidazole.
  • the triazine chloride is selected from cyanuric chloride or 2-chloro-4,6-dimethocyl-1,3,5-triazine.
  • the base is an organic base.
  • the base is a tertiary amine base such as triethylamine, diisopropylethylamine, N- methylmorpholine, N-methylpiperidine, diazobicylco[5.4.0]undec-7-ene, tributylamine, or N,N-dimethylbenzylamine.
  • the base is a heterocyclic amine base such as pyridine, 2,6-lutidine, 3-picoline, imidazole, or N- methylimidazole.
  • the solvent system comprises or predominantly comprises at least one nonpolar solvent or polar aprotic solvent. In some such aspects, the solvent system comprises or predominantly comprises acetonitrile, N- methylpyrrolidine, toluene or combinations thereof. In some aspects, the solvent system comprises of predominantly comprises acetonitrile. [398] Some aspects of the disclosure are directed to an alternative process for the preparation of compound 092 (N-(1-methylcyclopropyl)-2-(3-pyridyl)indazole-4- carboxamide).
  • the process comprising forming a reaction mixture comprising compound 038 (methyl 2-(3-pyridyl)indazole-4-carboxylate), compound 070 (1- methylcyclopropanamine), a base, and a solvent system, and reacting the reaction mixture to form a reaction product mixture comprising compound 092 according to the following reaction scheme [399]
  • the base is an organometallic base.
  • the base is selected from organomagnesium bases or organoaluminum bases.
  • the base is an organomagnesium base such as, but not limited to, isopropyl magnesium chloride, isopropyl magnesium bromide, ethyl magnesium chloride, ethyl magnesium bromide, methyl magnesium chloride, or methyl magnesium bromide.
  • the base is an organoaluminum base.
  • the organoaluminum base is a trialkylaluminum base.
  • the base is selected from trimethylaluminum, triethylaluminum, or triisobutylaluminum
  • the base is lithium aluminum hydride [400]
  • the solvent system comprises or predominantly comprises a nonpolar solvent or polar aprotic solvent.
  • the solvent system comprises or predominantly comprises tetrahydrofuran, 2-methyl tetrahydrofuran, 1,4-dioxane, diethylene glycol dimethyl ether, 1,2- dimethyoxyethane, diethyl ether, diisopropyl ether, methyl-tert-butyl ether, or cyclopentylmethyl ether.
  • Some aspects of the disclosure are directed to a process for preparing a compound 092 salt, the process comprising forming a reaction mixture comprising compound 092, a solvent system, an acid, and reacting the reaction mixture to form a reaction product mixture comprising compound 092 salt according to the following reaction scheme [402]
  • the solvent system comprises or predominantly comprises a nonpolar solvent, a polar solvent, or a combination thereof.
  • the acid is an inorganic acid or an organic acid.
  • the inorganic acid can be selected from among hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid and nitric acid.
  • the organic acid can be selected from among acetic acid, glucuronic acid, oxalic acid, malic acid, citric acid, tartaric acid, maleic acid, fumaric acid, succinic acid, benzoic acid, methanesulfonic acid, benzenesulfonic acid, para-toluenesulfonic acid and trifluoroacetic acid.
  • compound 092 may be isolated.
  • compound 092 may be crystallized from a solution thereof in an organic solvent by adding compound 092 seed crystals to the solution of compound 092 followed by charging of water over a period of time and cooling.
  • Crystalline compound 092 may then be isolated by methods known in the art (such as filtration or centrifugation) and optionally washed with water.
  • the isolated crystalline compound 092 may then be optionally dried.
  • step 2 may further comprise the following order of steps: (i) exchanging the solvent system to an organic solvent system suitable for crystallization and form a solution of compound 092 in the organic solvent system; (ii) adding water and optional compound 092 seed crystals thereto to form a slurry; (iii) cooling the slurry; and (iv) isolating crystalline compound 092.
  • the organic solvent is a polar solvent.
  • the polar solvent is selected from water, a ketone, a nitrile, an amide, and a C 1-4 alcohol, and combinations thereof.
  • the polar solvent is selected from water, N-methylpyrrolidone, acetonitrile, dichloromethane, dimethylformamide, dimethylacetamide, dimethylsulfoxide, sulfolane, methylethylketone, ethanol, methanol, propanol, butanol, and isopropanol, and combinations thereof.
