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【结 构 式】 
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【分子编号】34654 【品名】ethyl 1-cyclopropyl-7-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylate 【CA登记号】 |
【 分 子 式 】C16H16FNO4 【 分 子 量 】305.3057832 【元素组成】C 62.95% H 5.28% F 6.22% N 4.59% O 20.96% |
合成路线1
该中间体在本合成路线中的序号：(X)Aromatic hydroxylation of 1-bromo-2,4-difluorobenzene (I) using tert-butyl hydroperoxide and LDA afforded phenol (II), which was methylated with iodomethane and K2CO3 to give methyl ether (III). The required benzoic acid (IV) was then obtained from (III) by lithium-bromine exchange with n-butyllithium, followed by carboxylation with CO2 gas at -70 C. Treatment of (IV) with oxalyl chloride and DMF gave acid chloride (V). This was condensed with the lithium salt of monoethyl malonate to yield, after acid decarboxylation, ketoester (VI). Subsequent condensation of (VI) with triethyl orthoformate in refluxing Ac2O provided methoxyacrylate (VII), and further treatment with cyclopropylamine (VIII) furnished aminoacrylate (IX). Cyclization of (IX) by means of NaH in THF generated the quinolone system (X). Acid hydrolysis of the ethyl ester group of (X) gave quinolinecarboxylic acid (XI), which was converted to the boron difluoride complex (XII) by treatment with BF3-Et2O in hot THF. Displacement of the aromatic fluorine of (XII) with 3R-(1S-tert-butoxycarbonylaminoethyl)pyrrolidine (XIII) in the presence of DIEA, followed by boron complex cleavage with Et3N in EtOH provided the pyrrolidinylquinoline (XIV). Finally, the Boc protecting group of (XIV) was removed by hydrolysis with ethanolic HCl.
| 【1】 Hu, X.E.; Gray, J.L.; Almstead, J.-I.K.; Ledoussal, B. (The Procter & Gamble Co.); Antimicrobial quinolones, their compsns. and uses. EP 1015445; WO 9914214 . |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| 15086 | 3-ethoxy-3-oxopropionic acid | 1071-46-1 | C5H8O4 | 详情 | 详情 | |
| (I) | 15488 | 1-bromo-2,4-difluorobenzene | 348-57-2 | C6H3BrF2 | 详情 | 详情 |
| (II) | 34648 | 3-bromo-2,6-difluorophenol | 221220-99-1 | C6H3BrF2O | 详情 | 详情 |
| (III) | 34649 | 3-bromo-2,6-difluorophenyl methyl ether; 1-bromo-2,4-difluoro-3-methoxybenzene | 221221-00-7 | C7H5BrF2O | 详情 | 详情 |
| (IV) | 30621 | 2,4-difluoro-3-methoxybenzoic acid | 178974-97-5 | C8H6F2O3 | 详情 | 详情 |
| (V) | 34650 | 2,4-difluoro-3-methoxybenzoyl chloride | C8H5ClF2O2 | 详情 | 详情 | |
| (VI) | 34651 | ethyl 3-(2,4-difluoro-3-methoxyphenyl)-3-oxopropanoate | C12H12F2O4 | 详情 | 详情 | |
| (VII) | 34652 | ethyl (Z)-2-(2,4-difluoro-3-methoxybenzoyl)-3-ethoxy-2-propenoate | C15H16F2O5 | 详情 | 详情 | |
| (VIII) | 12263 | Cyclopropylamine; Cyclopropanamine | 765-30-0 | C3H7N | 详情 | 详情 |
| (IX) | 34653 | ethyl (Z)-3-(cyclopropylamino)-2-(2,4-difluoro-3-methoxybenzoyl)-2-propenoate | C16H17F2NO4 | 详情 | 详情 | |
| (X) | 34654 | ethyl 1-cyclopropyl-7-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylate | C16H16FNO4 | 详情 | 详情 | |
| (XI) | 34655 | 1-cyclopropyl-7-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid | 221221-16-5 | C14H12FNO4 | 详情 | 详情 |
| (XII) | 34656 | C14H11BF3NO4 | 详情 | 详情 | ||
| (XIII) | 34657 | tert-butyl (1S)-1-[(3R)pyrrolidinyl]ethylcarbamate | C11H22N2O2 | 详情 | 详情 | |
