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HRID 391331作成日:2026年10月26日

Methyl iodide → HCID 59578436、化合物

https://huagongshe.com/reaction/391331

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物3-Bromo-4-chloropyridineHCID 817696—
反応物Lithium diisopropylamideHCID 2724682—
反応物N-(cyclopropylmethylene)methanesulfonamideHCID 66788560—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 59578436HCID 59578436—

反応条件

温度-78 °C

反応手順

To a solution of DIPA (1.71 mL, 12 mmol) in THF (50 mL) at −78° C. was added 1.6M BuLi (7.5 mL, 12.0 mmol) and the mixture was stirred at −78° C. for 2 h. The LDA solution was cannulated into a solution of 3-bromo-4-chloropyridine (2.117 g, 11 mmol) in THF (50 mL) at −78° C., and the mixture was stirred at −78° C. for 1 h. A solution of N-(cyclopropylmethylene)methanesulfonamide (10 mmol, crude mixture) in THF (50 mL) was added and the mixture was stirred at −78° C. for 1 h. A solution of MeI (0.625 mL, 10 mmol) in THF (10 mL) was added, and the mixture was warmed to room temperature and stirred overnight. Water (0.5 mL) was added and the mixture was concentrated in vacuo. The residue was purified by silica gel chromatography eluting with a 0-50% EtOAc-heptane gradient to give N-((5-bromo-4-chloropyridin-3-yl)(cyclopropyl)methyl)-N-methylmethanesulfonamide. MS (ESI): m/z 353.0, 355.0 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383827B2
出典データセットuspto-grants-2013_02
ORD IDord-4d2480c9553a40798ecae9f1c0e51ad7
出典メモuspto-grants-2013_02