  • the solution of compound 092 therein is a concentrated solution but below the saturation point at an elevated temperature of the solvent.
  • Non-limiting examples of some suitable temperatures include, from about 75°C to about 95°C or from about 85°C to about 95°C. However, one skilled in the art will recognize that higher or lower temperature ranges may be suitable depending on the boiling point of the solvent.
  • from about 1% to about 5% of compound 092 seed crystals are added followed by the addition of water over a period of time to form a slurry of crystalline compound 092.
  • the water addition step may be done at approximately the same temperature as the solution of compound 092 in the organic solvent.
  • the volume ratio of water to organic solvent is suitably about 0.5:1, about 0.75:1, about 1:1, about 1.25:1, about 1.5:1, about 2:1, about 2:5:1 or about 3:1, and any range constructed therefrom, such as from about 0.5:1 to about 3:1 or from about 1:1 to about 1.5:1.
  • the addition of water may suitably done over from about 1 hour to about 10 hours, such as about 1 hour, about 2 hours, about 3 hours, about 4 hours, or about 5 hours.
  • the slurry of compound 092 may then be cooled over a period of time to complete compound 092 crystallization.
  • the cooling time is suitably from about 1 hour to about 24 hours, or from about 2 hours to about 12 hours, such as about 3 hours, about 5 hours or about 8 hours.
  • Crystalline compound 092 may then be isolated, washed with water, and dried.
  • the polar solvent is a C 1-4 alcohol, or is ethanol, and crystalline compound 092 is predominantly of Form A.
  • the polar solvent is ACN, and crystalline compound 092 is predominantly of Form B.
  • crystalline compound 092 Form A is characterized by a X-ray powder diffraction pattern generally in accordance with FIG.1.
  • crystalline compound 092 Form B is characterized by a X-ray powder diffraction pattern generally in accordance with FIG.2.
  • Example 1 Compound 223 was methylated with chloromethane to produce compound 775 as follows: CH Cl .
  • a 25 L autoclave was charged with K 2 CO 3 powder (325 mesh, 1.55 kg, 1.2 eq.), potassium iodide (155.4 g, 0.1 eq) and acetone (7.2 L, 6V) at 25-30 °C, followed by addition of ⁇ -acetylbutyrolactone (compound 223) (1.2 kg, 1 eq.).
  • the autoclave vessel was closed and methyl chloride (2 eq) was charged into the autoclave until the pressure reached ⁇ 25 psi.
  • reaction mixture was heated and the temperature maintained at 40-45 °C until ⁇ 2 A% compound 223 remained as monitored by HPLC. After completion of the reaction, the reaction product mixture was cooled to room temperature, filtered and washed with acetone. The filtrate containing crude compound 775 was concentrated under vacuum at 40-45 °C to yield a brown liquid (1.3 kg). HPLC of isolated crude material: compound 223 (non- detect), compound 775 (94.13 A%), O-methylated byproduct (1.01 A%). The yield of compound 775 was 91.2% (93.2 wt%).
  • Example 2 Methylation of compound 223 with chloromethane without addition of KI: Into an autoclave was charged K 2 CO 3 (1.4 eq) and acetone (6V), then ⁇ - acetylbutyrolactone (compound 223, 2 g) was added. Methyl chloride (condensed at - 30 °C, 3 eq) was charged into the autoclave and the autoclave closed. The reaction mass was heated to 55-60 °C and maintained for 18h. The progress of the reaction was monitored by HPLC. After completion of the reaction, the reaction mass was cooled to room temperature, filtered and washed with acetone. The filtrate containing compound 775 was concentrated under vacuum at 40-45 °C.
  • Example 3 Methylation of compound 223 with dimethyl sulfate to produce compound 775: Compound 223 (1 eq.), solvent, dimethyl sulfate (1.2 eq.), base (1.4 eq.), and PTC were charged to a multi-neck round-bottom flask, and stirred for 1h at 25-30° (reactions 6 and 7) or 50-55° (reactions 1-5 and 8-12). The reaction was monitored for completion by HPLC. The results are reported in Table 1, where “ND” refers to not detected, and “NR” refers to not reported.
