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HRID 216024作成日:2026年10月26日

Triethylamine → 1-(5-bromo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamide

https://huagongshe.com/reaction/216024

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物5-Bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidineHCID 5380710—
反応物N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamideHCID 67036908—
溶媒IsopropanolHCID 3776—
生成物1-(5-bromo-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamideHCID 57920204—

反応条件

温度100 °C

反応手順

To a solution of N-(3-(4-fluorophenoxy)phenyl)-4-methylpiperidine-4-carboxamide from example 1, step B, (36 mg, 0.1 mmol) in isopropanol (1 mL), was added to 5-bromo-4-chloro-7H-pyrrolo[2,3-d]pyrimidine from step A (24 mg, 0.1 mmol) and triethylamine (0.04 mL, 0.3 mmol). The reaction mixture was heated at 100° C. for 10 minutes under microwave condition, and then concentrated under vacuum. The product was isolated by prep HPLC to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193202B2
出典データセットuspto-grants-2012_06
ORD IDord-7fa5a5f9536446e1947c6ee98c1af544
出典メモuspto-grants-2012_06