| (XIV) | 34658 | 7-((3R)-3-[(1S)-1-[(tert-butoxycarbonyl)amino]ethyl]pyrrolidinyl)-1-cyclopropyl-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid | C25H33N3O6 | 详情 | 详情 |
合成路线2
该中间体在本合成路线中的序号：(X)Metalation of 1-bromo-2,4-difluorobenzene (I) by means of LDA, followed by treatment with tert-butyl hydroperoxide gave rise to phenol (II), which was further converted to methyl ether (III) by alkylation with iodomethane and K2CO3. Lithium halogen exchange of (III) with n-butyllithium, and subsequent quenching with CO2 produced 3-methoxy-2,4-difluorobenzoic acid (IV). After activation of (IV) as the acid chloride (V), condensation with the lithium derivative of monoethyl malonate (A) led to the benzoyl acetate ester (VI). The benzoyl ethoxyacrylate (VII), obtained by condensation of ketoester (VI) with triethyl orthoformate, was then reacted with cyclopropylamine (VIII) to afford enamine (IX). This was cyclized to the quinolone compound (X) upon treatment with NaH in THF. Acidic hydrolysis of ester (X) gave a keto acid, which was subsequently converted to the boron chelate (XI) by treatment with boron trifluoride etherate. Fluoride displacement of quinolone (XI) with the amino piperidine (XII) produced the piperidino quinolone (XIII). The boron difluoride complex of (XIII) was finally removed by means of triethylamine in boiling EtOH.
| 【1】 Hu, X.E.; Gray, J.L.; Almstead, J.-I.K.; Ledoussal, B. (The Procter & Gamble Co.); Antimicrobial quinolones, their compsns. and uses. EP 1015445; WO 9914214 . |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (A) | 15086 | 3-ethoxy-3-oxopropionic acid | 1071-46-1 | C5H8O4 | 详情 | 详情 |
| (I) | 15488 | 1-bromo-2,4-difluorobenzene | 348-57-2 | C6H3BrF2 | 详情 | 详情 |
| (II) | 34648 | 3-bromo-2,6-difluorophenol | 221220-99-1 | C6H3BrF2O | 详情 | 详情 |
| (III) | 34649 | 3-bromo-2,6-difluorophenyl methyl ether; 1-bromo-2,4-difluoro-3-methoxybenzene | 221221-00-7 | C7H5BrF2O | 详情 | 详情 |
| (IV) | 30621 | 2,4-difluoro-3-methoxybenzoic acid | 178974-97-5 | C8H6F2O3 | 详情 | 详情 |
| (V) | 34650 | 2,4-difluoro-3-methoxybenzoyl chloride | C8H5ClF2O2 | 详情 | 详情 | |
| (VI) | 34651 | ethyl 3-(2,4-difluoro-3-methoxyphenyl)-3-oxopropanoate | C12H12F2O4 | 详情 | 详情 | |
| (VII) | 34652 | ethyl (Z)-2-(2,4-difluoro-3-methoxybenzoyl)-3-ethoxy-2-propenoate | C15H16F2O5 | 详情 | 详情 | |
| (VIII) | 12263 | Cyclopropylamine; Cyclopropanamine | 765-30-0 | C3H7N | 详情 | 详情 |
| (IX) | 34653 | ethyl (Z)-3-(cyclopropylamino)-2-(2,4-difluoro-3-methoxybenzoyl)-2-propenoate | C16H17F2NO4 | 详情 | 详情 | |
| (X) | 34654 | ethyl 1-cyclopropyl-7-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylate | C16H16FNO4 | 详情 | 详情 | |
| (XI) | 59792 | 1-cyclopropyl-3-{[(difluoroboryl)oxy]carbonyl}-7-fluoro-8-methoxy-4(1H)-quinolinone | C14H11BF3NO4 | 详情 | 详情 | |
| (XII) | 59793 | (3S,4R)-4-ethyl-3-piperidinamine; (3S,4R)-4-ethylpiperidinylamine | C7H16N2 | 详情 | 详情 | |
| (XIII) | 59794 | 7-[(3S,4R)-3-amino-4-ethylpiperidinyl]-1-cyclopropyl-3-{[(difluoroboryl)oxy]carbonyl}-8-methoxy-4(1H)-quinolinone | C21H26BF2N3O4 | 详情 | 详情 |
合成路线3