  • Example 6 [423] Preparation of Compound 200: Into a multi-neck round-bottom flask was charged 9.6% NaOCl (3.5 eq) and the solution was cooled to 10-15 °C. Compound 079 (500 g) was charged slowly into the cooled solution. The reaction was held at room temperature until compound 079 was ⁇ 2 A% by HPLC.
  • the reaction mass was cooled down to 10-15 °C and quenched with aqueous sodium bisulfite ( ⁇ 0.5 eq).
  • the CHCl 3 and aqueous layers were separated, and the aqueous layer washed once with MTBE (5V).
  • the aqueous layer was extracted with DCM (2 x 5V) and the combined DCM layers reduced to 5V by distillation.
  • the solution of compound 200 in DCM was carried forward into the next step.
  • reaction mass was held at 0-5 °C for 2 hours. The reaction mass was then allowed to come to 20-25 °C, held for 2 hours, heated to 40-45 °C and held for 2 hours.
  • Compound 070 was distilled from the reaction mass and collected along with water (290 g, 79.5 wt% by GC, 80.4% yield). Compound 070 was further subjected to fractional distillation with a 1-foot packed column to yield compound 070 with a purity of 95.6 wt% by GC (70.6% yield).
  • Example 9 [432] Example 8 was repeated with ethyl methacrylate. The yield of 2,2- dichloro-1-methylcyclopropyl carboxylic acid was 90%.
  • Example 10 [434] In a dry autoclave reactor, a mixture of t-butanol (100 mL, 1.04 mol), 2,2-dichloro-1-methyl-cyclopropanecarboxylic acid (5 g, 0.029 mol), KOH (11.76 g, 0.17 mol) and 5% Pd/C (1.04 g, 0.0002 mol) was stirred at 130°C under hydrogen (45 bar). The reaction was held for 12-14 hrs.
  • Example 11 Example 10 was repeated but with 2,2-dibromo-1-methyl- cyclopropanecarboxylic acid. A yield of 48% 1-methylcyclopropylcarboxylic acid was achieved.
  • Example 14 In a 2 L 4-neck round-bottom flask, 1-methylcyclopropanecarboxylic acid (48 g, 0.48 mol) and dimethylformamide (1.12 mL, 0.01 mol) were charged into dichloromethane (460 mL, 8.48 mol) under nitrogen atmosphere.
  • reaction mass was cooled to 0-5 °C and thionyl chloride (40 mL, 0.55 mol) was added slowly, maintaining the reaction mass temperature ⁇ 5 °C. After addition was complete, the temperature was raised to 23-25 °C and was held until consumption of starting material was confirmed.
  • methanolic ammonia (268 mL, 1.44 mol) and cooled to 0-5 °C.
  • the acid chloride solution was slowly added to the methanolic ammonia, keeping the temperature between 5-10 °C. After addition was complete, the temperature was brought to 20- 25°C and held for 1 hr. Upon reaction completion, most of the solvent was distilled off.
  • reaction mass was stirred at room temperature and monitored by HPLC. When conversion was complete, the reaction mass was quenched slowly with saturated aqueous NaHCO3 (400 mL, 20V). The reaction mass was extracted with EtOAc (3 x 10V). The combined organic layers were dried over NaSO 4 and concentrated under reduced pressure.1-(1-methylcyclopropyl)ethanone oxime was obtained as a white solid (21.1 g, 95.3 wt%, 92% yield).
  • Example 16 [446] Preparation of N-(1-methylcyclopropyl)acetamide: 1-(1- methylcyclopropyl)ethanone oxime (20.0 g), TsCl,(1.6 g, 0.05 eq.) and MeCN (120 mL, 6V) were charged to a reaction flask and stirred. The reaction mass was heated to 80 °C and reaction progress was monitored by HPLC. Upon complete conversion, the reaction mass was cooled to ambient temperature and activated carbon was charged (1.5 g, 7.5% wt/wt) and stirred for 3 hours. The slurry was filtered through a bed of celite and washed with MeCN (100 mL, 5V).
  • reaction mass was allowed to warm to 25-30 °C and stirred for 1 hour.
  • the reaction was then cooled to 5-10 °C and a solution of potassium sodium tartrate tetrahydrate (8.4 kg dissolved in 32 kg water) was charged into the reaction mass, maintaining the internal temperature ⁇ 20 °C. Once addition was complete, the reaction mass was allowed to warm to 25-30 °C, stirred for 1 hour, then filtered to remove the solids. The filtrate was collected and stored separately. The filter cake was re- charged back into the reactor and re-slurried with a tetrahydrofuran/water solution (10 kg/12 kg). After stirring for 30 minutes, the slurry was filtered. The filtrate was collected and stored separately and the filter cake was subjected to re slurry once more.
