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HRID 711575作成日:2026年10月25日

2-(Dicyclohexylphosphino)biphenyl → (R)-2-(4-(5-Cyanothiophen-2-yl)-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamide

https://huagongshe.com/reaction/711575

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Dicyclohexylphosphino)biphenylHCID 2734216—
反応物5-Cyanothiophene-2-boronic acidHCID 4198743—
反応物(R)-2-(4-Chloro-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamideHCID 58317560—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒DimethylformamideHCID 6228—
溶媒1,4-DioxaneHCID 31275—
生成物(R)-2-(4-(5-Cyanothiophen-2-yl)-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamideHCID 58317612—

反応条件

温度160 °C

反応手順

A solution of (R)-2-(4-chloro-2-(2,4-dimethoxybenzyl)-7-fluoro-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-6-ylamino)-4-methylpentanamide (114 mg, 0.245 mmol), 5-cyanothiophen-2-ylboronic acid (113 mg, 0.736 mmol), tris(dibenzylideneacetone)dipalladium(0) (13.47 mg, 0.015 mmol), and 2-(dicyclohexylphosphino)biphenyl (5.16 mg, 0.015 mmol) in dioxane (2 mL) and DMF (0.5 mL) was heated to 160° C. under microwave irradiation for 45 min. UPLC showed 50% conversion. The reaction mixture was subsequently heated at 160° C. under microwave irradiation for 45 min. Additional 5-cyanothiophen-2-ylboronic acid (113 mg, 0.736 mmol) was added and the reaction mixture was heated at 160° C. under microwave irradiation for 60 min. After removal of the solvent, the resulting crude material was reconstituted in MeOH/DMF (6.0 mL) and purified via preparative HPLC eluting with water (0.05% TFA) and ACN (40-80% gradient, 0.035% TFA). The collected fractions were stripped to dryness via rotary evaporation to yield the title compound. [M+H] calc'd for C27H28FN5O4S, 538. found, 538.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181255B2
出典データセットuspto-grants-2015_11
ORD IDord-c0308cf17a1745a1ba35182f4b7eae2a
出典メモuspto-grants-2015_11