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HRID 1042259作成日:2026年10月27日

Sodium Carbonate → 4-(2-fluoropyridin-3-yl)-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/1042259

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物2-Fluoropyridine-3-boronic acidHCID 2783270—
反応物7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
触媒HCID 178418397HCID 178418397—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物4-(2-fluoropyridin-3-yl)-7H-pyrrolo[2,3-d]pyrimidineHCID 5962737017%

反応手順

A mixture of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (7.68 g, 50 mmol), 2-fluoropyridin-3-ylboronic acid (10.57 g, 75 mmol), and tetrakis(triphenylphosphine)palladium(0) (2.89 g, 2.5 mmol) was suspended in DME (300 mL) and aqueous sodium carbonate (10%) (50 mL, 100 mmol). The suspension was heated at reflux over night, cooled to r.t. and the reaction mixture was partitioned between EtOAc (300 mL) and NaHCO3 (aq., sat., 200 mL). The aqueous layer was washed with EtOAc twice. The organic layers were combined and washed with brine, then loaded on silica and purified via flash column (EtOAc:hexane=50-95%) on ISCO to give 4-(2-fluoropyridin-3-yl)-7H-pyrrolo[2,3-d]pyrimidine as a light yellow solid with a green tint (1.85 g, 17% yield). MS (ESI, pos. ion) m/z: 214 [M+H]+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08557830B2
出典データセットuspto-grants-2013_10
ORD IDord-f56f02f51a004aaa8565503a101a2944
出典メモuspto-grants-2013_10