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HRID 1826535생성일: 2026년 10월 26일

Triethylamine → 1-{2-[6-chloro-8-(3-fluorophenyl)-9-methyl-9H-2-purinyl]-1-ethynyl}-1-cyclopentanol

https://huagongshe.com/reaction/1826535

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-EthynylcyclopentanolHCID 87074—
반응물6-chloro-8-(3-fluorophenyl)-2-iodo-9-methyl-9H-purineHCID 9952265—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-{2-[6-chloro-8-(3-fluorophenyl)-9-methyl-9H-2-purinyl]-1-ethynyl}-1-cyclopentanolHCID 1057123588%

반응 단계

6-Chloro-8-(3-fluorophenyl)-2-iodo-9-methyl-9H-purine (1076 g) was dissolved in 10 liters of tetrahydrofuran and 97.2 g of bistriphenylphosphine palladium dichloride, 26.4 g of cuprous iodide and 248 g of 1-ethynylcyclopentanol were added thereto. Into this mixture were added dropwise 331 ml of triethylamine within 15 minutes keeping the bulk temperature at not higher than 26° C. in a nitrogen atmosphere. After reacting at room temperature for 4 hours, the reaction solution was diluted with 10 liters of ethyl acetate and washed with 4 liters of a saturated ammonium chloride solution and 1 liter of brine. The organic layer was dried over 2 kg of anhydrous sodium sulfate and filtered followed by concentrating to an extent of 3 liters. The resulting residue was diluted with 4 liters of hexane-ethyl acetate (1:1), filtered and washed with 1 liter of hexane to give 732 g of 1-{2-[6-chloro-8-(3-fluorophenyl)-9-methyl-9H-2-purinyl]-1-ethynyl}-1-cyclopentanol. The yield was 88%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE039112E1
출처 데이터셋uspto-grants-2006_05
ORD IDord-ecd5df25507d4e96a9a920cc40122106
출처 메모uspto-grants-2006_05