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HRID 38251作成日:2026年10月26日

Triethylamine → Tert-butyl 4-(2-chloro-4-(picolinamido)phenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/38251

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Picolinoyl Chloride HydrochlorideHCID 135033—
反応物Tert-Butyl 4-(4-Amino-2-Chlorophenyl)Piperazine-1-CarboxylateHCID 18783766—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 4-(2-chloro-4-(picolinamido)phenyl)piperazine-1-carboxylateHCID 67441071100%

反応手順

According to Scheme 5 Step 3: Picolinoyl chloride hydrochloride (3.68 mmol, 656 mg) and Et3N (7.37 mmol, 1.03 mL) were added to a solution of tert-butyl 4-(4-amino-2-chlorophenyl)piperazine-1-carboxylate (2.46 mmol, 766 mg) in DCM (40 mL) at 0° C. The reaction mixture was stirred at room temperature for 1 hour. The organic phase was washed with a saturated solution of NaHCO3. The aqueous phase was extracted with AcOEt. The organic phase was washed with brine, was dried over Na2SO4, was filtered and was concentrated under reduced pressure to afford tert-butyl 4-(2-chloro-4-(picolinamido)phenyl)piperazine-1-carboxylate (2.46 mmol, 1.02 g, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524726B2
出典データセットuspto-grants-2013_09
ORD IDord-fbce41f4d7ee430591e03e6b74442165
出典メモuspto-grants-2013_09