  • Example 19 [452] Preparation of 1-methylcyclopropanamine (070): Charged acetonitrile (15 kg), tetrahydrofuran (105.6 kg), and titanium(IV) isopropoxide (119.4 kg) into a jacketed reactor at 25-30 °C and agitated. Cooled the reaction mass to 5-10 °C and charged ethylmagnesium chloride (383.6 kg, 2 M in tetrahydrofuran), maintaining the internal temperature ⁇ 20 °C. After addition was complete, the reaction was allowed to warm to 25-30 °C and stirred for 2 hours. Conversion of acetonitrile was monitored by GC.
  • reaction mass was cooled to 5-10 °C and charged boron trifluoride diethyl etherate (103.7 kg), maintaining the internal temperature ⁇ 20 °C.
  • reaction mass was allowed to warm to 25-30 °C and stirred for 1 hour.
  • the reaction was then cooled to 5-10 °C and a solution of potassium sodium tartrate tetrahydrate (63 kg dissolved in 240 kg water) was charged into the reaction mass, maintaining the internal temperature ⁇ 20 °C.
  • the reaction mass was allowed to warm to 25-30 °C, stirred for 1 hour, then the organic solvent removed by distillation. Partway through the distillation, 300 kg water was charged into the reaction mass.
  • reaction mass was cooled to 5-10 °C and the pH of the reaction mass was adjusted with 50% aqueous sodium hydroxide (138.6 kg) to pH ⁇ 12. After stirring the reaction mass for a period of time, compound 070 was isolated by distillation, along with water (fraction 1 – 40.6 kg, 34.6 wt%; fraction 2 – 88.6 kg, 1.3 wt%; 58.7% yield).
  • the reaction was sampled periodically for IPC analysis by HPLC until compound 339 was ⁇ 1% by area.
  • the reaction was cooled to room temperature and quenched with 4 V of a 10% solution of sodium sulfite in water.
  • the aqueous layer was separated, and the DCM layer was washed with an additional 4 V of water.
  • the aqueous layer was separated, combined with the first aqueous layer, and extracted with 2 V DCM. All of the organic layers were combined and washed with 4 V of a 5% sodium sulfite solution.
  • the organic layer was separated again and washed with 4 V of a saturated sodium chloride solution.
  • the organic layer was separated and distilled to 1 V.
  • the reaction mixture was cooled to 50 °C, and the acetonitrile was distilled until its content was ⁇ 5% by area according to analysis by gas chromatography.
  • the reaction mass was cooled to 25-30 °C, and 500 mL toluene were added.
  • the mixture was stirred for 20 min at this temperature before the layers were allowed to separate.
  • the toluene layer was kept aside, and the aqueous layer was charged back into the reactor, where it was extracted with another 250 mL of toluene. Both toluene layers were combined and washed with 212 mL water.
  • the toluene solution containing (2-chloro-6-nitrophenyl)methanol (compound 050) was taken onto the next step.
  • a 5% aqueous solution of sodium thiosulfate was prepared by dissolving 10.55 g Na 2 S 2 O 3 in 212 mL water. This solution was added to the reaction mass, which was stirred for an additional 25-30 min at room temperature, at which time the layers were separated. The toluene layer was washed with water (2 x 212 mL), and the toluene solution containing 2-chloro-6-nitro benzaldehyde (compound 378) was taken onto the next step. [461] Under nitrogen, the toluene layer containing compound 378 was charged to the reactor along with 3-aminopyridine (98.8 g) and p-toluenesulfonic acid (0.095 g).
  • reaction mass was heated to 105-110 °C; the slurry became a dark homogeneous solution as the temperature was increased.
  • the reaction was stirred at this temperature for 12-16 h with azeotropic distillation of water until compound 378 was no more than 2% by area according to HPLC analysis.
  • the reaction mixture was cooled to room temperature, and the toluene solution of 1-(2- chloro-6-nitrophenyl)-N-(pyridine-3-yl)methanimine (compound 003a) was taken onto the next step.
