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HRID 38117作成日:2026年10月26日

Sodium hydride → Tert-butyl (trans)-2-(1,1'-biphenyl-4-yl)cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamate

https://huagongshe.com/reaction/38117

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2-Chloro-1-(4-methylpiperazin-1-yl)ethanoneHCID 818173—
反応物Tert-butyl(trans)-2-(1,1'-biphenyl-4-yl)cyclopropylcarbamateHCID 86658778—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl (trans)-2-(1,1'-biphenyl-4-yl)cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamateHCID 67448639—

反応手順

To a suspension of 1.5 equiv of NaH in dry DMF (10 vols) at 0° C. was added a solution of tert-butyl(trans)-2-(1,1′-biphenyl-4-yl)cyclopropylcarbamate derivative (1 equiv) in dry DMF (2 vols) and stirr for 30 mins. Then, added a solution of 1-(chloroacetyl)-4-methylpiperazine (1.5 equiv) in dry DMF (10 mL) at 0° C., stirred for 1 h at 0° C. to RT. The progress of the reaction was monitored by TLC. After completion, reaction mixture was poured into ice water and extracted with EtOAC. The combined extracts were washed with water, brine, dried over anhydrous Na2SO4, filtered and evaporated. The crude residue was purifying by preparative HPLC to get tert-butyl (trans)-2-(1,1′-biphenyl-4-yl)cyclopropyl(2-(4-methylpiperazin-1-yl)-2-oxoethyl)carbamate derivative

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524717B2
出典データセットuspto-grants-2013_09
ORD IDord-c32a277b93bd4a4fa6a6d77eca32ddec
出典メモuspto-grants-2013_09