该中间体在本合成路线中的序号：(XXI)The intermediate quinolone boron chelate (X) is prepared as follows. Ketalization of 2’,4’-difluoroacetophenone (XII) with ethylene glycol and p-TsOH provides compound (XIII), which is hydroxylated to phenol (XIV) by ortho-metalation with BuLi in THF at –65 °C, followed by treatment with trimethyl borate in AcOH and then with aqueous H2O2. Acidic hydrolysis of the ethylene ketal moiety of compound (XIV) provides the hydroxyketone (XV), which is alkylated with dimethyl sulfate and K2CO3 in toluene to give 2’,4’-difluoro-3’-methoxyacetophenone (XVI). Carboxylation of acetophenone (XVI) with diethyl carbonate and NaH gives the 2-(benzoyl)acetate (XVII), which is further condensed with dimethylformamide dimethyl acetal (DMFDMA) to produce adduct (XVIII). Subsequent displacement of the dimethylamino group of (XVIII) with cyclopropylamine (XIX) in hot toluene furnishes the N-cyclopropyl analogue (XX) (1, 2). Then, cyclization of (XX) by means of either NaH in THF or N,O-bis(trimethylsilyl)acetamide (BSA) in boiling toluene yields the quinolone carboxylate (XXI), which is hydrolyzed to the corresponding carboxylic acid (XXII) under acidic conditions. Finally, the boron chelate (X) is obtained by complexation of the keto acid (XXII) with the reagent generated from boron oxide and acetic anhydride in AcOH (1-3). Scheme 2.
| 【1】 Reilly, M. (The Procter & Gamble Co.). A coupling process for preparing quinolone intermediates. CA 2647454, EP 1999125, US 2007232804, US 7456279, WO 2007110835. |
| 【2】 Hayes, M.P., Schunk, T.T. (The Procter & Gamble Co.). A hydride reduction process for preparing quinolone intermediates. CA 2647457, EP 1999106, US 2007232806, WO 2007110836. |
| 【3】 Ledoussal, B., Hu, X.E., Gray, J.L., Almstead, J.-I.K. (The Procter & Gamble Co.). Antimicrobial quinolones, their compositions and uses. CA 2303389, EP 1015445, JP 2001516756, US 6329391, US 6387928, WO 1999014214. |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (X) | 65888 | C18H17BFNO6 | 详情 | 详情 | ||
| (XII) | 65890 | 2',4'-Difluoroacetophenone; 1-(2,4-Difluorophenyl)ethanone | 364-83-0 | C8H6F2O | 详情 | 详情 |
| (XIII) | 65891 | 2-(2,4-difluorophenyl)-2-methyl-1,3-dioxolane | C10H10F2O2 | 详情 | 详情 | |
| (XIV) | 65892 | 2-(2,4-difluoro-3-hydroxyphenyl)-2-methyl-1,3-dioxolane | C10H10F2O3 | 详情 | 详情 | |
| (XV) | 65893 | 2',4'-Difluoro-3'-hydroxyacetophenone; 1-(2,4-Difluoro-3-hydroxyphenyl)ethanone | 951163-65-8 | C8H6F2O2 | 详情 | 详情 |
| (XVI) | 65894 | 2',4'-Difluoro-3'-methoxyacetophenone; 1-(2,4-Difluoro-3-methoxyphenyl)ethanone | 373603-19-1 | C9H8F2O2 | 详情 | 详情 |
| (XVII) | 34651 | ethyl 3-(2,4-difluoro-3-methoxyphenyl)-3-oxopropanoate | C12H12F2O4 | 详情 | 详情 | |
| (XVIII) | 65895 | C15H17F2NO4 | 详情 | 详情 | ||
| (XIX) | 12263 | Cyclopropylamine; Cyclopropanamine | 765-30-0 | C3H7N | 详情 | 详情 |
| (XX) | 34653 | ethyl (Z)-3-(cyclopropylamino)-2-(2,4-difluoro-3-methoxybenzoyl)-2-propenoate | C16H17F2NO4 | 详情 | 详情 | |
| (XXI) | 34654 | ethyl 1-cyclopropyl-7-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylate | C16H16FNO4 | 详情 | 详情 | |
| (XXII) | 34655 | 1-cyclopropyl-7-fluoro-8-methoxy-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid | 221221-16-5 | C14H12FNO4 | 详情 | 详情 |