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HRID 879354作成日:2026年10月25日

Lithium Chloride → (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(1-methyl-1H-pyrazolo[4,3-b]pyridin-5-yl)pyridin-4-yl)benzo[d]thiazol-6-yl)acetate

https://huagongshe.com/reaction/879354

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium ChlorideHCID 433294—
反応物(S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(2-chloropyridin-4-yl)-5-methylbenzo[d]thiazol-6-yl)acetateHCID 86700142—
反応物1-methyl-5-(tributylstannyl)-1H-pyrazolo[4,3-b]pyridineHCID 86700155—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418397HCID 178418397—
生成物(S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(2-(1-methyl-1H-pyrazolo[4,3-b]pyridin-5-yl)pyridin-4-yl)benzo[d]thiazol-6-yl)acetateHCID 86700154—

反応条件

温度120 °C

反応手順

To a solution of (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-2-(2-chloropyridin-4-yl)-5-methylbenzo[d]thiazol-6-yl)acetate (48 mg, 0.091 mmol) in microwave vial, was added 1-methyl-5-(tributylstannyl)-1H-pyrazolo[4,3-b]pyridine (47 mg, 0.111 mmol), copper(I) iodide (9 mg, 0.045 mmol), lithium chloride (11 mg, 0.27 mmol), Pd(PPh3)4 (10 mg, 0.009 mmol). The reaction mixture was heated at 120° C. for 4 hours. Then the mixture was washed by saturated NaHCO3, extracted by EtOAc, the organic phase was dried over MgSO4, filtered, concentrated down, purified by silica gel column, eluting by 0-60% EtOAc in hexanes to give the product. LCMS-ESI+: calc'd for C34H32ClN5O3S: 626.2 (M+H+); found: 626.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08987250B2
出典データセットuspto-grants-2015_03
ORD IDord-eec5377f94c244d6babdc0ab779651a7
出典メモuspto-grants-2015_03