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HRID 879519作成日:2026年10月26日

Potassium Carbonate → (S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(1-methyl-1H-benzo[d]imidazol-6-yl)benzo[d]thiazol-6-yl)acetate

https://huagongshe.com/reaction/879519

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1-Methyl-1H-benzoimidazole-6-boronic acidHCID 46738679—
反応物(S)-ethyl 2-(2-bromo-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetateHCID 86700141—
触媒HCID 178418397HCID 178418397—
溶媒Ethyl AcetateHCID 8857—
生成物(S)-ethyl 2-tert-butoxy-2-(7-(4-chlorophenyl)-5-methyl-2-(1-methyl-1H-benzo[d]imidazol-6-yl)benzo[d]thiazol-6-yl)acetateHCID 86700339—

反応条件

温度100 °C

反応手順

A microwave vial was charged with (S)-ethyl 2-(2-bromo-7-(4-chlorophenyl)-5-methylbenzo[d]thiazol-6-yl)-2-tert-butoxyacetate (75 mg, 0.15 mmol), 1-methyl-1H-benzo[d]imidazol-6-ylboronic acid (34 mg, 0.19 mmol), then Pd(PPh3)4 (34 mg, 0.03 mmol). The vial was flushed with argon, diluted with dioxane (1.5 mL) and to this was added 2M aqueous K2CO3 (0.25 mL, 0.50 mmol). The vial was sealed, heated to 100° C. for 2 hours, and then allowed to cool to room temperature. The mixture was diluted with EtOAc, dried over Na2SO4, filtered, and concentrated in vacuo. The crude residue was purified by silica gel column chromatography (0-10% MeOH/CH2Cl2 gradient) to afford the desired product. LCMS-ESI+: calc'd for C30H31ClN3O3S: 548.2 (M+H+); Found: 548.3 (M+H+).

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-1ec2443a20084477aa1b1f081d252cef
出典メモuspto-grants-2015_03