  • Triethylphosphite (670.9 g) was added to the toluene solution of compound 003a at 25-30 °C under nitrogen.
  • reaction mixture was heated to 105-110 °C for 20-25 h or until compound 003a was no more than 2% by area according to HPLC analysis. At this time, the temperature was reduced to 45-50 °C, and toluene was distilled under 50 mbar vacuum until it was ⁇ 5% by area percent according to GC analysis.
  • the reaction mass was cooled to 25-30 °C, and 92.7 mL of isopropanol was added. The slurry was stirred for 30 min prior to addition of 1110 mL of water. The reaction mass was then cooled to 10-15 °C and stirred for 2 h. The resulting solid was isolated via filtration and washed with 277.5 mL water.
  • Example 21 [465] The above procedure was repeated using compound 093b (4-bromo-2- (3-pyridyl)indazole). Analysis by UHPLC indicated the following area percent for the reaction mixture: compound 061 (2-(3-pyridyl)indazole-4-carboxylic acid) (93.5%), compound 093b (0.3%).
  • HPLC area percent analysis at a wavelength of 220 nm indicated the following reactant and product distribution: 21.5% compound 520a, 14.6% 2- (bromomethyl)-1-chloro-3-nitrobenzene (compound 182a), 47.2 percent of the protonated salt of the desired product N-[(2-chloro-6-nitrophenyl)methyl]pyridine-3- amine, 11.1% of 2-chloro-6-nitrophenyl)methanol (compound 050), and 3.7% of compound 181a.
  • Compound 182a 0.1 g 0.38 mmol
  • zinc dust (0.100 g, 1.52 mmol
  • Tetrahydrofuran (2 mL) was added, and the gray suspension was stirred at room temperature. Shortly after stirring was initiated, NaOH (0.152 g, 3.80 mmol) in 2 mL water was added dropwise, and the reaction was allowed to stir at room temperature for 4h. The organic layer was sampled and analyzed by HPLC, indicating compound 093a had formed in 71 area % along with 29% of N-[(2-chloro- 6-aminophenyl)methyl]pyridine-3-amine.
  • Example 25 Screening of 3-aminopyridine salts (compound 520) for the synthesis of compound 182 [487]
  • Compound 181a (1.0 eq.)
  • the appropriate 3-aminopyridine • HA salt (compound 520) (1.5 eq)
  • solvent was charged to a round bottom flask. The reaction mass was then heated to the listed temperature and were monitored by HPLC analysis for conversion.
  • Example 28 Preparation of methyl 2-(pyridin-3-yl)-2H-indazole-4-carboxylate (compound 038) [499] The procedure from Example 27 was repeated starting from compound 400 (methyl 3-amino-2-methylbenzoate) to prepare compound 038 giving a dichloroethane solution of compound 038 (20.0 A% by HPLC).
  • the reactor was then purged with nitrogen via pressurizing up to three bar and releasing three times. This was followed by injection of DMSO (50 mL), compound 070 (1- methylcyclopropanamine) (7.8 mL, 86.4 mmol) and pentane (48 mL). The reactor was heated to 60 C, and a vent line was opened in an attempt to purge the pentane/water azeotrope. The reactor system was closed and purged again with nitrogen three times followed by a carbon monoxide purge. The reactor was then pressurized up to ⁇ 100- 120 psi with carbon monoxide and heated to 110 degrees C with agitation at 200 rpm.
  • Example 31 [506] Preparation of N-(1-methylcyclopropyl)-2-(3-pyridyl)indazole-4- carboxamide (compound 092) [507] Into a 600 mL Parr pressure reactor at room temperature were charged compound 093a (4-chloro-2-(3-pyridyl)indazole) (41.35 g, 180.0 mmol), 1,3-bis(cyclohexylphosphino)propane tetrafluoroborate (0.661 g, 1.08 mmol), potassium phosphate tribasic (43.96 g, 207.05 mmol), and Pd/C dry (0.575 g, 0.30 mol%).
  • compound 093a (4-chloro-2-(3-pyridyl)indazole) (41.35 g, 180.0 mmol)
  • 1,3-bis(cyclohexylphosphino)propane tetrafluoroborate
  • the reactor was then purged with nitrogen via pressurizing up to three bar and releasing three times. This was followed by injection of DMSO (300 mL) and compound 070 (13.44 g, 189.04 mmol). The reactor was then pressurized up to 75 psi with carbon monoxide and heated to 110 ° C with agitation at 200 rpm. Agitation continued under these conditions for 8 h, then the reactor was cooled to room temperature and purged with nitrogen for IPC sampling.
  • Example 33 Effect of CO Partial Pressure on the Rate of Consumption of Compound 093 in the Aminocarbonylation Reaction to Form Compound 092
  • Compound 093 (5.74 g, 1.0 eq), Pd (0.3 mol%) charged as 10 wt% Pd on Carbon, 1,3-bis(cyclohexylphosphino)propane tetrafluoroborate (Ligand:Pd 2:1), H 3 PO 4 base (1.2 eq.), compound 070 (1.5 eq.), and DMSO (7.3V) were charged into a reactor that was purged with nitrogen,purged with CO, then pressurized with CO to the desired pressure .
  • reaction mass was then heated to 110 °C and agitated for 20 hr.
  • the CO gas uptake was measured to determine the rate and conversion of each reaction as a function of time.
  • the amount of CO consumed and reaction conversion at 5.1 hr is shown for each reaction in Table 5.
  • the final reaction mass at 20 hr was then analyzed using HPLC Area% analysis, and the results are reported in Table 6. The data show that reaction selectivity is approximately the same at full conversion regardless of CO pressure or rate. [517] Table 5.
  • CO Consumed and Reaction Conversion at 5.1 hr [518] Table 6.
  • the reactor was then purged with nitrogen via pressurizing up to three bar and releasing three times. This was followed by injection of xylenes (36.4 mL) and methanol (8.5 mL). The reactor system was closed and purged again with nitrogen three times followed by a carbon monoxide purge. The reactor was then pressurized up to ⁇ 60 psi with carbon monoxide and heated to 140 degrees C with agitation at 800 rpm. The gauge pressure was ⁇ 75 psi. Agitation continued under these conditions for 20 h, then the reactor was cooled to room temperature and purged with nitrogen for IPC sampling.
  • Example 38 [532] Preparation of N-(1-methylcyclopropyl)-2-(3-pyridinyl)-2H-indazole 4-carboxamide (compound 092) [533] Charged methyl 2-(pyridin-3-yl)-2H-indazole-4-carboxylate (compound 038) (200 mg), THF (10 V), and 1-methylcyclopropaneamine (compound 070) (2.5 eq.) to a dry flask with stirring under nitrogen. The reaction mass was cooled to 0 °C.
  • isopropyl magnesium chloride (2.0 eq.) was charged slowly over 5 min, keeping the reaction temperature below 10 °C. The reaction was then held at 0 °C for 4 hrs. Then water (5 V) was added slowly over 5 minutes after which additional water (15 V) was added and the reaction mass was stirred at 23 °C for 10 min. The slurry was filtered and washed with water (3 x 15 V).
  • Part B Charged the acid chloride from Part A, acetonitrile (14V), and N-methylpyrrolidone (1V) into a jacketed reactor with stirring under nitrogen. Then charged 1-methylcyclopropanamine (1.2 eq.) (compound 070) slowly into the reaction mass. Lastly, charged triethylamine (2.1 eq.) slowly into the reaction mass, maintaining the temperature ⁇ 40 °C.
  • reaction mass was heated to 60-65 °C and held until HPLC indicated completion of the reaction to compound 092.
  • Acetonitrile was distilled off at ⁇ 50 °C to ⁇ 3V under vacuum.
  • the reaction mass was cooled to room temperature and N-methylpyrrolidone (2V) was charged.
  • the reaction mass was heated to 95-100 °C and held for 10 mins, cooled to 90 °C and held for 15 mins, then 3 wt% N-(1-methylcyclopropyl)-2-(3-pyridinyl)-2H-indazole 4-carboxamide (compound 092) seed was charged. Water (2.5V) was charged at 90 °C over 3 hours.
  • reaction mass was cooled to 40-45 °C and N- methylpyrrolidone (1V) was charged.
  • the reaction mass was distilled to remove most of the remaining toluene.
  • the reaction mass was then cooled to 25-30 °C and acetonitrile (14V) was charged, followed by slow addition of 1- methylcyclopropanamine (1.2 eq.) (compound 070) into the reaction mass.
  • triethylamine (2 eq.) was charged slowly into the reaction mass.
  • the reaction mass was heated to 60-65 °C and held until HPLC indicated completion of the reaction to compound 092.
  • Acetonitrile was distilled off at ⁇ 50 °C to ⁇ 3V under vacuum.
  • the reaction mass was cooled to 25-30 °C.
  • Example 42 [547] Preparation and Analysis of the Crystalline Compound 092 Form A by single-crystal X-ray diffraction [548] Solids of compound 092 (109.1 mg) were combined with EtOH (4 mL) with stirring at about 72°C, and the resulting slurry was left to stir at about 72- 73°C. After about 1 day, the bulk of solids in the sample were isolated by positive- pressure filtration. Some solids remained in the original vial following filtration, and from these a single crystal was culled and analyzed. A colorless needle having approximate dimensions of 0.55 ⁇ 0.04 ⁇ 0.03 mm 3 , was mounted on a polymer loop in random orientation.
  • Example 43 [551] Preparation and Analysis of the Crystalline Compound 092 Form B by single-crystal X-ray diffraction [552] Solids of compound 092 (102.6 mg) were combined with ACN (4 mL) with stirring at about 72-73°C, and the resulting slurry was left to stir at about 72-73°C. After 1 day, the solids in the sample were isolated by positive-pressure filtration, and the warm filtrate was placed directly on the lab bench to cool to RT. After standing at RT for 6 days, a clear liquid and white solids consisting of spherulites of thin needles were observed. A needle was culled and analyzed.
  • Form B is an anhydrous/non-solvated form of compound 092.
  • the crystal data and data collection parameters for compound 092 Form B are shown in the table 9. [553] Table 9.
  • Example 44 [555] X-Ray Powder Diffraction characterization of Compound 092 for polymorphs form identification [556] Powder X-ray diffraction was used to identify the crystalline phases of various samples of Compound 092. X-ray diffraction patterns were collected with a PANalytical X'Pert PRO MPD or a PANalytical Empyrean diffractometer using an incident beam of Cu radiation produced using an Optix long, fine-focus source. An elliptically graded multilayer mirror was used to focus Cu K ⁇ X-rays through the specimen and onto the detector.
  • a silicon specimen (NIST SRM 640e) was analyzed to verify the observed position of the Si 111 peak is consistent with the NIST-certified position.
  • a specimen of the sample was sandwiched between 3- ⁇ m-thick films and analyzed in transmission geometry.
  • a beam-stop, short antiscatter extension, and antiscatter knife edge were used to minimize the background generated by air.
  • Soller slits for the incident and diffracted beams were used to minimize broadening from axial divergence.
  • Diffraction patterns were collected using a scanning position-sensitive detector (X'Celerator) located 240 mm from the specimen and Data Collector software v.5.5. [557] Diffraction maxima were identified from the X-ray diffractograms generated by the software.
  • a characteristic subset of the 2 ⁇ diffraction maxima for polymorph A of Compound 092 is given in Table 1.
  • a characteristic subset of the 2 ⁇ diffraction maxima for polymorph B of Compound 092 is given in Table 2.
  • the polymorph form of a sample of unknown polymorph form could be easily determined by comparing its characteristic 2 ⁇ X-ray maxima to the characteristic 2 ⁇ maxima shown in Tables 1 and 2, respectively.
  • the X-ray powder diffraction (XRPD) diagram for compound 092 Form A is shown in FIG.1.
  • the XRPD diagram for compound 092 Form B is shown in FIG.2.
  • Example 46 Compound 092 Form A and Form B Interconversion Study [565] Relative thermodynamic stabilities of anhydrous/non-solvated Forms A and B were studied at 2-8°C, room temperature (RT) and at 71-72°C via interconversion (competitive) slurries. In these slurries, a given solvent system was pre-saturated with compound 092 (Form A + minor Form B) at the stated temperature, and a portion of the liquid phase was filtered into a mixture of solids containing relatively equal amounts of Form A and Form B.
  • the word “predominantly” means greater than 50%, at least 75%, at least 90%, at least 95%, or at least 99% on a relevant basis such as, for instance and without limitation, population%, w/w%, w/v%, v/v%, and area%.

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AR128557A1 (es) 2024-05-22
CN118679154A (zh) 2024-09-20

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